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Quality Facilities and Equipment Validations Specialist
Strive Compounding Pharmacy. Own and maintain the Master Validation Plan .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in validation processes, including equipment qualification, IQ/OQ/PQ, and regulatory compliance within the pharmaceutical and life sciences sectors. Proven ability to develop and manage validation documentation while providing technical guidance and training.
Highest-signal resume keywords
Master Validation Plan ManagementEquipment Qualification and RequalificationValidation Documentation DevelopmentTechnical WritingGMP/cGMP Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
IQ/OQ/PQValidation Lifecycle ManagementTemperature MappingFacility CertificationShipping ValidationValidation ProtocolsAnalytical SkillsProject Management
Soft Skills
Organizational SkillsIndependent WorkTechnical Guidance
Industry Keywords
PharmaceuticalSterile CompoundingLife SciencesRegulated Environment
About the role
Key responsibilities & impact- Own and maintain the Master Validation Plan
- Manage equipment qualification and requalification programs, including IQ/OQ/PQ
- Oversee temperature mapping, facility certification, and shipping validation activities
- Develop and maintain validation protocols, reports, schedules, and supporting documentation
- Identify validation gaps and ensure corrective actions are completed
- Track requalification and certification requirements to prevent missed deadlines
- Partner with Quality, Pharmacy, Operations, Facilities, Engineering, and other teams
- Support regulatory inspections and provide validation documentation and technical expertise
- Provide validation-related training and technical guidance
- Support validation of new equipment, systems, processes, and facilities
- Build internal validation expertise and reduce reliance on external consultants
Requirements
What you’ll need- 5+ years of experience in pharmaceutical, sterile compounding, GMP/cGMP, life sciences, or another highly regulated environment
- Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related field
- Ability to travel up to 25% to internal facilities and industry conferences
- Proven track record of technical writing
- Hands-on experience with equipment qualification and validation
- Strong understanding of IQ/OQ/PQ and validation lifecycle management
- Experience developing or managing validation documentation
- Strong organizational, analytical, documentation, and project management skills
- Ability to work independently and serve as a technical resource for validation activities
Benefits
Comp & perks- Employer-paid healthcare coverage, effective the 1st day of the following month of your hire date
- Free Strive compounded medications for employees based on a valid patient-specific prescription from a licensed healthcare provider
- Paid time off
- Sick time
- FSA and HSA options
- Parental leave
- 401(k) with employer matching
- Life insurance
- Vision and dental insurance
- Veterinary insurance
- Collaborative, engaging workplace with opportunities to connect, celebrate, and build meaningful relationships
- Support for personal and professional growth