What are the responsibilities and job description for the Validation Engineer position at PSC Biotech?
POSITION SUMMARY:
The Validation Engineer is responsible for ensuring systems, facilities, and equipment meet design requirements to be put in place for a facility with assistance from upper management. 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”.
DUTIES AND RESPONSIBILITIES:
- Support commission, qualify, and validate facilities, utilities, and/or equipment in assigned projects.
- Ability to follow instructions of controlled documents for CQV projects.
- Assist review and qualify equipment for commissioning, qualification, and validation activities.
- Collaborate with multiple departments on assigned project activities and deliverables.
- Assist in coordination of execution of FAT/SAT, IQ, OQ, and PQ.
- Assist 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
REQUIRED EDUCATION AND WORK EXPERIENCE:
- Bachelor’s Degree in Engineering or Life Science or equivalent degree.
- 1-3 years of applicable work experience in a GMP sector in similar role.
- Experience executing DQ, FAT, SAT, IQ, OQ, PQ, and PV documents.
- 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.
- Excellent written and verbal communication skills.
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