SonicJobs Logo
Left arrow iconBack to search

QC Analyst - Level 1

SRG
Posted 2 days ago, valid for 17 days
Location

Ware, Hertfordshire SG11 1AY

Contract type

Part Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

info
  • The job title is QC Analyst Level 1 - Synergy located in Ware, UK, offering a salary of £27,000 - £28,000 per annum on a 12-month fixed-term contract.
  • The position is suitable for chemistry graduates or those with experience in an industrial chemistry lab looking to enhance their skills in a GMP environment.
  • Responsibilities include performing analysis of samples, preparing and checking analytical data, and assessing the quality and accuracy of results.
  • Candidates should have a relevant science degree and experience in QC testing of oral solid dose medicines, particularly with HPLC and other analytical techniques.
  • Proficiency in laboratory instruments and problem-solving is required, while GMP experience is desirable but not essential.

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.Q

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

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.