Product Development GMP Operations Lead
Posted: 08/12/2026
Employment Type:
Direct Hire
Division: Life Sciences
Job Number: JN -082026-21331
State: Florida
Job Description
Product Development GMP Operations Lead
Location: Tampa, FL
Industry: Pharmaceutical
Hours: M-F, 8am-5pm, on-site 100%
Salary: Competitive industry compensation package (relocation assistance offered for the right candidate)
Employment Type: Direct hire
Company overview:
We are a manufacturing site specializes in cGMP formulation development, clinical supply, and commercial manufacturing for oral solid dosage and inhalation products. The site supports customers throughout the drug development lifecycle while offering employees the opportunity to work with advanced technologies in a collaborative, quality-driven environment that directly impacts patient health worldwide.
This individual is a site based leadership role supporting early phase clinical trial drug product manufacturing and packaging. This position offers the opportunity to design and lead GMP capabilities, guide multidisciplinary teams, and directly contribute to bringing innovative therapies into the clinic.
Responsibilities:
Qualifications:
ADA/EOE
IND123
Location: Tampa, FL
Industry: Pharmaceutical
Hours: M-F, 8am-5pm, on-site 100%
Salary: Competitive industry compensation package (relocation assistance offered for the right candidate)
Employment Type: Direct hire
Company overview:
We are a manufacturing site specializes in cGMP formulation development, clinical supply, and commercial manufacturing for oral solid dosage and inhalation products. The site supports customers throughout the drug development lifecycle while offering employees the opportunity to work with advanced technologies in a collaborative, quality-driven environment that directly impacts patient health worldwide.
This individual is a site based leadership role supporting early phase clinical trial drug product manufacturing and packaging. This position offers the opportunity to design and lead GMP capabilities, guide multidisciplinary teams, and directly contribute to bringing innovative therapies into the clinic.
Responsibilities:
- An agile career with opportunities for growth in a dynamic Product Development environment
- A collaborative, inclusive, and ethical workplace culture
- Compensation programs that recognize high performance and leadership impact
- Competitive medical, dental, and vision insurance coverage
- Access to our learning, development, and leadership programs
- Lead and develop Product Development GMP manufacturing and packaging operations supporting early phase clinical trial drug products
- Design, oversee, and maintain PD GMP spaces, including equipment selection, engineering build outs, and approval of engineering drawings
- Serve as the technical and operational SME for PD GMP activities, supporting projects, new technologies, and strategic growth initiatives
- Provide technical leadership and guidance to multidisciplinary teams supporting Product Development GMP operations, including coaching, training, knowledge sharing, and coordination of resources and priorities.
- Ensure compliance with cGMPs, SOPs, safety standards, and regulatory requirements, maintaining inspection readiness at all times
- Act as a key internal and external stakeholder, participating in regulatory audits, client meetings, and on site visits
- Coordinate closely with engineering, quality, manufacturing, and project teams to ensure timely, compliant, and cost effective delivery of work
Qualifications:
- Significant experience in early phase GMP drug product manufacturing and/or packaging within a pharmaceutical or life sciences environment
- OSD (oral solid dosage) experience is a must
- Strong understanding of cGMP regulations, quality systems, regulatory inspections, and audit readiness
- Proven ability to lead technical teams, manage resources, resolve complex issues, and deliver results through others
- Experience designing or supporting GMP facilities, including collaboration with engineering and oversight of build out activities
- Effective communication and stakeholder management skills, including customer facing and cross functional collaboration
- A scientific degree or similar field required, with an emphasis on applying knowledge to advance drug product development
- Approximately 15+ years of relevant experience with a bachelor s or master s degree, or 10+ years with a PhD
ADA/EOE
IND123
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