Validation Engineer at PerfVal Labs, Inc.

Pleasant Prairie, Wisconsin, United States -

Full Time

Start Date

Immediate

Expiry Date

14 Oct, 26

Salary

0.0

Posted On

16 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmaceutical Validation, IQ/OQ/PQ, Test Protocol Execution, Change Control Management, Technical Writing, Microsoft Word, Microsoft Excel, Interpersonal Communication, Non-conformance Resolution, Requirements Documentation

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 or Senior Validation Engineer to join our team in Pleasant Prairie, WI. The Level II/III Validation Engineer/Specialist reports directly to the Project Leader 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 minimum of 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: * Self-starter who exhibits a professional demeanor, enthusiasm, and ability to work independently with minimal supervision * Strong interpersonal skills. Must interact confidently with clients, other contractors, and employees * Possess excellent oral and written communication skills and high attention to detail * Experience with office word-processing and spreadsheet programs such as Microsoft Word and Excel 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 balance 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 status) for this employment position.

Responsibilities

Develop and execute verification and qualification deliverables, including test protocols and summary reports. Manage change control activities and resolve non-conformances to meet industry and customer requirements.