Teva Jobs

Analytical Development Chemist III

Date: Jun 25, 2024

Location:

Toronto, Canada, Ontario, M1B2K9

Company: Teva Pharmaceuticals

Job Id: 56681

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

In this position, the Analytical Development Chemist III must develop, revise and validate analytical methods (for commercial and stability samples) of limited complexity using common analytical laboratory instruments, such as HPLC, GC, Dissolution and titrators, in accordance with the appropriate SOP’s under the supervision of the senior chemist. The incumbent will also conduct method transfer as well as testing to support Technical Service Department. The incumbent will also prepare various types of summary reports (e.g. method validation report, method transfer report) upon completion of the study.

How you’ll spend your day

• Plans and performs analytical method development, validation and method transfer for various analytical techniques for physical and chemical analysis of pharmaceutical materials.

• Develops and validates, in compliance with all current SOP’s and regulatory requirements, analytical methods of limited complexity with assistance from the senior chemist.

• Prepares method validation reports summarizing analytical data in concise write-ups of high quality in a timely manner.

• Plans and fully co-ordinates most aspects of work in a logical fashion and performs in an accurate and timely manner that is cost effective.

• Displays good problem solving skills and shows innovation on an on-going basis.

• Operates and troubleshoots analytical laboratory instruments such as HPLC, UPLC, GC, Malvern Particle Size Analyzer, UV, FTIR, ICP-MS and Dissolution Apparatus.

• Displays very good written and verbal communication skills.

• Contributes to the participation of the QC support group in the Quality Control Laboratory.

• Ensures the efficient timely completion of work in accordance with the established priorities.

• Actively participates in meetings with Supervisor and peers to ensure collaboration and information is collected to make informed decisions in order to resolve issues.

• Collaborates with other QC Lab groups to help capture synergies, organize, and prioritize requirements meet established goals.

• Participates in the implementation of processes in the Quality Control Laboratory to expedite analytical testing, improve customer service, reduce operational costs and improve laboratory safety.

• Effectively communicates, exhibits the company values, maintains priorities and monitors training to ensure a high standard of performance.

• Adheres to, safe operational practices to prevent accidents and avoid danger to others in the workplace.

• Perform all test folloowing GMP regulations and health and safty princilples.

• Supporting Tech Services activities.

• Performs and if needed recommends analytical testing including dissolution, disintegration, assay, impurities and CU/BU etc., to support any formulation and process changes as well as technology transfer projects.

• Supports evaluations of the analytical data to identify and resolve product chemistry, uniformity and drug dissolution related issues.

• Provides feedback and suggestions to Tech Services.

• Performs other related duties as required.

Your experience and qualifications

Required: University Degree or College Diploma in Chemistry or related science

2+ years of experience in the related field

Solid knowledge of:

• Method validation fundamentals and requirements

• Analytical laboratory equipment common in QC Lab environment (HPLC, UPLC, GC, Dissolution, Particle Size Analyzer, UV, FTIR, and ICP-MS etc.).

• Technical requirements as per compendia (USP/NF,BP/EP), in- house methods and general QC laboratory procedures

• ICH guidelines, GMP/cGMP regulations as they apply to the laboratories.

Demonstrates good written and verbal communication skills in order to:

• Interpret analytical data and discuss the issues/problems with the manager and senior chemists if required.

• Write in a lucid format, Technical evaluation reports, validation/method transfer reports and other relevant QC documents

Knowledge of, and experience in a Quality Control Laboratory and working knowledge of GMP/cGMP as they pertain to QC laboratory unit.

Analytical methods and techniques common to QC Lab

Computer skills with proficiency in Microsoft Office and Labware LIMS, navigating online compendia publications

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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)

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.

EOE including disability/veteran