Insight Global
Insight Global is hiring a Validation Engineer in Massachusetts to support their client. This position is based on site and requires the engineer to interface with manufacturing equipment, medical device products, and cross‑functional partners.
Daily tasks in this role include:
Developing, writing, reviewing, maintaining and revising manufacturing documentation such as process work instructions, manufacturing specifications, and inspection procedures to support product manufacturing.
Supporting the development and execution of manufacturing equipment qualifications (URS/FAT/SAT/IQ).
Supporting the development and execution of process validations (OQ/PQ/PV).
Developing, writing, and reviewing various validation deliverables such as CSV‑E, engineering studies, etc.
Partnering with cross‑functional partners to ensure a sound validation strategy and smooth transitions to production go‑live.
Ensuring adequate documentation within the Quality System.
Responsible for equipment design, implementation, and validation.
Required Skills & Experience
3+ years of experience in validation for medical devices or regulated equipment.
Experience in validation of medical device equipment and OQ/PQ/PV.
Strong understanding of manufacturing equipment qualification (URS/FAT/SAT/IQ).
Nice to Have Skills & Experience
Experience at Johnson & Johnson or similar with a focus on CMM validation or foundry processes.
Base Pay Range $45.00/hr - $55.00/hr
Employment Type Contract
Seniority Level Associate
Benefits
Medical insurance
401(k) retirement plan
Vision insurance
Get notified about new Validation Engineer jobs in
Raynham, MA .
#J-18808-Ljbffr
Daily tasks in this role include:
Developing, writing, reviewing, maintaining and revising manufacturing documentation such as process work instructions, manufacturing specifications, and inspection procedures to support product manufacturing.
Supporting the development and execution of manufacturing equipment qualifications (URS/FAT/SAT/IQ).
Supporting the development and execution of process validations (OQ/PQ/PV).
Developing, writing, and reviewing various validation deliverables such as CSV‑E, engineering studies, etc.
Partnering with cross‑functional partners to ensure a sound validation strategy and smooth transitions to production go‑live.
Ensuring adequate documentation within the Quality System.
Responsible for equipment design, implementation, and validation.
Required Skills & Experience
3+ years of experience in validation for medical devices or regulated equipment.
Experience in validation of medical device equipment and OQ/PQ/PV.
Strong understanding of manufacturing equipment qualification (URS/FAT/SAT/IQ).
Nice to Have Skills & Experience
Experience at Johnson & Johnson or similar with a focus on CMM validation or foundry processes.
Base Pay Range $45.00/hr - $55.00/hr
Employment Type Contract
Seniority Level Associate
Benefits
Medical insurance
401(k) retirement plan
Vision insurance
Get notified about new Validation Engineer jobs in
Raynham, MA .
#J-18808-Ljbffr