Job Description

Analytical Chemist IV

Date: Feb 3, 2023



Location: Toronto, Ontario, Canada, M1B2K9



Company: Teva Pharmaceuticals



Job Id: 44952

Who are we?

Teva is a global pharmaceutical leader and the world\'s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world\'s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we\'ve built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

The Quality Control Laboratory Analytical Investigation Chemist 4 is responsible to work independently under the direction of the 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 along with supervisory support to the QC Laboratory. Tasks include but are not limited to: Assists the Manager with the execution and completion of analytical investigations carried out in QC Laboratory
Performs the analytical investigation process ensuring that the following criteria and steps are adhered to as part of the process.
The following criteria are evaluated with each investigation:

• Appropriate and relevant SOP\xe2\x80\x99s are followed
• Root cause analysis is performed
• Technical/analytical integrity is confirmed
• Historical trending of data (where applicable) is reviewed
• Corrective Action and Preventative Action (CAPA) measures are identified and acted upon
• Completion of investigation by due date

Entries into the appropriate tracking system
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\xe2\x80\x99s 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.
Assists with the supervision of the Quality Control Laboratory as required or in the absence of the Manager.
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.
Effectively communicates, exhibits the company values, maintains priorities and monitors training to ensure a high standard of performance.
Ensures adherence to training and safe operational practices to prevent accidents and avoid danger to staff and others in the workplace.
Perform other related duties as required.

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).
• Functional Knowledge:
• LIMS (Laboratory Information Management System), CDS (Chromatography Data System such as Empower), Trackwise, MSOffice, SAP.
• Company / Industry Related Knowledge:
• Knowledge of, and experience in a Quality Control Laboratory and working knowledge of GMP/cGMP as they pertain to QC laboratory unit.

Function

Quality

Sub Function

Manufacturing Quality Control

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\xe2\x80\x99s 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.