Solid Dose Manufacturing Tech (cGMP)

VetJobs; New London (CT); On-site; USD 33,000 - 56,000; Full time

Job summary

Pfizer in Groton, CT is seeking a Technical Associate for the SDM Operations Group to support batch-process manufacturing of solid dose formulations. The role emphasizes compliance with cGMP guidelines, setup and operation of complex equipment, and daily documentation in a regulated manufacturing environment.

The position requires 2+ years in biotech manufacturing or a related lab setting, strong teamwork, and solid computer skills.

Qualifications

• High School Diploma or GED.
• 2+ years of cGMP experience.
• Experience in a biotechnology manufacturing or laboratory environment.
• Operational knowledge of multiple computerized systems.
• Familiarity with Production Control Systems, ERP systems and other business systems.
• Maintains a safe work environment.
• Demonstrated capability to work as a team member in a matrix development team.
• Excellent oral and written communication skills.
• Strong computer skills in Microsoft Office required, especially MS Word, MS Excel.

Responsibilities

• Manufacture solid dosage forms (tablets and capsules) for developmental, stability and clinical studies/supplies.
• Set-up, operate, clean, and maintain complex pharmaceutical manufacturing equipment associated with Solid Dose processing using closed transfer systems.
• Implement cGMP procedures and safe handling techniques for solid dosage processing.
• Generate, assist and execute documentation such as working batch records, logbooks, labels and in-process run sheets.
• Proficient use of digital tools and paperless systems (e.g., OpsTrakker).
• Create and revise SOPs for cGMP manufacturing equipment and activities.
• Assist with Quality Compliance reviews and investigations; identify CAPAs.
• Complete operator care tasks for maintenance and operation of SDM equipment.
• Operate and maintain the SDM cGMP manufacturing space.
• Compute yield, batch accountability, and process ranges using mathematical tools.
• Identify and lead Lean-based continuous improvement projects.

Skills

Communication skills

Teamwork

MS Word

MS Excel

cGMP experience

Biotech manufacturing experience

Education

High School Diploma or GED

Bachelor's Degree (Nice-to-have)

Tools

ERP Systems

Job description

Pfizer in Groton, CT is seeking a Technical Associate for the SDM Operations Group to support batch-process manufacturing of solid dose formulations. The role emphasizes compliance with cGMP guidelines, setup and operation of complex equipment, and daily documentation in a regulated manufacturing environment.

The position requires 2+ years in biotech manufacturing or a related lab setting, strong teamwork, and solid computer skills.