1+ months

Quality Control Analyst III

Elizabeth, NJ 07201
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Company Info

Teva is a global pharmaceutical leader and the worlds 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 worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve 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!

 

We offer a competitive benefits package including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance.

 

This position is located in 200 Elmora Ave, Elizabeth, NJ 07202

 

For more on Teva, check us out at www.tevapharm.com or www.tevausa.com.

Job Description

Position Summary: 

This position performs analyses, inspection, and testing of products, raw materials, in-process materials, release test samples, stability samples, and/or packaging materials.  Performs qualitative and quantitative analyses on samples to ensure quality standards and compliance with company standards, customer and governmental regulatory requirements, and product specifications for chemical or physical properties.  Uses approved Test Methods, Protocols, Procedures (SOPs) and Corporate Policies while maintaining adherence to current industry standards.  Employs a variety of analytical techniques, which vary from standard analytical equipment to highly modern and automated instrumentation. Aids in the maintenance and certification of test instruments and apparatus to ensure compliance. May be involved or responsible for performing Laboratory Investigations, Change Controls, auditing/reviewing of laboratory data, implementing CAPAs, planning and scheduling of laboratory activities, and coordinating process improvements.  May be assigned project work such as analytical method transfer, which requires preparation of protocols and reports or other documentation as required by the assignment.

 

Key Responsibilities:

  • Follow established laboratory safety procedures.
  • Analyze samples using appropriate instrumentation (depending on training, some or all of the following would apply HPLC/UPLC, GC, UV, IR, KF, pH, etc.) while following current Methods and Procedures (SOPs).
  • Process and report analytical data using Empower data processing software.
  • Process and report other instrumental analyses using the instrument-specific data processing software.
  • Document all activities in a legible manner following established formats and procedures.
  • Identify and troubleshoot problems with instrumentation and analytical preparations.
  • Initiate and conduct laboratory investigations.
  • Review and approve analytical data.
  • Participate in process improvement projects.
  • Train and/or mentor new and current employees.
  • Capable of reviewing and revising procedures as needed, including applicable change control documentation.
  • Prepare clear and accurate reports, including laboratory investigations, as assigned.
  • Participate in method transfer, method development, method evaluation, method verification or other investigative testing/ project work, including protocol and report development and documentation.
  • Interact with vendors and/or contract laboratories as required to support assigned responsibilities.

Qualifications

Education:

  • BS/BA in Chemistry, or BS in a Related Science

 

Experience:

  • Minimum 7 years in a pharmaceutical laboratory environment

 

Specialized or Technical Knowledge required:

  • Strong knowledge of compendia procedures and general chapters, where applicable (i.e., USP, NF, BP, etc.).
  • Reviewing the compendia and associated websites to identify changes or pending changes with the potential to impact site procedures (methods, SOPs) and specifications
  • Organizing and chairing Compendial Review Board (CRB) meetings.
  • Working with appropriate departments to identify subject matter experts (SMEs) to assess/implement the changes.
  • Initiate a Trackwise Preventive Action to the SMEs.
  • Tracking the progress to ensure compliance with changes.
  • Must possess strong technical knowledge regarding various tests and wet chemistry that pertain to Raw Materials and/or Finished Product analyses (depending on assigned product line, some or all of the following would apply Viscosity, Thin Layer Chromatography, various forms of Limit Tests, etc.).
  • Strong instrumental analysis skills including HPLC/UPLC/ GC, UV, etc.
  • Knowledge of cGMPs.

Function

Quality

Sub Function

Manufacturing Quality Control

Reports To

Associate Director, Quality Control

Tevas 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.

Posted: 2019-06-05 Expires: 2019-09-05

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Quality Control Analyst III

Teva Pharmaceuticals
Elizabeth, NJ 07201

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