Analytical Researcher

Who we are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. The opportunity

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.

Education 

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.

Essential Duties

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

 

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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

---