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Job Details

Quality Control Analyst II

East Mansfield, MA, United States

Posted on
Jun 26, 2020

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Jun 26, 2020
Haarlem, NL, 2031
Our Company

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!
Our Department

The Quality Control Analytical Laboratory is responsible for all analytical testing to support the production Cytotoxic and Inhalation drug products. The laboratory executes a wide variety of analytical test package to test APIs, excipients, packaging materials and drug products for release and stability purposes. Also transfer, validation and verification of analytical methods for testing of new drug products are performed in the laboratory. As a result of the increase of products to be tested the Quality Control Analytical Laboratory teams Parenteral IPC&Release, Raw Materials &ICP and Stability &Investigations are searching for a Quality Control Analyst to join us.
Your Role

Routine Testing of the raw materials, primary and printed packaging materials & finished products, stability samples and in-process control samples according to SOP and as per the committed time lines.
Handle quality management system like Deviations, Out of specification results (Phase 1 investigation), Out of trend results in stability as well as in released products,
Writing, review and approval or reject of test results
Act as team lead in absence of Group leader (applicable to function in 24/7 shift teams)
Maintain adherence to corporate policies and appropriate regulations through actions and decisions
Active participation in advanced problem solving, root cause analysis, troubleshooting, interpretation/consultation, verification of quality and test results discussions
First-line Troubleshooting of laboratory equipment
Active participation in changes or act as change owner as part of continuous improvement.
Your Profile

Bachelor degree in analytical chemistry/pharmacy or equivalent experience
Knowledge and familiarity with the use of Pharmacopoeia methods
A strong analytical oriented mindset.
Experience with working in a pharmaceutical environment
Experience with development/validation or verification of analytical methods for complex drug products like liposomal or protein coated drugs
Experience with analytical techniques like, UPLC/HPLC, TOC, PSD, etc.
Good knowledge of Pharmaceutical quality systems and production processes
Experience & exposure to work in regulatory environment as well as Regulatory Audit like EU cGMP inspection , US-FDA, ANVlSA
Team player
Strong can-do mentality
Results oriented
Competence to act as team lead in absence of a Group leader

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’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.
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