Teva Analytical Chemistry Scientist On-site 

Romania, Bucharest 

363652752

• 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.

• 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.

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.

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