Senior Commissioning Qualification Validation Engineer
Senior Commissioning Qualification Validation Engineer
Posted on :
12-08-2025
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1 Vacancy
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Job Description
POSITION SUMMARY:
The Senior Commissioning Qualification and Validation (CQV) Engineer is responsible for ensuring systems facilities and equipment meet design requirements to be put in place for a facility. The incumbent is also responsible and accountable for the execution of the PSC mission to maintain the integrity and professionalism of our products and services while enabling steady growth and development.
- Act as a lead and simplify CQV functions reports and processes.
- Support implementing safety programs for major capital projects.
- Commission qualify and validate facilities utilities and/or equipment in assigned projects.
- Initiates authors revises reviews and completes controlled documents for CQV projects.
- Review and qualify equipment for commissioning qualification and validation activities.
- Writes and reviews GMP and GDP documents and technical specifications.
- Collaborate with multiple departments on assigned project activities and deliverables.
- Initiate and coordinate risk analyses design reviews execute FAT/SAT IQ OQ and PQ
- Contact and work with contractors and vendors on assigned projects.
- Ability to travel as needed.
- Additional duties and responsibilities may be assigned from time-to-time.
Requirements
- Bachelor s Degree in Engineering or Life Science.
- 7-10 years of applicable work experience in the biomedical and pharmaceuticals industry.
- Proficient in authoring and executing DQ FAT SAT IQ OQ PQ and PV documents.
- Proficient in developing SOPS final reports and validation & quality policies.
- Strong experience developing and executing CQV protocols.
- Strong experience creating and maintaining CQV policies and processes.
- Has good understanding and complies to cGMPs and CFR21 Part 11 guidelines.
- Demonstrated strategic thinking and implementation skills; proven analytical skills with ability to translate. Data to actionable plans; demonstrated ability to develop and implement marketing and product/service. strategies by converting them into tactical marketing plans; execute and deliver results.
- Excellent presentation and communication skills written and oral for a variety of audiences.
- Highly organized in planning and time management with the ability to multi-task.
7-10 years of applicable work experience in the biomedical and pharmaceuticals industry. Proficient in authoring and executing DQ, FAT, SAT, IQ, OQ, PQ, and PV documents. Proficient in developing SOPS, final reports and validation & quality policies. Strong experience developing and executing CQV protocols. Strong experience creating and maintaining CQV policies and processes. Has good understanding and complies to cGMPs and CFR21 Part 11 guidelines. Demonstrated strategic thinking and implementation skills; proven analytical skills with ability to translate. data to actionable plans; demonstrated ability to develop and implement marketing and product/service. strategies by converting them into tactical marketing plans; execute and deliver results. Excellent presentation and communication skills, written and oral, for a variety of audiences. Highly organized in planning and time management, with the ability to multi-task.
Education
Bachelor s Degree in Engineering or Life Science.
Employment Type
Full Time
Company Industry
Key Skills
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