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Associate Validation Scientist
Perrigo Company plcAssociate Validation Scientist preparing validation protocols and overseeing operations for Perrigo infant formula. Coordinates cross-departmental efforts and manages compliance in manufacturing processes.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in validation protocols and standard operating procedures within regulated environments, particularly in food and pharmaceutical sectors. Proficient in managing validation activities, including Computer System Validation and compliance with relevant regulations.
Highest-signal resume keywords
Validation Protocol DevelopmentQuality Assurance ExperienceRegulated Food ManufacturingHACCP Study SupportTechnical Writing in FDA Regulated Industry
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Validation ResponsibilitiesCCP and OPRP TestingCleaning VerificationsComputer System ValidationProcess Flow ReviewsAnnual Verification ActivitiesLean ManufacturingFSSC22000/SQF Regulations21 CFR ComplianceTechnical Writing
Soft Skills
Excellent Communication SkillsAbility to Work IndependentlyMulti-Priority Management
Tools & Technologies
Microsoft AccessMicrosoft ExcelMicrosoft WordMicrosoft PowerPoint
Industry Keywords
Infant Formula OperationsQuality ExperienceFood ManufacturingPharmaceutical IndustryMedical Device Field
About the role
Key responsibilities & impact- Prepare and maintain validation protocols and validation standard operating procedures for Perrigo Infant Formula operations.
- Coordinate with personnel from other departments, such as Quality Assurance, Production, Technical, and Engineering.
- Perform/manage annual CCP and OPRP testing as well as the annual cleaning verifications.
- Oversee all Computer System Validation protocol approvals and executions.
- Support HACCP study, process flow and QMS reviews.
- Assist in the HACCP study completion on a timely basis.
- Perform annual verification activities, including CIP and CCP/OPRP verifications.
Requirements
What you’ll need- Bachelor’s Degree in Engineering, Chemistry, Microbiology, or related field or equivalent work experience in a validation scientist role
- Minimum of 3-5 years of related Quality experience
- Experience with validation responsibilities in food, pharmaceutical, or medical device field
- Experience in regulated food manufacturing environment with exposure to 21 CFR 117, lean manufacturing, FSSC22000/SQF regulations and preferred experience with 21 CFR 106/107 and 21 CFR 113.
- Excellent written and oral communication skills, including report writing
- Ability to work independently and handle multiple priorities
- Proficiency with PCs and software such as Access; Excel; Word; PowerPoint; Technical writing ability in an FDA regulated industry
Benefits
Comp & perks- Competitive compensation
- Career development opportunities