Posted in General Business 30+ days ago.
Type: Full-Time
Rhodes Pharmaceuticals L.P. has developed and distributed quality pharmaceutical products nationwide since 2008. With our R&D capabilities, industry partnerships, broad customer base, and strong relationships with suppliers, we offer reliable supply of high-quality products at competitive prices. Rhodes is a wholly-owned subsidiary of Purdue Pharma L.P.
We are driven by our purpose: Compassion for patients and excellence for science inspire our pursuit of new medicines.
We are building an exciting path forward, and we are committed to recruiting a dedicated team of professionals who advance our expertise through a commitment to our Values: Integrity and Courage, underpinned by Innovation, and always in Collaboration with each other.
At Purdue Pharma and our subsidiaries, you have a unique career opportunity to work differently, uncover and seize new opportunities, and take a hands-on, ownership approach to your work. We go beyond traditional roles and find creative ways to extend our skills and interests, challenging ourselves to contribute in different, meaningful ways. We strive to create an environment where you can bring your best to work each day. We welcome the opportunity to have you on our team!
Job Summary
Provide strategic direction and input to all Quality activities at the Coventry site. Assure succession for key Quality roles for Rhodes Pharmaceuticals and support business activities and projects. Ensure quality activities at external contract development organizations and GMP commercial suppliers or contract manufacturers and the materials/finished product supplied by these firms meet all appropriate regulations and Purdue company and subsidiary requirements.Quality interfaces between the companies are data driven and serve to further improve the quality of the supplied material while maintaining a reliable supply chain.
Responsible for establishing the Quality Systems and procedures for the GMP development life cycle for third party development, clinical supply, and commercial manufacturing, packaging, testing and distribution of drug products.
Provide QA oversight of product development, submission batch manufacture, regulatory dossier development, validation activities and technology transfer, as needed ensuring compliance with current regulatory thinking and industry best practices, including risk-based scientific rationales for value-added validation.
Primary Responsibilities
Education and Experience Requirements
BS required for external applicants and 15+ years minimum experience in a pharmaceutical technical operations/QA leadership role, or equivalent level of experience in pharmaceutical or related industries; or graduate degree (MS preferred) with 10 years minimum experience or PhD with 8 years minimum experience.Minimum of 3 years of experience in providing QA oversight of suppliers/contract manufacturers.
Necessary Knowledge, Skills, and Abilities
Supervisory Responsibilities (if Applicable)
Manages a team of Quality Assurance professionals responsible for providing technical oversight of suppliers and contractor developers and manufacturers at multiple US and international locations.
Additional Information
Purdue Pharma L.P.& its Subsidiaries are an Equal Opportunity (EEO) and Affirmative Action Employer encouraging diversity in the workplace.Qualified applicants will receive consideration for employment without regard to their race, national origin, religion, age, sex, sexual orientation, marital status, gender identity, genetic information, disability, military, protected veteran status, or any other characteristic protected by local, state, or federal law. Protected veterans and qualified individuals with a disability may request a reasonable accommodation by emailing: careers@pharma.com .
For more information about your rights under Equal Employment Opportunity, visit:
EEOC Poster
EEOC GINA Supplement
EEO is the Law Poster Supplement
OFCCP Pay Transparency
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