Key Responsibilities:
- Scope client requirements and design tailored program plans focused on audit execution, compliance, and operational outcomes.
- Manage client-facing programs across all product stages—from clinical to post-market surveillance.
- Execute supplier qualification, validation, and maintenance programs.
- Conduct qualification and technical visits to vendor sites and provide supplier risk recommendations.
- Lead cross-functional teams in delivering GxP-compliant quality programs, including: deviation and change control, laboratory controls, process validation, equipment qualification, and CAPA.
- Create and maintain Quality and Technical Agreements in alignment with EU/FDA and global regulatory standards.
- Provide structured business planning to drive measurable program success and identify growth opportunities.
- Conduct data-driven program reviews and client presentations.
- Ensure SQA programs evolve with changing regulatory expectations.
Required Qualifications:
- Bachelor’s or advanced degree in a scientific or engineering discipline.
- Extensive GxP knowledge, with experience supporting programs from clinical development through post-market stages.
- Strong understanding of international regulatory compliance (EU, FDA, etc.).
- Demonstrated ability to scope client needs and convert them into effective programs.
- Experience managing audit-based programs and cross-functional quality initiatives.
- Managerial or higher-level leadership experience in field services or operations.
- Strong background in supplier quality, quality systems, and laboratory environments.
- 30% domestic and international travel
Preferred Qualifications
- Prior experience leading or supporting service-oriented client engagements.
- Experience in commissioning and equipment validation projects.
- Background as a laboratory director or in lab operations oversight.
- Experience in solid dose manufacturing, aseptic processes, and laboratory controls.
- Exposure to special services such as qualification, maintenance, and facility validation.
- Operational leadership in pharmaceutical environments.
- Established industry relationships and familiarity with potential clients.
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What We Do
Welcome to the SQA Services, Inc. home on LinkedIn! Follow us to stay up to date on all things quality - including industry events, news, and ways to get involved with #TeamSQA. Also, keep an eye out for job postings! SQA is always looking for quality professionals and new team members!
WHAT IS SQA SERVICES, INC.?
SQA provides global supplier quality services for quality-critical industries. With quality, manufacturing, and regulatory experts located in over 50 countries, SQA provides a cost-effective, local supplier presence.
Managed, on-demand services include supplier quality audits, supplier remediation, quality engineering, source inspection, corrective action management, and real-time supplier quality data via SQA's world-class STEPQ technology.
HOW CAN I GET IN TOUCH WITH SQA?
We look forward to connecting with you and discovering how Team SQA can help you and your team reach your quality goals. Contact our team by heading over to http://www.sqaservices.com/contact
If you think you or someone you know would be a great fit for our team, please send your resume to our Associate Development team at: [email protected]

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