Teva Analytical Researcher 

Romania 

14238233

Analytical Chemistry Scientist provides scientific knowledge and will be considered the technical expert in the assigned area. We are looking for a candidate with extensive scientific knowledge and experience in the area of Chemistry and analytical techniques, that will take the overall responsibility for the technical conduct of all assigned tests as well as for the interpretation, analysis, documentation, and reporting of results. Job requirements include efficient sample analysis, data interpretation, developing new analytical methods, optimizing current analytical methods, validating and transferring the analytical methods and effectively communicating results to cross functional teams.

M.S. / B.S. degree in Chemistry, Biochemistry, Pharmacy or related scientific field with 2 - 4 years experience in Pharma industries.
Ph.D. degree in analytical chemistry, biochemistry, or related scientific field with 1-2 years experience.
Analytical knowledge across many techniques is highly desirable including at least HPLC, UV, GC, particle size analyzer, KF, TLC.

General
• Prepare and review written procedures including SOPs, and other protocol test procedures and instructions that will be followed during analysis.
• Maintain a clean and safe work enviroment including work area, instrumentationa and testing materials.
• Ensure sample and data traceability are maintained throughout testing.
• Ensure calculations and statistics accurately 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
• Know and follow cGMP, GLP regulations. Continues to develop a cGMP awareness by obtaining a more comprehensive understanding of cGMP’s, GLP’s.
• Know and follow company policies and procedures.
• Ensure compliance on current regulations.
• Complete required training on time.
• Proper recording, interpretation, and management of analytical data.
• Review general data quality to determine where changes to methods or procedures could improve quality.
• Review test result.
• Review peer's work.

Project Management
• Meet turn around deadlines.
• Manage workflow improvements working with other sections and functions within the company to ensure successful completion and implementation.
• Problem-solving and troubleshooting skills.
• Demonstrated planning and organizational skills in order to complete R&D activities.
• Capable of designing, implementing and managing studies related to the characterization of drug product.
Professionalism
• Ability to work independently and as part of a team to meet organization and projects objectives.
• Able to be technically adapt, flexible and forward thinking.
• Continually learn and train, review scientific literature, and attend meetings to keep current with new technical and scientific information
• Proficient in the use Microsoft Office applications (Word, Excel, Outlook) and business related application packages, such as Empower, Chromeleon or similar software, plus the ability to learn company used applications.
• Exceptional oral and written communication skills geared to all levels of the organization

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