Lead, Early-Phase GMP Product Development

Staffing Resource Group, Inc; Tampa (FL); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

Relocation assistance

Medical insurance

Dental insurance

Vision insurance

Job summary

Staffing Resource Group, Inc. is seeking a Manager, Product Development GMP Operations in Tampa, FL to lead early-phase drug product manufacturing and packaging initiatives.

The role focuses on building GMP capabilities, guiding multidisciplinary teams, and ensuring compliant, scalable operations for clinical supply. The position offers direct-hire employment, on-site work, and a comprehensive package including competitive benefits.

Qualifications

• Significant experience in early phase GMP drug product manufacturing and/or packaging.
• 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

Responsibilities

• 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 leadership and administrative management for a diverse technical team, including performance reviews, coaching, training, and career development
• 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

Education

Bachelor's or Master’s degree in a scientific field

PhD (advantageous)

Job description

Staffing Resource Group, Inc. is seeking a Manager, Product Development GMP Operations in Tampa, FL to lead early-phase drug product manufacturing and packaging initiatives.

The role focuses on building GMP capabilities, guiding multidisciplinary teams, and ensuring compliant, scalable operations for clinical supply. The position offers direct-hire employment, on-site work, and a comprehensive package including competitive benefits.