GMP Manufacturing Operator - Pharma Production & Quality

Actalent; New Jersey; On-site; USD 42,000 - 62,000; Full time

Job summary

Actalent in New Jersey seeks a Manufacturing Operator to join a fast-paced pharmaceutical operation. You will operate manufacturing equipment, document processes meticulously, and collaborate with quality, maintenance, and development teams to produce clinical supplies and support development experiments.

Responsibilities include following SOPs and GDP, setting up lines, performing changeovers, conducting in-process inspections, and using IT systems for data entry.

Qualifications

• Associates Degree in a scientific discipline, engineering, or related field.
• 2+ years in GMP pharmaceutical manufacturing, R&D, or equipment manufacturing.
• Experience with batch records, QA operations, and line clearance in GMP environments.
• Hands-on experience as a manufacturing operator or packaging technician in regulated settings.
• Strong knowledge of cGMP and its daily application.

Responsibilities

• Train and follow all policies, SOPs, and regulatory requirements.
• Perform pharmaceutical manufacturing activities in a GMP environment with quality and safety standards.
• Execute batch records and maintain GDP, ensuring data is accurate and legible.
• Set up lines, perform changeovers, and operate production equipment per procedures.
• Conduct equipment setup, operation, cleaning, and ensure cleanliness and readiness.
• Use PPE and controls to perform tasks safely per safety policies.
• Conduct in-process inspections and sampling, document results as required.
• Enter data using IT platforms and electronic systems to support manufacturing and quality.
• Support developmental manufacturing experiments and document outcomes.
• Assist with deviations, corrective actions, and continuous improvement initiatives.
• Aid maintenance with preventative maintenance and basic troubleshooting.
• Contribute to continuous improvement and stay current with industry trends.

Skills

GMP experience

Documentation

Equipment operation

SOPs & GDP

Quality compliance

Process improvement

Education

Associate degree in a scientific discipline

Job description

Actalent in New Jersey seeks a Manufacturing Operator to join a fast-paced pharmaceutical operation. You will operate manufacturing equipment, document processes meticulously, and collaborate with quality, maintenance, and development teams to produce clinical supplies and support development experiments.

Responsibilities include following SOPs and GDP, setting up lines, performing changeovers, conducting in-process inspections, and using IT systems for data entry.