QC Technician (Inspection & Packaging) - [2 positions available]

Work Schedule

Other

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, Fluctuating Temps hot/cold, Laboratory Setting, No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Warehouse, Will work with hazardous/toxic materials

Job Description

Shift Pattern: 24/7 - 2 shifts on, 2 days off, 3 shifts on, 2 days off, 2 shifts on, 3 days off, etc.. Shifts will rotate between Day shift, 6.45am to 7pm, and Night shifts 6.45pm to 7am.

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 $40 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!

Location/Division Specific Information:

Thermo Fisher’s Swindon facility specializes in integrated sterile liquid and lyophilized product development and commercial manufacturing, including high potency products and LVP. The Swindon facility offers extensive development and commercial capabilities for sterile dosage forms, including liquid vials, commercial fill finish lines, primary and secondary packaging vials.

Position Summary:

This role will provide support for the Quality Control team at Swindon site manufacturing facilities and support functions. You will assist the team by completing independent verification of the visual inspection of sterile products (note that this requires successful completion of company vision test), performing QC analysis of packaging materials and engineering components to support manufacture and release of pharmaceutical products and completing the associated documentation in accordance with cGMP and ALCOA+ principles.

Responsibilities:

• Independent verification of visual inspection process

• Pass company eyesight test

• Completing documents in a GMP manner

• Understand emergency procedures and follow safe systems of work.

• Ensure compliance with environment, health and safety and security policies and procedures, rules, signage and instructions at all times

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

• Perform quality control analytical testing of incoming goods, packaging materials and engineering components to ensure compliance with QC Specifications.

• Perform planned preventative maintenance and performance calibrations on equipment 

• Maintain own training records and support and train other team members as required

• Participate in continuous improvement activities and look for further opportunities to progress the team/department

• Communicate optimally with others on site and internationally, and to participate with them in problem solving activities 

• Ensure cGMP is applied in their area of work and align with cGMP in all areas of the business 

• Work with HSE, cGMP and 5S in mind at all times

• Carry out any other tasks which may be required from time to time 

• Ensure compliance with environment, health and safety and security policies and procedures, rules, signage and instructions at all times 

Requirements:

Education:

• High School Diploma, Secondary Education, Advanced Certificate, or equivalent

What Experience / Qualifications are we looking for?

• Experience working within a GMP environment, preferably in the pharmaceutical industry

• Knowledge & understanding of cGMP

• Ability to meet vision test requirement (with or without glasses) 

• Ability to differentiate between colours

• Good understanding of Microsoft and Windows applications

• Good organizational, time management skills and attention to detail

• Ability to follow written instructions consistently

• Experience working under tight deadlines while maintaining accuracy

• Proficient in basic mathematics and literacy

• Effective communication skills at all internal and external levels

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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.