GMP Central Services Technician II

Catalent Pharma Solutions; Harmans (MD); On-site; USD 33,000 - 39,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Tuition Reimbursement

Paid time off

8 paid holidays

Job summary

Catalent Pharma Solutions seeks a Technician II, Central Services to support GMP manufacturing from Harmans, MD. The role involves maintaining batch records, authoring SOPs, and enabling smooth tech transfer with Process Development and MS&T.

You’ll investigate deviations, troubleshoot equipment, and work with facilities and QA to ensure compliant operations. Ideal candidates have GMP experience, strong documentation skills, and the ability to collaborate across teams.

Qualifications

• Strong knowledge and ability to apply scientific principles to solve operational tasks.
• Excellent documentation skills including creation and review of batch records and SOPs.
• Understanding of GMP compliance and safety procedures.

Responsibilities

• Maintain batch production records and GMP documentation per SOPs.
• Support technology transfer with Process Development and MS&T teams.
• Lead deviations and CAPAs and perform root cause investigations.
• Troubleshoot processes and coordinate with facilities and engineering teams.
• Collaborate with production leadership to optimize manufacturing processes.
• Assist in procurement and equipment qualification during campaigns.
• Participate in facility expansion and continuous improvement initiatives.
• Perform cleaning and maintenance of manufacturing equipment and environments.
• Provide cross-functional technical support during campaigns.

Skills

GMP compliance

Documentation skills

Team collaboration

Root cause investigations

Microsoft Office

Education

Bachelor’s degree in Scientific/Engineering/Biotech

Associate degree in Scientific/Engineering/Biotech

High School diploma or GED

Tools

Microsoft Office

Job description

Catalent Pharma Solutions seeks a Technician II, Central Services to support GMP manufacturing from Harmans, MD. The role involves maintaining batch records, authoring SOPs, and enabling smooth tech transfer with Process Development and MS&T.

You’ll investigate deviations, troubleshoot equipment, and work with facilities and QA to ensure compliant operations. Ideal candidates have GMP experience, strong documentation skills, and the ability to collaborate across teams.