Junior QA Officer (Double Days shift)

Work Schedule

Rotational M-F days

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, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse

Job Description

Working hours: Double day shift pattern, Rotating Weekly, Monday to Friday (1 week of early shift, followed by 1 week of late shifts)

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.

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:

The Junior QA Officer will provide support to the Quality Operations team at Swindon site manufacturing facilities and support functions. You will assist the team by preparing and scanning GMP documents to clients to meet on-time delivery targets, completing independent verification of the visual inspection of sterile products (note that this requires successful completion of company vision test), and performing review of GMP documents to ensure compliance with procedures.

Responsibilities:

• Preparation and scanning of GMP documents

• Archiving of GMP documents

• Independent verification of visual inspection process

• Pass company eyesight test

• Completing documents in a GMP manner

• Review of GMP documents and identification or errors

• Ensure all training is completed on time

• 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.

What Experience / Qualifications are we looking for?

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

• Knowledge & understanding of cGMP

• Good understanding of Microsoft and Windows applications

• Excellent interpersonal skills with the ability to work to strict timelines

• Good organizational and time management skills.

Benefits we offer:

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 70,000 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.