Job description
Technical Source is currently in search of a Validation Engineer for our pharmaceutical client located here in the Raleigh-Durham, NC area. The qualified candidate will have experience validating analytical lab equipment used in pharmaceutical drug manufacturing.
Responsibilities of the Validation Engineer include:
- Commission, qualify, and validate analytical lab equipment and computer systems used in pharmaceutical drug development
- Author IQ/OQ/PQ validation protocols including URS, RTM, and FS for computerized analytical lab equipment and systems
- Initiate risk assessment and gap analysis for commissioning of lab instrumentation and lab systems
Qualifications of the Validation Engineer include:
- 3+ years’ experience of equipment validation in a pharmaceutical manufacturing environment
- Strong experience with cGMP documentation review and execution
- Working knowledge of CQV validation process
- Bachelor’s or Associates degree in related field preferred
Compensation for the Validation Engineer includes:
- $80,000 – $120,000 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,
Job Type: Full-time
Pay: $90,000.00 - $120,000.00 per year
Benefits:
- Dental insurance
- Health insurance
- Vision insurance
Schedule:
- 8 hour shift
Ability to commute/relocate:
- Cary, NC: Reliably commute or planning to relocate before starting work (Required)
Experience:
- validation: 1 year (Preferred)
Work Location: One location
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