Job Description

Who are we?

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Analytical Chemistry Scientist (On-site)

The Analytical Chemistry Scientist serves as a technical expert in analytical chemistry within the R&D laboratory. This role is responsible for the technical execution of assigned tests, as well as the interpretation, analysis, documentation, and reporting of results. The ideal candidate will have extensive knowledge and experience in chemistry and analytical techniques, and will contribute to method development, optimization, validation, and transfer. Effective communication with cross-functional teams is essential.

Key responsibilities

General

•    Prepare and review written procedures including SOPs, and protocol test procedures for laboratory analysis.
•    Maintain a clean and safe work enviroment, including work area, instrumentation and testing materials. 
•    Ensure sample and data traceability throughout all testing processes.
•    Accurately perform calculations and statistical analyses, ensuring they reflect the raw data.
•    Ensure test controls and monitors are accurately recorded and reviewed.
•    Continually work to optimize the results of the instruments with new parameters or instrument setups.
•    Evaluate and implement new analytical approaches, including software tools, to further strengthen the group’s technological capabilities.

Quality responsibilities

•    Adhere to cGMP and GLP regulations. 
•    Follow all company policies and procedures.
•    Ensure compliance with current regulations and complete required training on time.
•    Properly record, interpret, and manage analytical data.
•    Review data quality and recommend improvements to methods or procedures as needed.
•    Review test results and peer work for accuracy and compliance.

Project Management

•    Meet project deadlines.
•    Collaborate with other departments to improve workflow and ensure successful project completion.
•    Problem-solving and troubleshooting skills.
•    Demonstrated planning and organizational skills in order to complete R&D activities.
•    Design, implement, and manage studies related to drug product characterization.

Professionalism

•    Work independently and as part of a team to meet organization and projects objectives.
•    Demonstrate adaptability, flexibility, and forward-thinking in technical matters.
•    Engage in continuous learning, review scientific literature, and attend meetings to stay current with new developments.
•    Proficient in Microsoft Office applications (Word, Excel, Outlook) and business related application packages, such as Empower, Chromeleon or similar software, with the ability to learn new applications as needed.
•    Exceptional oral and written communication skills to all levels of the organization.

Education

M.S. / B.S. degree in Chemistry, Biochemistry, Pharmacy or related scientific field (Chemistry strongly preferred) with 0 - 4 years of experience in the pharmaceutical industry.
Ph.D. in analytical chemistry, biochemistry, or related field with 1-2 years experience.
Strong analytical knowledge across multiple techniques, including at least HPLC, UV, GC, particle size analysis, Karl Fischer titration, and TLC.

Function

Research & Development

Sub Function

Drug Development and Preclinical Studies

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

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