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QC Analyst - Level 1

QC Analyst - Level 1

SRG

Posted 9 days ago, valid for 11 days

Ware, Hertfordshire SG11 1AY

£24,000 - £28,800 per annum

Part Time

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Sonic Summary

The position is for a QC Analyst Level 1 at a pharmaceutical organization in Ware, UK, offering a salary between £27,000 and £28,000 per annum on a 12-month fixed-term contract.
Candidates should ideally be chemistry graduates or have a background in an industrial chemistry lab, with an interest in developing skills in a GMP environment.
Key responsibilities include performing analyses of samples, preparing and checking analytical data, and assessing the quality of results to ensure compliance with acceptance criteria.
Applicants are required to have a relevant science degree and experience in QC testing of oral solid dose medicines, particularly with HPLC and other analytical techniques.
While GMP experience is desirable, it is not essential, and the role provides opportunities for training and development within the company.

Job Title: QC Analyst Level 1 - Synergy

Location: Ware, UK

Salary: £27,000 - 28,000 p/a

contract: 12 month FTC

Are you a chemistry graduate looking for your first role in industry? Or do you already have a background in an industrial chemistry lab but would like to develop your skills further in a GMP environment?

SRG Synergy are currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a QC Analyst - Level 1

Synergy, part of SRG, offer a range of scientific solutions to different Clients in the Life Sciences sector. We can offer a competitive salary, a range of excellent benefits and access to training & development opportunities within the role.

Responsibilities:

Performs analysis of samples and supports technical investigations/ monitoring, using a range of analytical techniques related to the testing of oral solid dose medicines including HPLC for assay and impurities, dissolution, homogeneity, content of uniformity, pharmacopoeia and physical property tests
Prepares and checks analytical data accurately according to company, customer and regulatory requirements
Assesses the quality and accuracy of analytical results and determines if material meets pre-defined acceptance criteria
Undertakes analysis as required to support process investigations or as part of process qualification and validation exercises.
Is responsible for assigned items of Laboratory equipment or 5S standards.
Responsible for the safety of self and others within the Laboratory

Requirements:

Relevant Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) or equivalent.
Experienced in QC testing of oral solid dose medicines including HPLC for assay and impurities, dissolution, homogeneity, content of uniformity, pharmacopoeia and physical property tests.
Is proficient in the use of numerous Laboratory instruments, software packages and other analytical techniques (e.g. Empower 3).
Is proficient in problem solving and may have expertise in troubleshooting analytical equipment.
GMP experience would be desirable but not essential.

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

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