Job Description

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

The Quality Control Laboratory Analytical Investigation Chemist 4 is responsible to work independently under the direction of the Sr. Manager, Quality Control conducting investigations into the integrity of analytical data to identify root causes and determine corrective actions for lab investigations. As an Analytical Investigation Chemist 4, responsibilities also extend to performing analytical testing dealing with complex chemical and physical analyses associated with commercial production and stability samples and providing technical and analytical training when necessary to the QC Laboratory.

How you\'ll spend your day

• Assists the Manager with the execution and completion of analytical investigations carried out in QC Laboratory
• Performs the analytical investigation process ensuring that the required following criteria and steps are adhered to as part of the process.
• Conducts lab investigations using complex trouble-shooting techniques
• Prepare and review analytical reports to ensure that work has been executed according to the procedures specified in specifications and in compliance with all relevant SOPs.
• Perform supplemental validation as required to support CAPA\'s and method improvement and revisions.
• Performs analytical testing of materials associated with commercial production and stability samples.
• Performs complex chemical and physical analyses on commercial production and stability samples in an efficient, safe and compliant (GMP) manner following all applicable Standard Operating Procedures and Analytical Testing Monographs.
• Proficiently employs all analytical techniques and instrumentation within the laboratory.
• Utilizes complex trouble-shooting techniques to resolve analytical problems.
• Produces complete, accurate and clear analytical reports.
• Responsible for the analytical integrity of all work performed.
• Collaborates with supervisor and laboratory group to prioritize projects and utilize resources to ensure deadlines are met in a safe and compliant manner.
• Ensures efficient and timely completion of work in accordance with the established priorities.
• Actively participates in and facilitates meetings with Management and other supervisors to ensure collaboration and information is collected to make informed, critical decisions in order to resolve operational and system issues.
• Assists other QC Lab groups to capture synergies, organize, and prioritize requirements to meet established goals.
• Assists in the implementation of processes in the Quality Control Laboratory to expedite analytical testing, improve customer service, reduce operational costs and improve laboratory safety.
• Perform other related duties as required.

Your experience and qualifications

• University Degree (Ph.D. M.Sc. or B.Sc.) in Analytical Chemistry or a related discipline
• Preferred: Supplementary courses/diploma/certificates such as Quality/Regulatory Affairs, Pharmaceutical Manufacturing, or Risk Assessment considered an asset.
• 3+ Years Laboratory Experience
• Knowledge of technical requirements as per compendia (USP/NF/BP/EP), in-house methods and general QC laboratory procedures.
• Knowledgeable in GMP/cGMP regulations as they apply to laboratories.
• Knowledge of analytical instrumentation (ex. HPLC, UPLC, GC, Dissolution), CDS (Chromatography Data System such as Empower).
• LIMS (Laboratory Information Management System), CDS (Chromatography Data System such as Empower), Trackwise, MSOffice, SAP.
• Knowledge of, and experience in a Quality Control Laboratory and working knowledge of GMP/cGMP as they pertain to QC laboratory unit.

Make a difference with Teva Pharmaceuticals

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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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