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Aveng Grinaker-LTA are looking for young talented students who display leadership, innovative and practical qualities. Students from previously disadvantage backgrounds will be given preference. The bursary will be awarded to students studying towards a degree qualification within the following fields: Quantity Surveying Construction Management Civil Engineering Mechanical Engineering Mining Engineering  MORE ABOUT THE BURSARY PROGRAMME – COVERAGE VALUE The bursary will provide cover for the following expenses: tuition fees, prescribed textbooks, accommodation and a monthly allowance to assist with living expenses. Students will be required to undertake vacation work during university holidays.  ELIGIBILITY REQUIREMENTS Applicants must satisfy the following minimum entry criteria before applying (please note that failure to satisfy all the requirements will lead to your application not being considered): South African citizen OR South African permanent resident Completed Matric Studying full-time within one of the aforementioned fields of study Studying or have been accepted to study at a recognised South African university/ university of technology Passed Mathematics and Science in Matric Maintain a minimum of 65% overall average  HOW TO APPLY FOR THE BURSARY Download and complete the  Aveng Bursary Application Form   (.pdf)  Submit clear copies of the following supporting documentation along with your completed application form (the submission of these documents is compulsory – if any items are missing, your application be disregarded): ID document (certified copy) Matric certificate (certified copy) Latest tertiary results (certified copy) Testimonials (certified copies)  Applications must be submitted in one of the following ways: 1) Email: bursaries@aveng.co.za 2) Post: Group Talent Management Specialist 1 Jurgens Road Jet Park Boksburg 1459  CLOSING DATE 31 August 2019. (Applications open on 1 May each year.) (Applications submitted after this date will not be accepted – please apply before the closing date to ensure your application is considered.)  CONTACT THE BURSARY PROVIDER For any queries related to this bursary programme, please contact Aveng directly: Contact Person: Learning and Development Officer Tel: 011 779 2800 Email: bursaries@aveng.co.za

The FEDHASA Cape bursary is specifically for students entering their final year of study within the  Hospitality  field. FEDHASA Cape is made up of the Western Cape and Northern Cape Province. The bursary will cover full tuition fees to the maximum value of R70 000. Shortlisted applicants will be contacted by the FEDHASA Bursary Committee to attend an interview in September, and the outcome will be announced soon afterwards. If you do not receive any feedback regarding your application, please accept that it has been unsuccessful.  ELIGIBILITY REQUIREMENTS Applicants must satisfy the following minimum entry criteria before applying (please note that failure to satisfy all the requirements will lead to your application not being considered): South African citizen Completed Matric Completed your 1st and 2nd year of studies within the Hospitality sector, at a FEDHASA Cape member Training Institution Will be in your final year of studies in the upcoming year Passionate about working within the hospitality sector  HOW TO APPLY FOR THE BURSARY Download and complete the  FEDHASA Bursary Application Form  (.pdf)  Submit clear copies of the following supporting documentation along with your completed application form (the submission of these documents is compulsory – if any items are missing, your application be disregarded): ID document (certified copy) Curriculum Vitae Full academic record Letter of motivation (explaining why you should be awarded the bursary) Letter of recommendation from a lecturer or manager Proof of financial need (parents/ guardians proof of income: payslips if employed or affidavit if unemployed)  Applications must be submitted in one of the following ways: 1) Email: fedhasacape@fedhasa.co.za 2) Fax: 021 552 3466  CLOSING DATE 30 August 2019 (at 12:00). (Applications submitted after this date will not be accepted – please apply before the closing date to ensure your application is considered.)  CONTACT For any queries related to this bursary programme, please contact FEDHASA CAPE directly: Tel: 021 552 9870 Email: fedhasacape@fedhasa.co.za

Oasis bursaries will be awarded to students pursuing the following qualifications: Bachelor of Business Science (BBusSc) – specialising in: Analytics/ Economics/ Economics with Law; Marketing; Organisational Psychology/ Finance/ Quantitative Finance/ Finance with Accounting/ Computer Science/ Information Systems (as well as Postgraduate students in one of the above) Bachelor Of Commerce (Bcom) – specialising in: Actuarial Science/ Actuarial Science specialising in Quantitative Finance/ Financial Accounting: General Accounting/ Financial Accounting: Accounting with Law/ Financial Accounting: Chartered Accountancy/ Economics and Finance/ Economics with Law/ Economics and Statistics/ Philosophy, Politics and Economics/ Management Studies/ Organisational Psychology/ Industrial Psychology/ Human Resource Management/ Information Systems/ Information Systems and Computer Science/ Bcom Law/ Bcom Economics with Law/ Bcom Financial Accounting with Law/ BAcc LLB (as well as Postgraduate students in one of the above) Bachelor of Science (BSc) – specialising in: Construction Studies and Property Studies (as well as Doctor of Science (DSc) degrees in one of the above) Bachelor Degree – specialising in: Quantity Surveying/ Town and Regional Planning/ Operational Management/ Btech Construction Management and Quantity Surveying (as well as Doctor of Science (DSc) degrees in one of the above) Bachelor of Science Honours (BScHons) – specialising in: Quantity Surveying/ Property Studies/ Geographical Information Systems (as well as Doctor of Science (DSc) degrees in one of the above) Masters degree – specialising in: Property Studies/ Project Management (as well as Doctor of Science (DSc) degrees in one of the above) Law degrees and diplomas, including the following: Postgraduate Diploma (PGDip) (Regulatory Compliance Management) Master of Laws (LLM) – specialising in: Labour Law/ Commercial Law/ Contractual Law/ Tax Law/ International Trade Law/ Intellectual Property Law Master of Philosophy (MPhil) Doctor of Laws (LLD) Doctor of Philosophy (PhD) Bachelor of Science (BSc) – specialising in: Mathematics/ Applied Mathematics/ Mathematical Statistics/ Applied Statistics/ Business Computing/ Computer Science/ Computer Engineering/ Information Technology/ Information Systems/ Masters in Information Systems Bachelor of Science Honours (BScHons) & Master of Science (MSc) – specialising in: Mathematics/ Applied Mathematics/ Mathematical Statistics/ Decision Sciences & Analytics/ Operational Research/ Computer Science/ Computational Science/ Information Technology Bachelor of Arts (BA) & Bachelor of Social Science (BSocSc) – majoring in: Economics/ International Relations/ Statistics/ Industrial Sociology/ Psychology/ Organisational Psychology/ Philosophy, Politics and Economics/ Mathematics/ Applied Mathematics/ Mathematical Statistics/ Applied Statistics/ Computer Science/ Film and Television Studies/ Audiovisual Production Management/ Visual Communications (Graphic, Illustrations & Photography, Digital)/ Media and Writing/ Multimedia Design/ Graphic Design/ Digital Marketing/ Web Design/ Strategic Brand Communications/ Copywriting/ Brand Building and Management/ Strategic Brand Management  MORE ABOUT THE BURSARY PROGRAMME – SERVICE CONTRACT & SELECTION PROCESS Bursary recipients are required to take part in the Vacation Work Programme. Once students have graduated, they must take up employment at Oasis – the working period will be equal to the duration of funding received as well as 1 extra year.  Applicants will receive acknowledgement of their application within 2 weeks of applying – if you do not receive any receipt of confirmation, you should contact the Bursary Officer (021 413 7860). Successful applicants will be notified of the outcome of their application by 31 December 2019 at the latest. Successful applicants who wrote their Matric exams will be notified of the outcome of their application as soon as possible after your final matric results are received. If you do not receive any feedback (other than the receipt of confirmation), please regard your application as unsuccessful.  ELIGIBILITY REQUIREMENTS Applicants must satisfy the following minimum entry criteria before applying (please note that failure to satisfy all the requirements will lead to your application not being considered): South African citizen Completed Matric OR currently in Matric Studying or intending on studying full time in one of the aforementioned fields of study Studying or intending on studying at a recognised tertiary institute in South Africa NOT in receipt of any other bursary funding or another type of financial assistance from any other company  HOW TO APPLY FOR THE BURSARY Download and complete the  Oasis Bursary Application Form  (.pdf)  Submit clear copies of the following supporting documentation along with your completed application form (the submission of these documents is compulsory – if any items are missing, your application be disregarded): ID document OR passport (certified copy) Colour photo (passport size) to be attached to the top right corner of the first page Full academic record from Grade 10 to present, if currently in Matric (certified copies) Full academic transcripts AND certificates to date (including Matric, A level, O level/ Bachelors, Honours, Masters and PhD) (certified copies) Acceptance letter OR preliminary acceptance letter from your selected tertiary institute Bursary or Loan Agreement Tax Invoice stating the tertiary institutes fees Testimonial if applicable, from one of the following: your Teacher, Principal, Lecturer, Faculty Dean Proof of household monthly income Proof of any dependents Monthly budget, stating income and expenses Medical certificates Curriculum Vitae 2 minute video (further instructions can be found on page 5 of the application form) Letter of recommendation from a parent or guardian (optional)  Please note: If applicants are unable to submit a supporting document, they must provide an explanation as to why they cannot provide it. They must also state when the outstanding documents will be submitted. Documents must be arranged in the order as stated on page 6 of the application form.  Applications must be submitted online via WeTransfer (https://wetransfer.com/) (this is a free service – documents must be compressed into a single PDF file) Applications must also be hand delivered to your nearest Oasis office: Cape Town: The Bursary Officer Oasis Crescent Fund Trust Oasis House 96 Upper Roodebloem Road, University Estate Cape Town 7925 Johannesburg: Oasis Crescent Fund Trust 4th Floor, West Office Tower Nelson Mandela Square Sandton Johannesburg 2146 Durban: Oasis Crescent Fund Trust Shop 49, The Ridge@Shallcross 90 Shallcross Road Chatsworth Durban 4134  CLOSING DATE 29 August 2019. (Applications submitted after this date will not be accepted – please apply before the closing date to ensure your application is considered.)  CONTACT THE BURSARY PROVIDER For any queries related to this bursary programme, please contact Oasis directly: Contact Person: Bursary Officer Tel: 021 413 7860 Tel: 021 413 7923 (Cape Town) Tel: 011 263 7860 (Johannesburg) Tel: 031 409 0786 (Durban) Email: bursary@oasiscrescent.com

ERC provides governance, portfolio and programme management expertize, as well as administrative support to the regional change agenda, thereby ensuring seamless end to end delivery, prioritised execution against detailed requirements and the efficient use of our resources.  ERC activities also directly support our regulatory communications strategy through a UK and Ireland Regulatory Affairs function.  Activities include: Coordination and management of the Regional Change Portfolio, inclusive of budgeting and resourcing. Consolidated reporting and communications. Programme initiation and set up. Change delivery across the Corporate portfolios (Strategic Growth and Change, Sustain/Support Current Business Model and Regulatory Control). Remediation and fix of failing programmes. Provision of an ERC Regulatory Affairs function supporting regulatory communications.  Background to Role :  Consults with stakeholders of all levels of the organisation to analyze, define, and prioritize business requirements and functional and operational specifications for a functional work stream.  Formulates and defines program scope and objectives for the work stream with thorough understanding of business processes in a specific business domain.  Represents the business to all areas in resolving issues and developing both business and technology solutions.  May lead staff on specific projects.     Business Analyst Duties : Elicits, challenges, and prioritizes business requirements; translates into functional design and use case models. Develops project scope and identifies objectives, constraints, issues, risks and assumptions for large programmes, and escalates as necessary. Is accountable for overall delivery of assigned functional workstream on a large-scale programme. Aligns resources, seeks input from key constituents, and manages others to achieve desired results. Provides guidance on development of the functional requirements and user documentation. Assists in developing implementation/conversion strategy and implementation plan. Manages scope and change throughout the initiative utilizing formal change control and requirements traceability. Gathers and analyzes information and develops recommendations to address major business objectives that span multiple, global business and technology areas.  Information gathering may require the ability to handle and analyze large scale data across multiple systems and products. Develops process and workflow maps as necessary, recommending enhancements needed to procedures and controls.  Works with business and technology teams to develop technology roadmap strategy when appropriate. Ensure deliverables are completed on time, within budget and with minimum defects. Adhere to methodologies adopted by the Firm and ensures a smooth transition of product knowledge to all relevant parties in business as usual including business partners for approval. Conduct status meetings and facilitate issue resolution and risk mitigation.  Provide Programme level reporting to senior staff. Coordinate and manage scoping of assigned data fields to inform effective business decision making; leading the business and operations teams to remediate gaps in identified data fields. This will include scheduling, preparing and running workshops as needed. Recording actions, decisions and assumptions, and inputting data into the programme traceability tool. Provides technical consultation concerning business implications of complex application development projects. Supports testing of new or enhanced applications and/or systems and provides guidance to junior team members on complex testing tasks including case development, requirement traceability analysis, test preparation, script writing, and functional test execution. Uses deep expertise and broad knowledge of regulatory and legal requirements, and BNY Mellon corporate policies involving risk and control, to support the development of improved business processes. May lead a small team on moderately complex projects. Qualifications Education/Qualifications : Bachelor's degree in business or technical-related discipline, or equivalent work experience required. Formal project management qualification; six sigma and experience in Agile methodologies is advantageous Good knowledge of custody, operations, technology change and related business activities. A depth of experience in data management and reporting; process and workflow mapping; writing and managing business requirements and functional specifications. Knowledge and experience of working within the regulatory environment, and how that impacts (BNY Mellon) Business areas Strong judgment and leadership skills combined with the ability to work independently with minimal supervision. Strong planning and project organization skills.  Strong negotiation, decision making, problem solving and influencing skills.  Ability to effectively prioritize and multi-task in a high pressure, high volume environment. Ability to run both small and large scale workshops and working groups with varying levels of stakeholder seniority. Ability to analyse medium to large scale data and information across multiple sources. 8-10 years of experience in managing senior stakeholders First class communication skills, both verbal and written. Literacy in the following software packages: Outlook, Word, PowerPoint, Excel (high level of skill essential), Visio, Project (latter not essential) , Access (advantageous, not essential) Flexibility in terms of both working hours and work undertaken will be required.

Cancer Vaccines & Immunotherapeutics seeks to discover novel vaccines for the prevention and treatment of significant human diseases, using a variety of vaccine technology platforms in combination with immunomodulatory agents. We are searching for a motivated individual with a basic scientific understanding of immunology with some experience in theory and laboratory practice of one or more or the following laboratory immunoassay techniques: serology-based antibody assessment (ELISA, Luminex, hemagglutination inhibition, flow cytometry-based cell binding assays), cellular immunology-based culturing of immune cells, cellular immunoassays, e.g.ELISpot, and flow cytometry-based intracellular cytokine staining of T cells. The candidate will be required to proactively apply their knowledge to prosecute experimental work plans provided by their supervisor and effectively conduct their work semi- independently and as a member of the Immunology team. The candidate will be required to summarize and critique their results, with guidance from their supervisor, as well as on occasion communicate data effectively at work-group meetings.   This role is primarily laboratory based with a major emphasis placed upon implementing state-of-the-art immunologic techniques, and routinely conducting high-quality assay work in an organized and safe manner.  ROLE RESPONSIBILITIES Laboratory and related work (~90% of time) with supervision: Understand study aims and experimental plans provided by supervisor and follow detailed SOPs to run a variety of serology or cell-based immunoassays (including studies with large sample numbers >100). Assist with flow cytometry assays for immune cell profiling (ICP) and intracellular cytokine staining (ICCS). Perform cell culture to maintain the viability and sterility of multiple immortal cell lines. Using standardized methods, analyze experimental data and with support of supervisor generate data summaries for interpretation by the vaccine project teams. Regularly record experimental work upon completion in electronic notebook systems and archive instrument raw data in server databases. Identify and report any experimental problems, troubleshoot causative factors, and suggest necessary corrections in discussion with supervisor. Support general laboratory operations including daily preparation of buffers and solutions, ordering and re-stocking laboratory supplies, and maintaining a clean work environment and maintenance of equipment.  Communication: Actively participate in discussions at work-group meetings and contribute ideas at Immunology line meetings. Provide timely responses to project team requests for data and information. Develop clear and concise presentation skills by presenting data summaries at internal meetings. Safety: Comply with all EH&S regulations and safe laboratory practices. Identify and act to reduce hazards and risks in the laboratory through use of risk and hazard assessments.  QUALIFICATIONS Bachelor of Science in life sciences, preferably including coursework in biology and immunology. Minimum 1 year experience in a relevant laboratory setting that routinely performs biological or immunological assays Preferred: Prior work experience in biotech/pharmaceutical industry settings Practical experience with the processing of murine and/or human tissue and blood samples  NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS This is a 1st Shift position  Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.  EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.  Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Pfizer is an E-Verify employer.  ADDITIONAL OFFER DETAILS Eligible for Employee Referral Bonus: Yes​

You will be a cutting-edge research engineer, working closely with surgeons and surgical specimens to adapt custom software and hardware to transform our academic prototype into a product prototype. The position will entail software development --primarily in Matlab—to drive a multi-laser engine in multimodal imaging. A comfort with, and basic understanding of, mechanical and electronic-circuit design, alongside fabrication methods (milling, lathing, etc.) is expected. Experience in optics/microscopy required. Knowledge of basic tissue staining procedures and optics/laser alignment a plus. Must be able to work both independently and closely with the inventor to accomplish a complete product prototype, from design through fabrication and testing. SurgiVance extensively uses opto-mechanics in reflectance mode confocal microscopy and fluorescent stains for molecular labeling of multiple tissue components. Specific initial responsibilities include:  Opto-mechanically re-designing the prototype to remove the current laser illumination system and inserting the new multi-laser engine  Performing experimental imaging that quantifies the resolution and contrast performance parameters of the imaging system.  Imaging discarded surgical specimens and creating a user interface to do so efficiently and in an organized way that permits comparison of the imaging results to gold standard pathology.  Working closely with multiple surgeons to analyze and ameliorate the pain points and to supercharge the interactive pathology experience between the technology and user.  Depending on expertise and interest, other projects may involve design and manufacturing of specimen compression chambers, biochemistry of molecular label formulation in tissue staining to optimize imaging contrast, design of deep learning algorithms to execute pathological analysis automatically, integration engineering with medical informatics, etc.  Performing complete project cycles, from design to fabrication, with support from a small engineering core in the university’s fabrication and machining facility.  You Have   A Bachelor's degree (or higher) in engineering, math or physics.  Knowledge of optics, lasers, microscopy, or other medical imaging experience. A willingness and ability to rapidly assimilate new fields of knowledge, from machine vision algorithms to electronic circuit design, for the purpose of building functional pathology systems or completing medium-sized coding projects.  The ability to clearly communicate engineering principles, design and coding with surgeons and the capacity to work collaboratively with members of the startup company to optimize systems and coding as clinical needs require.  The ability to multitask and assist in the design and optimization of different systems simultaneously to support the development of the product prototype toward the final, frozen design that will go into multicenter FDA clinical trials.  You Are   Experienced writing code in multiple languages including Python, C++, and Matlab and comfortable designing and building mechanical and electronic devices  Excited by the opportunity to rapidly assimilate new information for the purpose of solving design challenges in pathology and medical informatics.  Detail-oriented, accurate, and precise  Capable of working both independently and within a small team  Creative and enjoy the iterative process of design development 

PPD is a leading global contract research organization.  At PPD we are passionate, deliberate, and driven by our purpose - to improve health!   PPD Laboratories offers the most comprehensive set of laboratory services available in the industry.  Our scientists work together to accelerate pharmaceutical development for small molecules, biologics, and vaccines -allowing our clients to make faster decisions about their compounds.    As an Associate Research Scientist you are committed to excellence and high quality results in your complex laboratory analysis of key pharmaceutical products. Beyond the bench, you work as a project leader with a strong sense of urgency aligned to our customers, and you are committed to delivering results. Responsibilities: Independently performs analytical testing, method optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems. Understands and conforms to methods,and protocols applicable to assigned tasks.  Designs and executes experiments independently Reviews and critiques study protocols, project status reports, final study reports and other porject-related technical documents Prepares and reviews study protocols, project status reports, final study reports and other project-related technical documents Communicates data and technical issues to clients as needed Leads analytical (procedural and instrumental) trouble shooting sessions PPD offers continued career advancement as a Scientist, as well as management and specialized opportunities in other departments within PPD.  At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It's not just talk, our award-winning training programs speak for themselves. To learn how PPD can advance your career, apply now! What To Expect Next We are looking forward to receiving your application. A member of our talent acquisition team will review your application and if interested, you will be contacted for an interview.  Qualifications Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable 5 years) or equivalent combination of education, training, & experience.  Knowledge, Skills and Abilities:  Knowledge of GMP Microbiology testing and requirements Knowledge and use and maintenance of cleanrooms and barrier isolator systems Ability to independently perform root cause analysis for method investigations Proficiency on technical operating systems Proven problem solving and troubleshooting abilities Proven ability in technical writing skills Time management and project management skills Good written and oral communication skills Ability to work in a collaborative work environment with a team Ability to train junior staff PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.  Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner Able to work upright and stationary and/or standing for typical working hours Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments Able to use and learn standard office equipment and technology with proficiency May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments Able to perform successfully under pressure while prioritizing and handling multiple projects or activities

Essential Job Duties and Responsibilities Contributes to development of new concepts from initial design to market release. Contributes to execution of established Design Verification test protocols. Conducts feasibility studies of the design to determine ability to function as intended. Maintains detailed documentation throughout all phases of product development. Contributes to risk analysis for products under development. Coordinates activities with outside suppliers and consultants to ensure the delivery of supplies or services needed to meet scheduled timelines. Participates in client meetings.  Proactively communicates with team to ensure an ongoing two-way exchange of information. Any other duties as assigned. Education and Experience Requirements Bachelor's degree in Mechanical, Plastics or Biomedical Engineering is desired.  In lieu of a degree, previous experience in a similar or exact role may be considered. 0 – 2 years of medical device design and development experience is desired. Skills and Abilities Ability to interact with clients and companies in a professional manner. Customer focus with proficient communication skills, written and oral. Flexibility, persistence, resourcefulness, a drive to succeed, and an entrepreneurial spirit. SolidWorks 3D CAD proficiency. Familiarity with Design for Manufacturability and Assembly (DFM / DFA) is desired. Some experience working with operations to develop strong manufacturing process instructions and operator training to ensure smooth product transition into the manufacturing environment is desired. Familiarity with FDA QSR and ISO 13485 medical device regulations is desired. Familiarity with probability and statistics. Working Conditions and Physical Demands To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

This opportunity is an experience that you will live in the Digital world. You will be facing consulting and project management realities, learning while working in a highly professional environment. If you feel a deep passion for customer delivery, innovation and the ICT Industry, if you are an early adopter or digital community leader, if you enjoy using the latest technologies, this is where you want to be.  If you are: Adaptable, flexible, agile Effective communicator, you influence others Able to experiment “outside the box” Technical & business orientated A potential leader A business & change driver Strategic analyst  You will be: As part of our 2019 programme, we have a number of roles that require individuals either graduating this year or with a recent degree in either a technical or business focused degree along with a post graduate degree in Project Management. Initially you will support senior Project Managers in all aspects of project delivery however after a short time, you will pick up your own projects and deliver these within a project environment to our customers, these will be both internal and external projects.  We are looking for customer focused individuals who want to become part of an organisation who are committed to developing those with talent and a passion for all things project related. We can offer a very real opportunity for you to grow your knowledge and make your mark on some exciting projects.  To be part of this journey you should: Be a recent graduate or graduating this year with a masters’ degree in Project Management Some work experience is a bonus although not essential Strong communication and presentation skills Excellent customer service skills  Apply and fasten your seatbelt… You are about to start an exciting journey!

AECOM is actively seeking a highly motivated Entry Level Aviation Engineer for employment in the Philadelphia, PA office. AECOM is pleased to include you in a unique development opportunity, the Graduate Development Program (GDP). This program is designed to support your assimilation into the organization and assist with creating a foundation of knowledge for a successful career at AECOM. You will gain experience in your discipline through learning on the job and participate in development opportunities during the program, including access to AECOM's social media resources, group mentoring, and professional networking. The program also has learning activities that will be available to you, including webinars and on-line programs. Imagine working on rewarding projects within a diverse culture, and having access to exceptional training and career development opportunities. Working at AECOM means being part of a global team, working with award-winning professionals across the world. Aspire to be a key player on some of the best projects regionally, with opportunities to work on projects nationally or internationally. Our people bring deep industry knowledge to help you succeed. The responsibilities of this position include, but are not limited to: Builds analytic and design skills Conducts engineering design under the supervision of an experienced engineer Creates designs, calculations, sketches, diagrams, schematic drawings, and final working drawings under the supervision of an experienced engineer Collects and analyzes data under the supervision of an experienced engineer Uses computer software as a tool for solving basic engineering problems Performs work in accordance with agreed upon budget and schedule under supervision Minimum Requirements Bachelor's degree in related field Preferred Qualifications None What We Offer When you join AECOM, you become part of a company that is  pioneering the future  . Our teams around the world are involved in some of the most cutting-edge and innovative projects and programs of our time, addressing the big challenges of today and shaping the built environment for generations to come. We ensure a workplace that encourages growth, flexibility and creativity, as well as a company culture that champions  inclusion, diversity  and overall  employee well-being  through programs supported by company leadership. Our  core values  define who we are, how we act and what we aspire to, which comes down to not only  delivering a better world  , but working to “make amazing happen” in each neighborhood, community and city we touch. As an Equal Opportunity Employer, we believe in each person’s potential, and we’ll help you reach yours.

The Engine Oils Product Development Engineer/Scientist is to build our core competency and develop lubricants for Passenger Cars and Heavy-Duty Diesel Engines. The demand for the engine lubricants with better fuel economy and durability has been rapidly growing over the years.  This position is critical in understanding the technical needs of key customers and Original Equipment Manufacturers (OEMs) and translating those needs into a profitable, efficient product development.  This position requires a thorough understanding of lubricant technology and is expected to work with cross-functional teams including Brand, Product Technical Services, and regional sales.   Responsibilities for this position may include but are not limited to: Develops engine oils for Chevron Lubricants in alignment with sector, segment and product line strategies. Applications include on- and off-highway diesel trucks/equipment, natural gas engines, passenger cars, motorcycles, inland marine and railroad engines.  Specific area of work will be based on the successful candidates experience and business needs. Applies project management skills. Understands the needs of customer, engine manufacturer, and industry requirements. Develops well-defined, well-planned programs with stage-gates, timelines, and budget targets. Interprets data and test results and draws conclusions against project objectives/requirements. Communicates technical program results, benchmarking information and conclusions. Manages base oil changes and leverages our global experience with equity and non-equity base oils. Develops strong relationships with additive suppliers to assess their technology options/capabilities and with major OEMs to determine their current and future lubricant needs Defends the brand. Works effectively with Brand Management and Technical Support functions to understand and address field problems and communicate Chevron position to customers and OEMs. May represent Chevron at industry technical meetings such as American Society of Testing and Materials, API, Society of Automotive Engineers and others. Reinforces the Chevron Way values.  Required Qualifications: BS Degree in Mechanical Engineering, Materials Science, Chemistry, Chemical Engineering Minmum 5 years experience/knowledge of Lubricants or Lubricant Additives and Experience in the Lubricants or Lubricants Additives Industry with an understanding of tribology, fundamentals of lubrication, additive chemistry and internal combustion engine operation, design, or maintenance Project Management/Leadership:  able to set priorities to meet business objectives while being flexible to manage changing priorities; can work on multiple projects concurrently; can work independently while keeping key stakeholders aware of critical decision points; capable of driving a diverse team to project completion in line with business needs and timeline Teamwork:  demonstrated ability to work effectively and cooperatively with technical, product management, and marketing personnel from diverse backgrounds in a team environment. Communication:  ability to communicate effectively across varied disciplines in a clear and concise manner:  orally, written, presentation Analytical and Problem-Solving Skills:  ability to understand complex issues, analyze data and then develop appropriate solutions/conclusions Creativity and Innovation:  has a proven track record of translating a basic idea or concept into a well-laid-out test plan, designed to generate the data to demonstrate a performance differentiation  Preferred Qualifications: Advanced degree in Mechanical Engineering, Materials Science, Chemistry, Chemical Engineering  Relocation Options:  Relocation  may be  considered. International Considerations:  Expatriate assignments  will not be  considered. Chevron regrets that it is unable to sponsor employment Visas or consider individuals on time-limited Visa status for this position.  Regulatory Disclosure for US Positions:   Chevron is an Equal Opportunity / Affirmative Action employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status, or other status protected by law or regulation.  Chevron participates in E-Verify in certain locations as required by law.

The Manufacturing Sciences department within the Operations Science & Technology organization leads the optimization, validation, implementation, continuous improvement and global technical support for late stage and commercial manufacturing of therapeutic proteins for AbbVie. We have an exciting opportunity for an Associate Scientist I position, Cell Culture based in Worcester, MA.  Key Responsibilities: Executes experiments in process development and manufacturing support with supervision. Performs basic data acquisition and analysis in a timely manner. Assists in experimental designs and data interpretation. Documents work appropriately in lab notebooks and technical memos; contributes to writing technical reports Maintains lab equipment and optimizes lab operations for efficient use of time and resource. Troubleshoots equipment and experimental problems. Assists in continuous improvement activities. Assists in manufacturing support.  Key AbbVie Competencies: Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance. Learns fast, grasps the 'essence' and can change the course quickly where indicated. Raises the bar and is never satisfied with the status quo. Creates a learning environment, open to suggestions and experimentation for improvement. Embraces the ideas of others, nurtures innovation and manages innovation to reality. Qualifications BS degree in a scientific or engineering discipline Understands basic scientific/engineering principles applicable to assigned tasks. Capability to consult literature/reports or other independent research to understand and develop scientific purposes of assignments. Is familiar with routine statistical methods and has the ability to apply these methods to experimental data. Has demonstrated ability to identify critical information from own work and has also contributed to experimental design. Good communication and scientific skills, the desire and drive to grow and develop scientifically. Ability to work effectively in a highly collaborative and dynamic environment. Strong sense of urgency and self-motivated desire to achieve. Must have a “results-oriented” work ethic and a positive, “can-do” attitude. Preferred: Previous biopharmaceutical industry experience within relevant scientific discipline. Mammalian cell culture experience with media preparation, operation of shake flasks and bioreactors and relevant cell culture analytical techniques. Prior experience with manufacturing support and knowledge of process development. Additional Information AbbVie is an Equal Employment Opportunity employer: At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. Significant Work Activities and Conditions: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Looking for a place to start your career? A place where you can work with industry recognized professionals who are solving tough environmental problems? Geosyntec is the place for you! As an  Entry-Level Analytical Measurement Engineer or Scientist  in our air and water analytical measurements, methods development, and field service practice in  Knoxville, Tennessee,  you will have the opportunity to apply your academic knowledge to real-world situations while also learning the business skills needed for a successful consulting career. Our clients ask us to address their new ventures and most challenging problems involving the environment, natural resources, and civil infrastructure. Ranked by ENR in the top 20 design firms for the environment, Geosyntec is internationally known for its technical leadership, broad experience, and exceptional client service. Learn more by visiting  www.geosyntec.com . ABOUT THE POSITION: Is this the right position to help you achieve your professional goals? Some of the key responsibilities for the Entry-Level Analytical Measurement Engineer or Scientist position include: Hands-on laboratory usage and field deployment of various types of optical monitoring equipment; Custom design and assembly of optically based trace gas/water detection systems, including method development, maintenance and troubleshooting; Data processing, data quality assurance and control, data review and interpretation from the operation of optical instrumentation including FTIR, Raman, LIBS, extractive UV, UV-DOAS, Tunable Diode Laser and various LED absorption assemblies; Assist in the designing and writing of technical client proposals; Fieldwork such as instrument set-up, sample or materials analysis, and data acquisition; Data analysis, including interpretation of spectral data and preparing, tables, and figures; and Preparation of technical reports, letters, memoranda, plans, specifications, and proposals. You should expect to work closely with experienced professionals who will guide and integrate you into Geosyntec’s culture, as you kick start your career. Here are some other things you should know about a typical Entry-Level Analytical Measurement Engineer or Scientist position with Geosyntec: Training : This position requires OSHA health and safety, first aid, and CPR training and medical monitoring, paid for by the firm. We also offer professional development opportunities including in-house seminars, webinars, and mentoring, that allow our professionals to build the technical and business skills necessary to become successful consultants Fieldwork:  Up to 30% Overnight travel:  Up to 30% Your success is our success. We encourage our professionals to continually develop their interests and skills. Advancement is based on an individual’s own performance and initiative. CANDIDATE QUALIFICATIONS: BS degree in electrical or mechanical engineering, chemistry, or physics. (required) Advanced degree with an experimental thesis in electrical or mechanical, chemistry, or physics. (preferred) Academic laboratory experience in design/development of optical measurement instrumentation, calibration methods, and quality assurance/quality control procedures. (required) Experience in quantitative analyses of trace level contaminants in water and/or air. (preferred) Extensive training in optical spectroscopies (especially in the infrared and ultraviolet). (preferred) Experience in the analysis and interpretation of spectral data. (required) Practical knowledge of laser safety and laboratory chemical hygiene. (preferred) Coding for instrument control and data acquisition. (preferred) Valid driver’s license and a satisfactory driving record. (required)                                                 WHAT DOES IT TAKE TO BE SUCCESSFUL AT GEOSYNTEC? Geosyntec strives to hire and retain the best and brightest people in their fields. We look for exceptional interpersonal skills, communication skills, and problem-solving abilities, plus the passion for technical excellence and quality. We seek individuals with leadership potential, a commitment to lifelong learning and growth, and the desire to build a long and rewarding career with a growing Firm. WHY CHOOSE GEOSYNTEC? Geosyntec is a great place to build a career. If you're looking for an exciting place to work, a place with challenging and rewarding projects, and a place that has been nationally recognized for its employees' quality of life, technical expertise, and business success, then Geosyntec may be the place for you.  We are proud to offer our employees a highly competitive benefits package.

The Associate Research Engineer will work under the direction of the group lead with the primary role of electrolyte formulation preparation, assembling and testing small electrochemical vehicles to evaluate battery materials. This individual will be required to operate software used to program and run the battery testing instrument, as well as to process and report test data in a standardized format. The Associate Research Engineer will also be responsible for preparing powder samples for analysis, and performing tests to measure their physical properties. Support may also be required for evaluation of electrolytes and separators. Results and data analysis will be summarized in written reports and maintained in laboratory notebooks and intranet locations.  Primary Responsibilities Electrolyte formulation preparation and evaluation Assembling and testing of electrochemical test vehicles to evaluate battery materials Processing, recording and tracking test data using certain software tools Preparing electrode for multi-layer cell building Conduct electrochemical cell teardown and failure mode analysis with analytical techniques Conduct testing of cells made with various electrolytes to assess gas volume and expansion Manage inventory of R&D chemicals, and monitor safety practices in the lab Performing other functions as required to support the R&D operation  Qualifications Specific Skills/Abilities Attention to detail Ability to work with a minimum amount of supervision. Proficiency with Microsoft excel and have some mechanical aptitude. Ability to work with analytical balances, some chemicals, and general lab-ware is necessary General lab skills, as well as ability to learn instrumentation software are a must. Education/Experience Bachelor’s degree required. Demonstrated ability to perform various math calculations and use test / measuring devices. Experience working with glove boxes and dry room is preferred. Experience with batteries or electrochemical systems a strong plus Familiarity with Statistical Process Control, and Design of Experiments a plus  A123 is an equal opportunity/affirmative action employer Additional Information All your information will be kept confidential according to EEO guidelines.

Responsible for full life cycle development of Class I and II medical devices, which includes initiation, design, development, execution, verification/validation, release, and product maintenance.  Recognized as key technical resource.   ESSENTIAL DUTIES AND RESPONSIBILITIES:   Support team efforts in establishing program design inputs and/or requirements, ensuring compliance to Arthrex QMS and global standards and regulatory requirements Manage completion of Design Control Documentation: Traceability Matrix; Risk Management File; Verification and Validation Plans and Protocols; etc. Support team efforts in product complaints review, root cause failure analysis activities Support team efforts to develop, track and monitor functional systems needs and reliability throughout a products life cycle, making recommendations on corrective actions and/or potential enhancements. Develops and manages product compliance initiatives to relevant standards governing medical electrical equipment. Supports the execution of engineering changes, lifecycle changes and/or document changes prior to release. Supervises, assigns and/or coordinates scope and breadth of quality/regulatory testing to be performed to ensure compliance to all ISO and regulatory standards required for a given product or assignment Supports Quality System Audits conducted by external agencies, such as FDA, Notified Body and/or Regulatory Agency audits. Contributes to efficient and effective program management Ensures alignment of internal and external customers. Some required travel to attend trade shows and visit established accounts as well as prospective accounts. International travel may be required.   Incidental Duties: The above statements describe the general nature and level of work being performed in this job.  They are not intended to be an exhaustive list of all duties, and indeed additional responsibilities may be assigned, as required, by management.   Education and Experience: Bachelor’s degree in Engineering required; preferably in Biomedical, Electrical, Mechanical, or Chemical Engineering. Experience in medical device product development or similar environment preferred.    Knowledge and Skill Requirements/Specialized Courses and/or Training: Experience with full medical device product development cycle preferred. Strong strategic thinker, excellent collaboration and communication skills, careful attention to detail Ability to balance business and technical risks while remaining compliant with internal systems. Working knowledge of medical device regulations and associated quality systems, particularly design controls and risk management. Understanding of Design for Manufacturability, including manufacturing process optimization support, and Design for Cost. Understanding of Design for Quality with tools such as FTA, FMEA, etc. Manufacturing process knowledge preferred. Awareness orthopedic surgery principles, theories, and products preferred Knowledgeable of FDA and ISO guidelines for the development of medical devices required. Technical knowledge in development methodologies, design and test in support of program release. Ability to confidently lead and/or support complex, cross functional teams independently. Continuously seeking ways to improve complex systems of people, processes and/or technologies.  Machine, Tools, and/or Equipment Skills: Experience with electrical medical equipment and accessories development and testing. Understanding of regulatory standards for technical specialty areas as electrical, mechanical, software, chemical and data transfer design standards.  Knowledge of surgical equipment and instrumentation, mechanical testing equipment, SolidWorks or other 3D modeling software.  MS Office, PC and Databases.   All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

A global leader in consulting, technology services and digital transformation, Capgemini is at the forefront of innovation to address the entire breadth of clients'​ opportunities in the evolving world of cloud, digital and platforms. Building on its strong 50-year heritage and deep industry-specific expertise, Capgemini enables organizations to realize their business ambitions through an array of services from strategy to operations. Capgemini is driven by the conviction that the business value of technology comes from and through people. It is a multicultural company of 200,000 team members in over 40 countries. The Group reported 2018 global revenues of EUR 13.2 billion.  People matter, results count. Who you’ll be working with The Capgemini Operational Technology (OT) Security team has been established for over 14 years providing consultancy services to our customers in order to help them understand the existing security posture of their OT environment identifying where potential gaps or vulnerabilities exist.  Our team then works with our customers to intro  Due to growing customer demand, we are currently looking to recruit a Cyber Security Consultant to join our team of Consultants and Engineers who will share their experiences of working in a rapidly changing, and prominent, area of business in order to take your career to the next stage. The Focus of your role Conduct consultancy and project management assignments in the field of Operational Technology (OT) Security to help customers mitigate the risks of vulnerabilities in their OT environment. This candidate should have excellent communication skills, both written and oral, and the ability to interact with others from the executive level down to highly technical analysts in structured and unstructured situations.  What you’ll do Conduct site surveys to help customers identify the systems in their OT environment (including offshore environments) Conduct system and network security compliance assessments to assess vulnerabilities in OT environments Facilitate risk assessments to assess and mitigate the identified vulnerabilities in OT environments Develop OT policies and procedures to help customers reduce the risk of a security breach at an installation, and sustain OT security Conduct audits and gap analysis to assess customer compliance against policies and procedures to ensure on going protection against security incidents Remediation of OT to close gaps and ensure compliance with policies and standards Provide general OT security advice to assist customers addressing OT security issues and ensure safe, continuous production operations Resolve customer issues What you’ll bring Prior experience working in OT environments across a variety of verticals to include Energy, Oil and Gas, Chemical, Pharmaceutical and/or related industries. Specialty in one or more of the following OT domains:  Network Architecture, Inventory Gathering, Situational Review, Endpoint Protection, Policy & Governance, Standards, Education & Awareness Experience working in a consultant capacity or within an organisations OT environment to establish roadmaps to improve their current security posture and developing the functional/operational processes and procedures to support their mission. Prior experience leading an assessment or evaluation of an OT environment to include execution of the assessment, analysis of results, and formulation of a final report for dissemination to key stakeholders. Prior experience evaluating and assessing large organisations from the standpoint of OT. Cyber security certifications such as CISSP, CEH, GCIA, GCIH, GCFE etc. Knowledge of industry best practices and standards to include but not limited to the following; IEC 62443, NERC CIP, NESA, OG86. Any exposure to NID D would be advantageous. Why we’re different At Capgemini, we help organisations across the world become more agile, more competitive and more successful. Smart, tailored, often-groundbreaking technical solutions to complex problems are the norm. But so, too, is a culture that’s as collaborative as it is forward thinking. Working closely with each other, and with our clients, we get under the skin of businesses and to the heart of their goals. You will too.  Capgemini positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, gender identity, religion or belief, marital status, or pregnancy and maternity. We are committed to hiring, developing and retaining the best people to deliver innovative, world-class solutions for our clients.  We foster an inclusive culture that enables everyone to achieve their full potential and enjoy a fulfilling career with us. Our comprehensive flexible benefits package and lifestyle policies enable our employees to balance their individual, family and work-life needs.

At Vision Express we’re passionate about what we do, and customer satisfaction is at the top of our agenda. From our stores to our support centre....everyone has a key part to play.  Based in Ruddington, Nottingham we're looking for a talented individual to work within our central operations team as an Operations Business Analyst. You'll be partnering with key stakeholders within the business to offer insight and analysis on key business projects and strategies.  Key responsibilities of the role include: Data modelling and providing insight to our senior management team on store performance and key KPIs Tracking any risks and opportunities, presenting key themes to key stakeholders in the business Working closely with stakeholders across the business on complex projects, assisting from an analytical angle from start to end ensuring that it is completed within a timely manner. Assisting in the planning and scoping of initiatives by collating the data to ensure our management team have all the information needed to make informed decisions.  Maintaining an awareness of how the business operation works, assisting stakeholders in exploring technology possibilities to effectively execute their roles. Building relationships with stakeholders throughout the business, partnering with our management team to become an advisor for continuous improvement   Job Requirements   To be successful in this role you’ll ideally need: Previous experience in a similar role within a fast-paced environment To be professional, adaptable and organised team player To be assertive and credible and will have the ability to influence, guide and support key stakeholders Excellent verbal and written communication skills Previous data modelling skills Have a business mindset and results orientated To be proactive and always striving for continuous improvement Alternatively, this role will be suitable for a graduate who is keen to progress their career. This role will require regular travel across the UK and therefore a full, clean driving licence is essential. You'll be joining a team that always goes the extra mile so if you think this sounds like you then we'd love to hear from you. There's no better place to express your potential.

Responsible for providing support for ongoing remediation and refresh of existing clients. As a specialist member of the KYC (Know Your Customer) team responsible for supporting Standard Risk Refresh activity by carrying out partial refreshes in accordance with the Bank's guidelines and in compliance with UK & global financial regulations.  What you’ll be doing? Provide support to the team including special jobs, gathering and dissemination of data, and support to Team Leaders Lliaise with front office colleagues to ensure no date conflicts exist between source system and completed Tax operations forms Manually carry out Business Analysis Reviews (BAR) on completed cases ensuring all the required actions have been carried out before the case is forwarded to QC Use a high level of attention to detail to complete tasks ‘right first time, every time’, ensuring the KYC Team’s ‘right first time’ targets are met for all tasks Support team leaders in completion of a range of administrative tasks as required Contribute to a supportive and proactive working culture by sharing knowledge and expertise with other team members and providing training to colleagues when necessary Ensure the Team meets all target SLA’s, and providing a quick and efficient service  What we’re looking for: Proven experience in a target driven role Good stakeholder management and communication skills The ability to work as part of a team  Skills that will help you in the role: Good knowledge and understanding of the legislation that affects Barclays and our Clients (including the Data Protection Act, Companies Act, Insolvency Act, Financial Services Act, Money Laundering and confidentiality regulations) could this be moved to the desirable section? Knowledge of the roles and business activities carried out by other teams in the Corporate Bank - as well as across Barclays’ other business functions – with an understanding of how these relate to the KYC Team’s role and business activities. Prior experience with using the Corporate Bank’s computer systems (such as Customer Fullserve) would also be valuable. Where will you be working? Barclays, Glasgow: Where the best meet to build careers full of scope, variety and reward. Creating the solutions that meet today’s demands, answer tomorrow’s questions, and redefines the future of finance. Visit home.barclays/who-we-are/ for more details.  Our Values Everything we do is shaped by the five values of Respect, Integrity, Service, Excellence and Stewardship. Our values inform the foundations of our relationships with customers and clients, but they also shape how we measure and reward the performance of our colleagues. Simply put, success is not just about what you achieve, but about how you achieve it.  Our Diversity We aim to foster a culture where individuals of all backgrounds feel confident in bringing their whole selves to work, feel included and their talents are nurtured, empowering them to contribute fully to our vision and goals. Our Benefits Our customers are unique. The same goes for our colleagues. That's why at Barclays we offer a range of benefits, allowing every colleague to choose the best options for their personal circumstances. These include a competitive salary and pension, health care and all the tools, technology and support to help you become the very best you can be. We are proud of our dynamic working options for colleagues. If you have a need for flexibility then please discuss this with us.

RTI Health Solutions provides consultancy and research services to pharmaceutical and other healthcare industry clients. We are looking for a dynamic and talented candidate to launch their career within our European-based Health Economics team. As a Research Health Economist, you will work within an experienced team in a friendly and collaborative environment.  As part of our team, you will perform leading-edge research to evaluate the clinical, humanistic, and/or economic value of new medicines and other healthcare products.   Our research is used by Health Technology Assessment authorities worldwide to inform their decisions about the availability, pricing, and reimbursement of new healthcare interventions. We offer the opportunity to build a rich, rewarding career, tackle new challenges, publish and present your research, and enhance the depth and diversity of your skills. This position is an office-based position that is located in our Manchester, UK office.   Responsibilities: Coordinate and support health technology assessments (HTAs) and submissions to reimbursement and regulatory agencies such as NICE, SMC, G-BA (AMNOG), TLV, and HAS Conduct clinical and economic systematic and targeted literature reviews to HTA standards Conduct health economics and outcomes research to support cost-effectiveness, budget impact, and cost of illness, and support multi-country adaptation of these analyses Write reports and proposals Implement and deliver high-quality scientific projects to agreed timelines and budgets under direction of senior staff Communicate effectively (via email, telephone, and in-person) with clients and team members regarding projects and proposals Begin to build scientific stature through publication in peer-reviewed journals and conference symposia Develop conference presentations/posters and manuscripts  Qualifications: Master’s degree and a minimum of 1 year of experience in HTA organizations, pharmaceutical industry, contract research, consulting to the pharmaceutical industry, or related area in Pharmaceutical Policy, Pharmacy Administration, Economics, Health Economics, Biostatistics, or a related field.  Familiarity of HTA guidances such as NICE, SMC, G-BA (AMNOG), TLV, and HAS Experience related to creating reimbursement submissions for pharmaceuticals and/or medical devices for multiple countries Coursework or experience in conducting searches in electronic databases and knowledge of systematic review process Experience/familiarity with primary data collection studies; analysis of health care claims, registries, or survey data from the outcomes perspective; cost-effectiveness and budget impact modeling using decision modeling approaches such a Markov and simulation; and cost-of-illness studies would be an advantage Demonstrated skills for reading, writing, and synthesizing scientific research material including evaluation and summarizing of research findings, data extraction, and critical appraisal of the literature High level of attention to detail, organizational skills and accuracy; ability to multi-task and prioritize work and be flexible depending on client deadlines Enthusiasm, commitment and ability, to produce consistently high-quality work within tight deadlines Proficiency in Microsoft Office, specifically MS Word and MS Excel Ability to work well independently and as part of a team Demonstrated interpersonal and communication skills (both written and oral) RTI Health Solutions (RTI-HS) is a business unit of RTI International. We provide scientifically rigorous research and consulting services to pharmaceutical, biotech and medical device companies. Our various practice areas include: Health Economics, Patient Centered Outcomes Assessment, Pharmacoepidemiology, Market Access and Outcomes Strategy, Biostatistics, Clinical Services, and Health Preference Assessment.