Join to apply for the Staff Validation Engineer role at Performance Validation
1 day ago Be among the first 25 applicants.
About Us
Here at Performance Validation, Inc (PV), we have been providing Commissioning, Qualification, and Validation services to the life science industries for over 30 years! We are a 100% employee-owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, supporting clients throughout the US and overseas. PV is committed to providing growth opportunities through professional development, new services, and expanding into new geographical areas.
About The Job
Performance Validation is seeking a full-time Level I Validation Engineer / Specialist to join our teams in Indiana, Michigan, Illinois, Kansas, and North Carolina. The engineer will report to the Division Director or Manager and be assigned to project teams led by a Project Leader.
Responsibilities
- Develop understanding of technical, quality, and scientific principles to meet industry and customer requirements.
- Collaborate in a team environment to meet objectives within established timelines.
- Create verification / qualification deliverables such as Requirements Documents, Specifications, Test Protocols (IQ / OQ / PQ), and Summary Reports.
- Execute test protocols, identify and resolve non-conformances / deviations.
- Manage change control activities across multiple projects.
Education & Requirements
Bachelor's degree (BS / BA) or three years of experience in pharmaceutical or a regulated industry, not necessarily in validation.Preferred degrees in Biomedical, Chemical, or Mechanical Engineering.Experience & Skills
Self-motivated with professionalism, enthusiasm, and ability to work independently.Strong interpersonal skills for confident interaction with clients and team members.Excellent communication skills with high attention to detail.Proficiency with Microsoft Word and Excel.What We Offer
Competitive salary, profit sharing, stock ownership, 401(k) match.Paid vacation, holidays, training, health coverage, insurance, stipends, and growth opportunities.Team building activities and a collaborative work environment.Work / life balance and up to 20% travel availability.Qualified candidates must be authorized to work in the US; sponsorship is not provided.
Additional Details
Seniority level : Entry levelEmployment type : Full-timeJob function : Quality AssuranceIndustry : Pharmaceutical ManufacturingJ-18808-Ljbffr