PV
Validation Engineer
Accepting applicationsPerformance Validation · Raleigh, NC
Full-Time Associate aiarmateganperl
Posted
1 May
Category
Test
Experience
Associate
Country
United States
About Us
Here at Performance Validation, Inc (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for 37 years. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About The Job
Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Raleigh, NC The Level II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams headed by a Project Leader.
Responsibilities
Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements
Work in a team environment to meet defined objectives based on established timelines
Develop verification/qualification deliverables including but not limited to Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports
Execute test protocols, including identification and resolution of non-conformances/deviations
Track and manage change control activities for multiple concurrent projects
Requirements you will need
Education
BS/BA degree and 1-2 years in pharmaceutical or other regulated industry experience directly related to pharmaceutical validation
BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering preferred
Experience
Change and Deviation Management
Strong interpersonal skills. Must interact confidently with clients, other contractors, and employees
Possess excellent oral and written communication skills and high attention to detail
Cleaning, Sterlization, and Decontamination Validation experienced preferred
Device Assembly and Packing experience preferred
What We Have To Offer
Competitive base salary
Biannual profit share
Employee stock ownership program
401(k) company match
Flexible time off policy
Paid Parental Leave
Internal and external training opportunities
Medical, vision, and dental coverage
Disability and life insurance
Cellphone stipend
Growth opportunities
Company-sponsored team building outings
A collaborative work environment
Work/life harmony
This role involves frequent travel to client and partner sites, estimated at 30–50% depending on business needs and project cycles.
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation, Inc. does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Show more Show less
Here at Performance Validation, Inc (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for 37 years. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About The Job
Performance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Raleigh, NC The Level II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams headed by a Project Leader.
Responsibilities
Develop a sound understanding of how to properly implement technical, quality, and scientific principals necessary to meet industry and customer requirements
Work in a team environment to meet defined objectives based on established timelines
Develop verification/qualification deliverables including but not limited to Requirements Documents, Functional and Design Specifications, Test Protocols (IQ/OQ/PQ), and Summary Reports
Execute test protocols, including identification and resolution of non-conformances/deviations
Track and manage change control activities for multiple concurrent projects
Requirements you will need
Education
BS/BA degree and 1-2 years in pharmaceutical or other regulated industry experience directly related to pharmaceutical validation
BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering preferred
Experience
Change and Deviation Management
Strong interpersonal skills. Must interact confidently with clients, other contractors, and employees
Possess excellent oral and written communication skills and high attention to detail
Cleaning, Sterlization, and Decontamination Validation experienced preferred
Device Assembly and Packing experience preferred
What We Have To Offer
Competitive base salary
Biannual profit share
Employee stock ownership program
401(k) company match
Flexible time off policy
Paid Parental Leave
Internal and external training opportunities
Medical, vision, and dental coverage
Disability and life insurance
Cellphone stipend
Growth opportunities
Company-sponsored team building outings
A collaborative work environment
Work/life harmony
This role involves frequent travel to client and partner sites, estimated at 30–50% depending on business needs and project cycles.
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation, Inc. does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
Show more Show less
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