Job title: Senior Quality Control Associate (Potency / In-vitro Assay Systems)
Company: Teva Pharmaceuticals
Expected salary:
Location: West Chester, PA
Senior Quality Control Associate (Potency / In-vitro Assay Systems) Job Details:
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.
The opportunity
As a Senior Quality Control Associate you will have prior experience in GMP bioassay testing and assay validation, and an understanding of regulated work and compliance. Experience with a variety of biological in-vitro assay systems is preferred. Meticulous attention to detail in following procedures (e.g. SOPs), preparing written documentation, data analysis and execution of experiments is required. Maintaining local, regional and global regulatory compliance (ICH, FDA, GMP, OSHA, etc.) are integral responsibilities of this position.
*** THIS POSITION IS 100% ON-SITE IN WEST CHESTER, PA, US ***
RELOCATION ASSISTANCE AND WORK VISA SPONSORSHIP IS NOT AVAILABLE
How you’ll spend your day
- Perform release and stability testing, record data per GxP requirements and provide peer review of documentation.
- Participate in method transfer and validation activities.
- Develop methods and perform method optimization.
- Participate in the writing and review of SOPs, work instructions, protocols and reports
Your experience and qualifications
Required:
- Bachelor’s degree in Biology or related field of study with a minimum of 5 years of experience in laboratory setting within the pharmaceutical industry
OR
- Master’s degree in Biology or related field of study with a minimum of 3 years of experience in laboratory setting within the pharmaceutical industry.
Preferred:
- Experience with a variety of biological in-vitro assay systems.
Enjoy a more rewarding choice
Make a difference with Teva Pharmaceuticals
Reports To
Senior Director, Quality Control, Biologics CMC, West Chester – US
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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.
Important notice to Employment Agencies – Please Read Carefully
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
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