Location: Remote
Job ID: 794
Number of Openings: 0
Company Overview:
Crinetics Pharmaceuticals, headquartered in San Diego, California, is dedicated to developing transformative therapies for endocrine diseases and related tumors. Founded by a team of visionary scientists, we are committed to rigorous innovation to enhance patient outcomes. As a growing company, we offer a dynamic, inclusive, and dog-friendly work environment. Join us in shaping the future of endocrine care and make a meaningful impact on patients' lives.
Position Summary:
The Senior Specialist, GMP Quality Assurance is pivotal in ensuring compliance with Good Manufacturing Practices (GMP) across our manufacturing and support operations. This role involves performing batch record reviews, analyzing analytical and microbiological testing, and supporting internal and external GMP audits. The ideal candidate will be a detail-oriented professional with extensive experience in GMP environments and a solid understanding of drug substance and drug product quality assurance.
Key Responsibilities:
Education and Experience:
Required:
Preferred:
Physical Demands and Work Environment:
Compensation and Benefits:
Equal Opportunity Employer:
Crinetics is committed to providing equal employment opportunities without discrimination. We adhere to all applicable local, state, and federal laws regarding equal employment practices.
Vaccination Requirement:
Crinetics requires all employees and contractors to be fully vaccinated against COVID-19 as a condition of employment. Those unable to be vaccinated due to a medical condition or sincerely held religious belief may request a reasonable accommodation.
Application:
If you are a qualified candidate who is passionate about quality assurance and GMP compliance, we encourage you to apply. For more details about our company and this opportunity, visit our website.
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