What are the responsibilities and job description for the QA Specialist position at Technical Source?
Technical Source is currently in search of a Quality Assurance Specialist for our pharmaceutical client located here in the Greenville, NC area. The qualified candidate will have experience reviewing and approving GMP documentation, SOPs, and protocols.
Responsibilities of the Quality Assurance Specialist include:
- Provide working knowledge and oversight of QA principles related to validation activities to ensure compliance of pharmaceutical manufacturing equipment
- Review and approve validation protocols and documentation for pharmaceutical manufacturing equipment
- Maintain knowledge of current local and international GMP regulatory requirements.
Qualifications of the Quality Assurance Specialist include:
- 3 years’ experience of providing QA oversight in a pharmaceutical manufacturing environment
- Bachelor’s or Associates degree in related field preferred
Compensation for the Quality Assurance Specialist includes:
- $40 – $55 per hour based on experience
- Full benefits, medical, dental, and vision
- No Corp to Corp or Visa sponsorships at this time
Key Words:
Validation, IQ, OQ, PQ, Engineering, automation, pharma, commissioning, qualification, Quality control, quality assurance, technical documentation, document control, workflow, files, document management, auditing, engineering, pharma, pharmaceutical, contract to hire, contract, permanent, full time, benefits, 401K, direct hire, cell culture, gene therapy, temperature mapping, lab equipment, KAYE, Fill/finish, sterile, upstream, downstream, process, QA, Quality Assurance, SOP, Protocols, regulatory, compliance, GMP
Job Type: Full-time
Pay: $40.00 - $55.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Vision insurance
Schedule:
- 8 hour shift
Work Location: Multiple Locations
