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, 9:00am – 5:00pm 

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 laboratoriesExpertise in the use of electronic laboratory notebook systems (e.g., ELab, 1Lab)Strong knowledge of GMP, SHE and GDP requirements in a laboratory settingExperience in writing, maintaining, and updating SOPs and Work InstructionsHigh 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 standardsWrite, update, and maintain SOPs and work instructions to GMP standards, supporting compliance, service delivery, and training across the teamSupport in root cause analysis of non-conformances and deviations, collaborating with the Quality Lead and Scientific Preparation team to implement effective corrective actionsAssist the Scientific Preparation Manager in preparing for both internal and external audits. Ensure that all documentation and processes comply with GMP and maintain ISO 9001:2015 accreditation

#LI-Onsite 

Disclaimer:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

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!

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at recruiting@avantorsciences.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

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We will use the personal information that you have submitted to us in order to consider your application for the relevant role.
 

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3rd Party Non-Solicitation Policy:

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.