Pharma Production Operator - GMP & Quality Focus

Occupli Limited; Cork; Hybrid; EUR 30,000 - 38,000; Full time

Job summary

Occupli Limited invites applications for a Production Operator role at our Cork operation, within a highly regulated pharmaceutical manufacturing environment. The role emphasizes quality, safety, compliance, and meticulous documentation to support daily manufacturing activities.

The successful candidate will join an established production team, executing procedures, completing records in real time, and upholding GMP standards across production areas.

Qualifications

• Experience in pharmaceutical, life sciences, or other regulated manufacturing environments.

Responsibilities

• Support day-to-day production activities in line with procedures.
• Monitor production processes and perform in-process checks.
• Complete production records and batch documentation in real time.
• Carry out routine quality and process checks.
• Support sampling and liaise with Quality teams.
• Identify and report deviations or quality concerns.
• Maintain GMP, hygiene and housekeeping standards.
• Clean production equipment and areas.
• Ensure materials are identified, handled and stored properly.
• Follow safety procedures and environmental requirements.
• Use PPE and safety equipment as required.
• Support investigations and continuous improvement initiatives.
• Collaborate with Production, Quality, Engineering and other functions.
• Support Right First Time culture through accurate execution.

Skills

Pharma manufacturing experience

GMP knowledge

Documentation proficiency

Attention to detail

Quality awareness

Communication skills

Fluent English

SAP familiarity

Education

Pharmaceutical manufacturing qualification

Science/Engineering background

Tools

SAP

Job description

Occupli Limited invites applications for a Production Operator role at our Cork operation, within a highly regulated pharmaceutical manufacturing environment. The role emphasizes quality, safety, compliance, and meticulous documentation to support daily manufacturing activities.

The successful candidate will join an established production team, executing procedures, completing records in real time, and upholding GMP standards across production areas.