- Execute startup CQV activities involving the commissioning and qualification of pharmaceutical lab and manufacturing equipment and computer systems.
- Execution of CQV validation protocols specific to manufacturing, including IQ, OQ, and PQ of lab and manufacturing equipment and computer systems.
- Complete appropriate cGMP documentation throughout validation life-cycle
- Technical writing
- 1+ years' experience of equipment validation in pharmaceutical industry
- Experience with leading/executing CQV validation projects
- Bachelor's degree in related field
- 60,000-90,000 based on experience
- Attractive employee benefits package, 401K , PTO, travel expenses paid
- No Corp to Corp available.
- 401(k)
- Dental/Health/Vision insurance
- Paid time off
- Relocation Assistance
- Immigration/visa sponsorship available
- 8 hour shift
- Day shift
- Monday to Friday
- Multiple locations/Nationwide Client Sites
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Spectraforce Technologies Lansdale, United StatesTitle: Validation Engineer · Location: West Point, PA 19486 · Duration: 6 Months · Qualifications: · Associate's degree or higher preferred with 1-2 years of experience or 4-5 years working experience in metrology/information technology / customer service or other relevant field. ...
Validation Engineers - Philadelphia, United States - STELLAR CONSULTING GROUP LLC
Description
Job Description
Job DescriptionValidation Associates is currently in search of Validation Engineers for our pharmaceutical clients nationwide, Multiple positions
All Visas Accepted- OPT/CPT/GC/USC/TN/L2- Multiple Positions- Nationwide. (US Candidates only)
We are actively looking for fresh graduates & undergraduates with specialization in Biotechnology, Regulatory, Biomedical, Biochemistry, Chemical, Pharmacy, Chemistry, healthcare or any related life science field.
Responsibilities of the Validation Engineer include-
Qualifications of the Validation Engineer include:-
Compensation for the Validation Engineer include:-
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
Job Type: Full-time
Benefits:-
Schedule:-
Work Location:-