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QA/RA Director
PerkinElmerProvides strategic quality and regulatory compliance leadership at Project Farma in high-impact life sciences projects. Mentoring consultants and managing client engagements with a focus on quality systems.
Posted 5/31/2026full-timeRemote • North Carolina • 🇺🇸 United StatesLead💰 $165,000 - $200,000 per yearWebsite
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Quality Management Systems (QMS)GxPregulatory frameworksdata integrityrisk managementcompliance transformationsupplier quality auditsnew product introductioninspection readinessmock inspections
Soft Skills
mentoringcoachingcommunicationcollaborationstrategic planningexecutive presencebusiness developmentpresentation skillsleadershipproblem-solving
Certifications & Qualifications
industry-specific certifications
Industry Keywords
life sciencesregulatory rolesFDAEMAMHRAICHWHOquality system initiativesconsulting environmentthought leadership
About the role
Key responsibilities & impact- Serve as a senior advisor and delivery leader on strategic quality and regulatory engagements
- Design and remediate Quality Management Systems (QMS)
- Conduct inspection readiness and mock inspections
- Provide regulatory responses and training
- Manage data integrity, risk management, and compliance transformation
- Oversee investigation responses and submission support
- Lead supplier quality audits and new product introduction development
- Mentor and coach consultants and project Directors within Quality & Regulatory practice
- Collaborate with internal teams for resource alignment and strategy planning
Requirements
What you’ll need- Bachelor’s degree in scientific, regulatory, engineering, or related discipline preferred
- 16 years (Director) – 20 years (Sr. Director) of experience in life sciences quality, compliance, or regulatory roles
- Demonstrated success delivering and advising on complex GxP, regulatory, and quality system initiatives
- Strong working knowledge of global regulatory frameworks (FDA, EMA, MHRA, ICH, WHO)
- Proven ability to support sales and business development in a consulting environment
- Executive presence with strong written and verbal communication skills
- Willingness and ability to travel regularly in support of project delivery and client needs
- Previous experience in development and presentation of thought leadership including conference presentations, white papers, published papers, etc.
- Advanced Degree preferred
- One or more industry-specific certifications
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Professional development opportunities
- Travel allowances