Junior QA Officer (Double Days shift)

Work Schedule

Environmental Conditions

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 youre part of Thermo Fisher Scientific youll 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 Fishers 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 100000 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 70000 extraordinary minds has a unique story to tell. Join us and contribute to our singular missionenabling our customers to make the world healthier cleaner and safer.