Validation Engineer at PerfVal Labs, Inc.

Raleigh, North Carolina, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Jul, 26

Salary

0.0

Posted On

14 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation, Commissioning, Qualification, Change management, Deviation management, IQ/OQ/PQ, Technical writing, Functional specifications, Design specifications, Cleaning validation, Sterilization, Decontamination, Device assembly, Packing, Pharmaceutical industry, Regulatory compliance

Industry

Pharmaceutical Manufacturing

Description

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.

Responsibilities

The Validation Engineer will develop verification and qualification deliverables such as test protocols and summary reports while ensuring compliance with industry standards. They are also responsible for executing test protocols, managing deviations, and overseeing change control activities across multiple projects.