Laboratory Technical Support Specialist (M/F/D)
Apply locations Macclesfield, GBR time type Full time posted on Posted 2 Days Ago job requisition id R-161115 The Opportunity: Avantor is looking for a quality-driven
Technical Support Specialist
to join our Scientific Preparation team based in
Macclesfield, UK . In this position, you will take ownership of ensuring laboratory equipment meets GMP standards, prepared solutions align with our high-quality standards, and all documentation remains compliant throughout laboratory operations. This role will be a full-time permanent position based at our customer’s site in
Macclesfield (SK10 2NA) . Next to an attractive salary, we offer multiple benefits such as a bonus, pension scheme, private medical and dental care, and an additional day off for your birthday. Working hours:
Monday to Friday, 8:00 am – 4:00 pm (flexible) The team: You’ll be part of our highly skilled, close-knit
Laboratory Scientific Preparation Team , consisting of five associates. This team is responsible for preparing buffers, reagents, and solutions used across laboratories. You will be part of our Lab and Production Services department, which supports leading pharmaceutical companies and laboratories around the world, advancing research and development in the Life Sciences industry. What we’re looking for: Education:
A Bachelor’s degree in a scientific discipline or equivalent experience. Experience: A minimum of 2 years experience working in a laboratory environment, with at least 1 year in GxP-regulated laboratories. Expertise in the use of electronic laboratory notebook systems (e.g., ELab, 1Lab). Strong knowledge of GMP, SHE, and GDP requirements in a laboratory setting. Experience in writing, maintaining, and updating SOPs and Work Instructions. High proficiency in Word and Excel, with proven experience in data entry, analysis, and reporting. How you’ll thrive and create an impact: Take ownership of laboratory equipment, ensuring it meets GMP standards throughout its lifecycle. Lead investigations when deviations occur, identifying and implementing corrective actions. Oversee the ongoing upkeep of the 1Lab electronic notebook system, ensuring accurate and compliant data capture in line with GMP and GDP standards. Write, update, and maintain SOPs and work instructions to GMP standards, supporting compliance, service delivery, and training across the team. Support in root cause analysis of non-conformances and deviations, collaborating with the Quality Lead and Scientific Preparation team to implement effective corrective actions. Assist the Scientific Preparation Manager in preparing for both internal and external audits. Ensure that all documentation and processes comply with GMP. Why Avantor? Dare to go further in your career.
Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better.
It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world.
Apply today!
#J-18808-Ljbffr
Apply locations Macclesfield, GBR time type Full time posted on Posted 2 Days Ago job requisition id R-161115 The Opportunity: Avantor is looking for a quality-driven
Technical Support Specialist
to join our Scientific Preparation team based in
Macclesfield, UK . In this position, you will take ownership of ensuring laboratory equipment meets GMP standards, prepared solutions align with our high-quality standards, and all documentation remains compliant throughout laboratory operations. This role will be a full-time permanent position based at our customer’s site in
Macclesfield (SK10 2NA) . Next to an attractive salary, we offer multiple benefits such as a bonus, pension scheme, private medical and dental care, and an additional day off for your birthday. Working hours:
Monday to Friday, 8:00 am – 4:00 pm (flexible) The team: You’ll be part of our highly skilled, close-knit
Laboratory Scientific Preparation Team , consisting of five associates. This team is responsible for preparing buffers, reagents, and solutions used across laboratories. You will be part of our Lab and Production Services department, which supports leading pharmaceutical companies and laboratories around the world, advancing research and development in the Life Sciences industry. What we’re looking for: Education:
A Bachelor’s degree in a scientific discipline or equivalent experience. Experience: A minimum of 2 years experience working in a laboratory environment, with at least 1 year in GxP-regulated laboratories. Expertise in the use of electronic laboratory notebook systems (e.g., ELab, 1Lab). Strong knowledge of GMP, SHE, and GDP requirements in a laboratory setting. Experience in writing, maintaining, and updating SOPs and Work Instructions. High proficiency in Word and Excel, with proven experience in data entry, analysis, and reporting. How you’ll thrive and create an impact: Take ownership of laboratory equipment, ensuring it meets GMP standards throughout its lifecycle. Lead investigations when deviations occur, identifying and implementing corrective actions. Oversee the ongoing upkeep of the 1Lab electronic notebook system, ensuring accurate and compliant data capture in line with GMP and GDP standards. Write, update, and maintain SOPs and work instructions to GMP standards, supporting compliance, service delivery, and training across the team. Support in root cause analysis of non-conformances and deviations, collaborating with the Quality Lead and Scientific Preparation team to implement effective corrective actions. Assist the Scientific Preparation Manager in preparing for both internal and external audits. Ensure that all documentation and processes comply with GMP. Why Avantor? Dare to go further in your career.
Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better.
It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world.
Apply today!
#J-18808-Ljbffr
