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Quality Control Technician II

Date: Aug 4, 2022

Location: Davie, Florida, US, 00000

Company: Teva Pharmaceuticals

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!

Job Description

All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.

  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.  
  • Performs sampling and in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP).
  • Conducts routine analysis of raw materials (identification and assay) using Ultra violet/infrared (UV/IR), thin layer chromatography (TLC) and automatic titration.
  • Prepares standard and sample solutions for HPLC and assists in performing HPLC testing.
  • Maintains appropriate documentation of records and laboratory notebooks as required by SOPs and cGLPs.
  • May receive and control laboratory samples; receives laboratory supplies and chemicals; and maintains inventory control.
  • Washes glassware, ensures cleanliness of testing equipment and complies with good housekeeping practices.
  • Performs testing of drug products, prepare and maintain volumetric solutions.
  • Ensures project deadlines and performance standards are established and met.
  • Ensures compliance with all Company policies and procedures, including safety rules and regulations.
  • Collects and test samples for environmental monitoring of the facility.
  • Prepares and maintains test solutions and reagents.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.  
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) instructions.
  • Responsible for performing additional related duties as assigned.

Qualifications

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered. 

Education/Certification/Experience:

  • Requires high school diploma or equivalent with a minimum of 2 year relevant progressive manufacturing laboratory experience in the pharmaceutical industry.

Skills/Knowledge/Abilities:

  • Following verbal and written directions.
  • Communicating clearly and concisely, both orally and in writing.
  • Operating scientific and personal computers.
  • Establishing and maintaining cooperative working relationships with others.
  • Ensuring compliance with all Company policies and procedures, including safety rules and regulations.
  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
  • Personal computer hardware and software applications.
  • Business English usage, spelling, grammar and punctuation.
  • Basic mathematical computations.
  • Basic chemistry laboratory practices and techniques.
  • Current Company policies, practices and procedures, including safety rules and regulations.
  • Must be able to maintain the highest levels of confidentiality, integrity and discretion.

Problem Solving:

  • Works on assignments that are routine to semi-routine in nature where the ability to recognize deviation from accepted practice is required.
  • Exercises judgment within specifically defined practices and policies and selects methods and techniques for obtaining solutions.
  • Normally receives general instruction on routine work and detailed instruction on new assignments.

Function

Quality

Sub Function

Manufacturing Quality Control

Reports To

In process of validation

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’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.

Teva Pharmaceuticals USA requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, however, Teva will consider requests for reasonable accommodations.