Job Description

Quality Control Technician III

Date: Apr 7, 2023



Location: Sunrise, Florida, United States, 00000



Company: Teva Pharmaceuticals



Job Id: 47086

Who are we?

If you\xe2\x80\x99re like people at Teva, you dare to be different. We\xe2\x80\x99re making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.

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.

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.

POSITION SUMMARY

This position is responsible for maintaining the laboratory areas in conformance with regulations and standards. This includes performing all laboratory cleaning, environmental monitoring and utilities testing.
ESSENTIAL AREAS OF RESPONSIBILITY
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\xe2\x80\x99s), Standard Operating Procedures (SOP\xe2\x80\x99s) and Batch Record instructions.
• Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
• Responsible for performing sampling of water system points of use (POU) following guidelines and maps. Perform TOC and conductivity tests on the water samples.
• Sample Raw Materials following gowning requirements and written instruction from sampling plan.
• Perform Environmental Monitoring sampling by following sampling points and locations.
• Support Environmental Monitoring during liquid compounding and aseptic filling.
• Clean QC Laboratory Glassware
• Review chart recorder and replace them accordingly.
• Perform general housekeeping for the QC Lab.
• Support the QC Lab with Biohazard waste disposal following written instructions.
• Maintain the Laboratory material and reagents inventory.
• Perform routine basic work (i.e. Karl Fisher, LOD, etc.) as well as Solution/Media Preparation.
• Ability to train and qualify in aseptic gowning techniques, as well as, perform all required tasks in an aseptic environment while wearing sterile gowns.
• Maintains accurate records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization).
• 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 a high school diploma and 4+ years of relevant progressive experience in the pharmaceutical industry; or an Associate of Science degree or equivalent with a minimum of 2+ years of relevant progressive experience in the pharmaceutical industry.

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\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.