Senior Validation Specialist
Senior Validation Specialist
GxPeople Global
New Hampshire, United States
See who GxPeople Global has hired for this role
GxPeople are working with a major player in the biopharmaceutical sector on an exciting opportunity for a skilled Lead Validation Engineer with experience working with QC laboratory Computer Systems and Instruments.
Senior Lead QC System Validation
Key Responsibilities:
- Completes QC analytical instrument and software validation tasks, including writing GMP procedures, validation documents, and executing test scripts.
- Serves as a leader for the team, drafting, reviewing, and approving QC analytical instrument and software validation project plans.
- Manages projects independently to ensure timely completion.
- Handles software administration duties, including converting test methods, batch records, and other written documents into instrument computer system software.
- Performs user and application software administration on Enterprise systems, including system audit trail reviews, monitoring backups, and performing validation maintenance on systems.
- Recommends and implements engineering controls for analytical instruments and software in QC Laboratories. May act as an ACSV SME during regulatory and customer inspections and audits.
- Manages all aspects of QMS processes, including Change Control, Deviations, CAPAs, and Tasks. Writes, reviews, assesses, and/or approves change controls for analytical instruments and software used in QC laboratories and manufacturing.
- Ensures data integrity and compliance with company SOPs and specifications, FDA, and cGMP regulations.
- Identifies and addresses compliance gaps as needed.
- Performs other duties as assigned.
Key Requirements:
- Bachelor’s Degree required, preferably in Microbiology, Biochemistry, Chemistry, Engineering, Computer Science, or related science fields.
- Minimum of 5-7 years of experience in Analytical Laboratory Computer Systems and Instrument Validation.
- At least 5 years of experience administering local systems, preferrably TOC and Softmax.
- Proficient in problem-solving and critical thinking.
- Strong understanding of regulatory requirements.
- Experience in data integrity and SDLC life cycle.
- Experience working in a Quality Control Laboratory or with enterprise computer systems, and GMP Quality Systems such as TrackWise, LIMS, LES, Empower, and MODA.
- Previous project management experience.
*This role is only open to candidates with a current US working visa*
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Seniority level
Associate -
Employment type
Full-time -
Job function
Quality Assurance -
Industries
Pharmaceutical Manufacturing
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