Pharmaceutical & Biotechnology
Tablet Inspection Operator
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Contract
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North Dublin, County Dublin, Ireland
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42045066
PE Global is currently recruiting for a Tablet Inspection Operator for a leading multi-national Pharmaceutical client based in North Dublin.
This is an initial 6-month contract working a 24/5 shift pattern:
3 cycle shift rotation
Week 1: Day shift – 06:30 – 18:30 Monday and Tuesday off Wednesday back in Night shift 18:30 – 06:30 Thursday and Friday (4-day week)
Week 2: Day shift – 06:30 – 18:30 Wednesday, Thursday, Friday (3-day week)
Week 3: Night shift – 18:30 – 06:30 Monday, Tuesday, Wednesday (3-day week)
Position Summary:
The Tablet Inspection Operator performs functions related to the visual inspection of drug products. The position incumbent is expected to adhere to all cGMP compliance and regulatory mandates and quality requirements and comply with all SOPs and internal policies and procedures in the performance of job duties.
The Tablet Inspection Operator correctly follows SOPs to complete tasks and applies skills and knowledge to recognize issues that impact production efficiency, throughput, quality, and/or the fulfilment of the assigned production targets.
The Tablet Inspection Operator is responsible for the safe, compliant, and efficient execution of job duties in a team environment.
The role may also require working in Class C cleanroom environment.
Responsibilities:
- Actively highlight any safety concerns to assist in the reduction of accidents or near misses.
- Support and adhere to established manufacturing scheduling processes and production targets.
- Handle raw materials and/or intermediate or finished products according to applicable SOPs.
- Gowning correctly and wearing of assigned PPE,
- Perform AQL sampling.
- Complete all required production data entries and calculations for manufactured batches on the BMR/EBR worksheets/SIC logs with detail and accuracy in real time.
- Observe established escalation process for issues impacting established production-related Service Level Agreements (SLAs) and/or fulfilment of production goals.
- Recognize and report to immediate supervisor any process or equipment anomalies and/or deviations from accepted standards.
- Provide status updates on manufacturing activities and operational challenges according to defined procedures.
- Perform master cleans and surface cleans of manufacturing equipment and production areas according to established SOPs and SLAs.
- Execute changeovers between batches according to established SOPs and SLAs.
- Keep work area neat and orderly and observe all safety and compliance procedures.
- Seek process innovation and continuous process improvement in production area.
- Complete and conform to all training requirements for job role, including company-required and machine-specific training.
- Carry out and assist in the ongoing training of new and existing personal as required in the area of manufacture.
- Can work equally well in a large or small team environment, where communication and feedback between team members and across shifts is critical.
- May participate in department initiatives and projects.
Requirements:
- Secondary School Leaving Cert, or equivalent
- Exposure to pharmaceutical manufacturing equipment or equivalent
- Basic Microsoft Excel and Word skills
- EBR and TrackWise knowledge desirable
- May need to undergo a yearly test for 20/20 vision and colourblindness
Interested candidates should submit an updated CV.
Please click the link below to apply, alternatively send an up-to-date CV to sean.molloy@peglobal.net
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland****
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