Work Schedule
Rotational M-F daysEnvironmental 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.) WarehouseJob 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.
Required Experience:
Junior IC
Junior QA Officer (Double Days shift) • Swindon, England, UK
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