QA Specialist

Strong working knowledge of FDA QSRs as well as ISO 9001 and ISO 13485 required. Responsibilities include: equipment validation; performing internal quality audits; support maintenance of CAPA and NCMR system. Dako provides excellent benefits and opportunities for career growth EOE. No phone calls please. Dako is an international, biomedical products company that manufactures and markets immunological reagents and instrumentation for use in clinical and research laboratories. Dako provides excellent benefits & opportunities for career growth. EOE. No phone calls or third parties please. Send resume with salary history to: Dako Human Resources 6392 Via Real Carpinteria, CA 93013 Fax: 805 684-5935 [Click here for email]
REQUIREMENTS
Strong working knowledge of FDA QSRs as well as ISO 9001 and ISO 13485 required. Position requires a BA/BS degree in Chemistry, Biochemistry, Microbiology or equivalent with 3+ years of QA experience in cGMP/QSR manufacturing environment. Medical device development and manufacturing experience preferred.