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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing qualification and validation programs within the pharmaceutical industry, with a strong focus on compliance with FDA and cGMP requirements. Proven ability to lead teams, solve complex problems, and develop technical documentation.
Highest-signal resume keywords
Validation ManagementPharmaceutical Industry ExperienceSupervisory ExperienceValidation TechniquesFDA and 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
Qualification and ValidationValidation ProcessesTechnical DocumentationProject ManagementProblem Solving
Soft Skills
Excellent Written CommunicationExcellent Oral Communication
Industry Keywords
PharmaceuticalQuality AssuranceOperationsContinuous ImprovementAudit and Inspection
About the role
Key responsibilities & impact- Manage the Qualification and Validation program
- Oversee all activities of the Validation team
- Lead a group of colleagues in designing, managing, and executing projects
- Manage qualification and validation of manufacturing and packaging equipment and processes for over-the-counter semi-solid creams, ointments and gels, suppositories, and nasal sprays
- Oversee Validation Engineers performing qualification and validation activities at the Perrigo New York facility
- Determine validation requirements for complex operational issues
- Evaluate, design, develop, and coordinate key projects
- Develop and write technical documents
- Lead efforts to solve complex problems and achieve goals
- Identify and lead cross-functional departments to drive compliance and continuous improvement initiatives
- Provide audit and agency inspection reports related to validation requirements and activities
Requirements
What you’ll need- Bachelor degree in scientific field combined with five or more years of progressively responsible experience of greater breadth and/or depth
- Pharmaceutical industry experience
- Supervisory experience required
- Experience in Validation, Quality, or Operations required
- Thorough understanding of validation processes and interpretation and application of FDA and cGMP requirements
- Demonstrated ability in validation techniques, practices, precedents, theory, and principles
- Excellent written and oral communication skills
- All application materials, including resumes and CVs, must be submitted in English
Benefits
Comp & perks- Competitive compensation
- Benefits tailored to supporting you and your family
- Career development opportunities
- Total Rewards program