QC Analyst

Dyddiad hysbysebu:	30 Medi 2025
Cyflog:	£27,000 bob blwyddyn
Oriau:	Llawn Amser
Dyddiad cau:	14 Hydref 2025
Lleoliad:	Kingston Upon Hull, East Riding of Yorkshire, HU8 7DS
Gweithio o bell:	Ar y safle yn unig
Cwmni:	Carbon60
Math o swydd:	Cytundeb
Cyfeirnod swydd:	BBBH168184_1759226889

Crynodeb

Quality Control Analyst

ROLE SUMMARY: Synergy is a Scientific Services provider with customers across the life sciences. Our team at Reckitt provide stability analysis and Quality Control services to a portfolio of health and well-being products and projects. We are seeking highly motivated individuals with previous experience of instrumental methods and a hands-on approach to their own development, to expand our team and range of activities. The role is available for 12 months in the first instance with potential for extension. Working closely with R&D, the role will focus mainly on the generation, analysis, and reporting of analytical data in line with GMP/GLP standards, using techniques including HPLC, GC, and a variety of other instrumental and wet chemistry techniques. You will also have opportunity to be involved in stability studies, method development, validation and transfer and QC/QA processes such as deviations, lab investigations, CAPA and audit support. Synergy has a strong focus on learning and development, and you will undergo extensive training, both in technical aspects of the role and in areas such as GMP and Continuous Improvement.

PRINCIPAL ACCOUNTABILITIES: Perform sample and batch assays using HPLC and other instrumentation, following established protocols Order, receive, prepare and label samples in accordance with SOPs Analyse, report, and record trends of results Contribute to protocol development for QC and stability trials Identify and escalate any out of specification / out of trend / unexpected results Proactively identify issues and appropriate actions to address Ensure compliance with all relevant Health and Safety systems and legislation Execute tasks according to regulatory, statutory, or client defined standards and requirements Comply with all appropriate Synergy and Client defined Quality Management Systems, processes, and procedures, including the timely capture and recording of laboratory data Contribute to continuous improvement activities with respect to compliance, H&S, and audit readiness Meet / exceed the defined project KPI's & individual objectives Actively participate in Synergy training and performance review processes Develop and maintain excellent customer relationships, always ensuring that you act in a professional manner whilst performing your duties or whilst you are representing Synergy any capacity Other duties as reasonably requested by the Synergy Team Leader

KEY WORKING RELATIONSHIPS: Synergy Team Leader and team members Synergy Operations Manager Client laboratory leaders, R&D teams and other lab users

QUALIFICATIONS AND EXPERIENCE: · Degree in a relevant scientific discipline such as Chemistry, Pharmaceutical or Biological Science, or equivalent professional experience · Previous hands-on experience of analytical test methods such as HPLC within a Healthcare / FMCG / Medical Device environment is desirable · Results orientated, self-motivated with an ability to evaluate and manage risks · Excellent communication skills, including presentation skills and relationship building · Ability to work efficiently without compromising quality and delivery

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.