1+ months

Quality Control Analyst I- 2nd Shift

Elizabeth, NJ 07201
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.  

 

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

This position performs analyses, inspection, and testing of products, raw materials, in-process materials, release test samples, stability samples, or packaging materials.  Performs qualitative and quantitative assays on samples, to ensure quality standards and compliance with company standards, customer and governmental regulatory requirements, and product specifications for the chemical or physical properties.  Uses approved Test Methods, Protocols, Procedures (SOPs) and Corporate Policies while maintaining adherence to current industry standards.  Employs variety of analytical techniques that vary from standard analytical equipment to highly modern and automated instrumentation, aides in maintenance and certification of test instruments and apparatus to ensure compliance. May be involved or responsible for performing Laboratory Investigations, Change Controls, audit/review of laboratory data, implementing CAPA, Planning and scheduling laboratory activities, and coordinating process improvements.

 

**This is a 2nd Shift position**

 

Essential Duties / Functions

  • Follow established laboratory safety procedures.
  • Analyze samples using appropriate instrumentation (depending on training, some or all of the following would apply HPLC, GC, UV, IR, KF, pH, etc.) while following current Methods & Procedures (SOPs).
  • Process and report HPLC instrumental analysis using Empower data processing software.
  • Process and report other instrumental analysis 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 new and current employees.

Education Required:

  • BS/BA                                                                                

 

Experience Required:

  • 1 year in a pharmaceutical laboratory environment.

 

Specialized or Technical Knowledge, Licenses, Certifications

  • Must possess knowledge regarding various tests and wet chemistry techniques that pertain to Raw Material 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.)
  • Knowledge of cGMPs.
  • Knowledge of compendia procedures where applicable (i.e., USP, NF, BP, etc.).
  • Possess good written and oral communication skills.
  • Proficiency with  Empower software and Microsoft Office Word and Excel.
  • Possess strong mathematical skills fractions, percentages, ratios and algebraic expressions.
  • Possess good problem solving skills 

 

Physical Demand Requirement

  • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.  Approximately 60% standing or walking.

Categories

Posted: 2019-10-14 Expires: 2019-11-26

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 I- 2nd Shift

Teva Pharmaceuticals
Elizabeth, NJ 07201

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