Fulltime- Camarillo- 2nd Shift

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BACHELORS DEGREE IN A TECHNICAL OR SCIENTIFIC SKILL OR A HIGH SCHOOL DIPLOMA WITH 0-3 YEARS OF EXPERIENCE

·         UNDERSTANDING OF GLOBAL PHARMACEUTICAL PRODUCT REGULATIONS WITH EXPERIENCE WITH ISO 9001 AND OR 13485 2003 AND 21 CFR PARTS 210 AND 211 WITH PART 820.

·         DEMONSTRATE THE ABILITY TO PERFORM GMP OPERATIONS FOLLOWING DETAILED SOPS, MAINTAINING TRAINING DOCUMENTS AND OR GOOD DOCUMENTATION PRACTICES.

·         0-3 YEAR TECHNICAL DOCUMENTATION FOR QUALITY ACTIVITIES. SPECIFIC TO MANUFACTURING.

·         SOLID ORGANIZATIONAL SKILLS

·         ABILITY TO COMMUNICATE EFFECTIVELY, VERBALLY AND IN WRITING WITH DETAILED REPORT WRITING AND TECHNICAL WRITING SKILLS.

·         THE ABILITY TO INTERDEPARTMENTALLY WORK WITH VENDORS AND CONTRACTORS.

·         TEAM ENVIRONMENT.

·         RESPONSIBLE FOR ALL ACTIVITIES INVOLVING QUALITY ASSURANCE AND COMPLIANCE WITH APPLICABLE REGULATORY REQUIREMENTS.

·         INITIATE, INVESTIGATE AND COMPLETE NONCONFORMANCE REPORTS

·         SUPPORTS THE GENERATION OF PRODUCT CERTIFICATE OF COMPLIANCE

·         RESPONSIBLE FOR THE LABEL CONTROL AND PRINTING

·         PROVIDE HELP AND SUPPORT FOR ALL ASPECTS OF TESTING RELATED TO MANUFACTURING

·         FIRST ARTICLE INSPECTIONS

·         IN PROCESS RELEASE INSPECTION

·         FINAL QC RELEASE OF FINISHED GOODS

·         DOCUMENT REVIEW

·         ENSURES THAT ALL INSPECTIONS AND PROCEDURES ARE PROPERLY COMPLETED AND DOCUMENTED.

·         ENSURES DOCUMENTS ARE ENTERED IN THE QUALITY DATABASES, SCANNING, INDEXING AND FILING WHILE ARCHIVING OLD DOCUMENTS.

APPLY:

Please apply 2011 Auto Center Drive, Oxnard, CA 93036 Suite 116

Bring 2 Forms of ID and updated Resume

805-485-4606 with any questions

 

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