Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Working shift pattern: 24/7 - rotating day and night shift

When you’re part of Thermo Fisher Scientific, you’ll do challenging work and be part of a team that values performance, quality, and innovation. As part of a successful, growing global organization, you will be encouraged to perform at your best. With revenues of $20 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

Responsibilities:

• Set up and operation of the Automatic visual inspection & packing lines in accordance with Standard Operating Procedures (SOPs)

• Perform AVI and packing of pharmaceutical products (Sterile & non-sterile) in accordance with Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs)

• Perform AVI and Packaging operational duties, e.g., line clearance, In Process Checks (IPC) checks, replace components on line, complete batch & associated documentation, right first time for accordance with SOPs to ensure compliance with cGMP

• Set equipment to ensure minimum downtime levels, minimum product damage/waste, support machine start-up, changeovers, testing, and cleaning activities in accordance with SOP's and cGMP requirements

• Monitoring equipment status and readiness for inspection & packing, reporting any faults or issues to Supervision

•  Cleaning and maintenance of clean rooms/equipment to SOPs, cGMP, and pharmaceutical industry regulatory standards

• To ensure any instances of non-conformance are communicated to the Process Coordinator, Area Manager, or Quality Assurance representatives to ensure that they are investigated and rectified

• Support project validation work and new product introduction to the Operations department

• Using Quality systems for GMP changes and report writing.

• Conduct and assist, where appropriate, in basic equipment maintenance

GMP:

• Ensure products are inspected and packed, and documentation is completed in accordance with GMP and Standard Operating Procedures.

• Support the Process Coordinator in performing Level 1 audits.

• Support relevant Deviation and Complaint investigations and determination of appropriate CAPA as required.

• Maintain a high level of tidiness and cleanliness at all times – personal, work area, and department.

• Take ownership, accountability, and enforce good GMP and GDP within the GMP facility.

EH&S:

• Understand emergency procedures and comply with safe systems of work.

• Ensure compliance with environmental, health, and safety rules, signage, and instructions at all times.

• Ensure prompt reporting and investigation of all accidents, near misses, and breaches of rules.

Qualifications/Experience:

• Experience in clean room working, knowledge of AVI, packaging, and serialization is highly desirable 

• Strong competency in English and Maths is essential, and a scientific background is essential (e.g. A-Levels)

• Excellent communication and teamwork skills, with the ability to manage your own workload

• Understanding of HMI-driven pharmaceutical systems

At Thermo Fisher Scientific, each one of our 120,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner, and safer.