Work Schedule
12 hr shift/nightsEnvironmental Conditions
Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Loud Noises (Equipment/Machinery) Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Strong Odors (chemical lubricants biological products etc.) Various outside weather conditions Will work with hazardous/toxic materialsJob Description
Working shift: 4 days on / 4 days off - Night shift (6pm to 6am)
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
How Will You Make an Impact:
The QC Technician role at Thermo Fisher Scientific (Cramlington) ensures raw materials in-process items and finished products meet strict quality standards before they reach customers. Carrying out environmental monitoring in the ISO 7 cleanroom helps prevent contamination maintain compliance and protect production continuity. Ultimately the job safeguards product reliability and supports the companys mission to enable healthcare scientific research and patient safety.
What you will do:
Perform QC testing in accordance with approved procedures e.g. Bioburden Endotoxin and Tensile testing.
Conduct environmental monitoring of the cleanroom areas.
Perform testing and release of raw materials within a warehouse environment and Cleanroom sampling area.
Generate final product Certificates of Analysis in accordance with the approved product specification.
Support the non conforming process and disposal of expired and reject materials.
Ensure consumable stock of QC materials is maintained.
Complete QC records and maintain QC databases.
Participate in quality investigations.
Manage assigned responsibilities within the Quality Management System and Documentation System.
Support the continuous improvement program to drive quality safety and process improvements.
Candidate Requirements:
Education: (EMEA)
Science related GCSEs or equivalent
Experience:
Required: Minimum of 2 years of work experience in QA or QC or related field
Preferred: Experience in a cGMP environment
Knowledge Skills Abilities:
Excellent written and oral communication skills
Meticulous attention to detail
Excellent team work and problem solving skills
Ability to manage priorities and work to set timeframes
Excellent IT skills
Willingness to learn and drive process improvements
Physical Requirements / Work Environment
Work Environment
Cleanroom
Warehouse
Laboratory
Office
Physical Requirements:
Ability to stand and/or walk for extended periods and perform physical activities including bending reaching and lifting up to 2550 lbs.
Manual dexterity and visual acuity required to operate testing equipment perform detailed inspections and accurately read gauges instruments and documentation.
Ability to work safely in an environment with exposure to noise temperature variations chemicals and moving machinery while wearing required personal protective equipment (PPE).
Required Experience:
IC
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