Validation Specialist
PharmEng TechnologyPortsmouth, New Hampshire, United States
Posted December 12, 2025
Full Time
About the Company
PharmEng Technology, now part of the Efor Group, delivers specialized compliance engineering services—Commissioning, Qualification, and Validation (CQV)—to the pharmaceutical, biotechnology, and healthcare sectors, drawing on 25 years of industry expertise. The firm designs, constructs, and validates facilities, utilities, equipment, and computer systems in strict adherence to cGMP, GEP, and GLP, covering areas such as API production, laboratory, and medical device manufacturing. Leveraging Efor’s global network of 3,000 experts across 12 countries, PharmEng combines worldwide best practices with local proximity to offer flexible, innovative, and cost‑effective solutions that meet regulatory and business demands. Its culture prioritizes quality, safety, and client partnership, ensuring customized, measurable outcomes for leading industry players.
Job Description
The Analytical Validation Specialist III will assist in validation activities, including software updates, new system introduction, and decommissioning of analytical systems.
Requirements
- Bachelor's degree in Chemistry, Biochemistry, or related field
- Minimum of 5 years of experience in analytical validation or related field
- Strong understanding of validation principles and regulatory requirements
- Excellent analytical and problem-solving skills
- Strong attention to detail and ability to work independently and as part of a team
- Effective communication and interpersonal skills