Quality Control Microbiologist

Perth, Scotland Stem Recruitment

Posted 1 day ago

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Job Description

contract

STEM Recruitment Solutions is seeking a Senior Quality Control Technician/ Microbiologist for our client based in Perthshire, Scotland.

This will initially be a 6 month contract with the potential to go permanent for the right candidate and if business needs allow. The main job responsibilities of the candidate will be:

  • Collect and process samples ready for testing.
  • Perform pH testing and microbiological testing of samples.
  • Microbiological testing in strict accordance with the ISO 17025 & 13485/9001 Quality Management Systems and Quality Policies.
  • Report non-conforming results to the QC Team Leader or Quality Manager meticulously.
  • In-depth knowledge of ISO 17025 testing procedures.
  • Proficiency in aseptic technique and fundamental pipetting techniques.
  • Experience with contamination checks, pH, conductivity, membrane filtration, and media fertility testing.

The ideal candidate will have as a minimum a BSc in Microbiology or other related field, or equivalent experience. Demonstrated experience working in a laboratory environment is advantageous but the position would also suit a recent graduate with the relevant skills.

Our client offers competitive contract rates, a supportive work environment, and opportunities for professional development within the biotechnology sector. This role is ideal for candidates eager to utilise their microbiology expertise in a vital QC function, contributing to innovative research and product quality assurance.

As this is a short term contract role preference will be given to candidates readily available to commute to site.

Please apply online in the first instance or for more information contract Alex at STEM.

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Senior Pharmaceutical Quality Control Analyst

EH6 5JQ Edinburgh, Scotland £55000 Annually WhatJobs

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full-time
We are seeking a highly skilled and experienced Senior Pharmaceutical Quality Control Analyst to join our dedicated, fully remote team. This critical role will involve ensuring the quality and integrity of our pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and state-of-the-art equipment. As a senior member of the QC department, you will contribute to method development, validation, and transfer activities, ensuring adherence to regulatory guidelines such as GMP (Good Manufacturing Practice) and ICH. Your responsibilities will include detailed data analysis, interpretation of results, and accurate documentation in compliance with pharmacopoeial standards and internal SOPs. You will also play a key role in troubleshooting analytical issues, investigating deviations, and implementing corrective and preventive actions (CAPAs). This position requires a thorough understanding of analytical chemistry, spectroscopy, chromatography (HPLC, GC), and other relevant pharmaceutical testing methodologies. The ideal candidate will possess excellent scientific judgment, strong problem-solving skills, and the ability to work independently with minimal supervision in a remote setting. Experience with LIMS (Laboratory Information Management System) is highly desirable. You will contribute to internal and external audits by preparing relevant documentation and participating in discussions. This role offers the opportunity to make a significant impact on product quality and patient safety while enjoying the flexibility of a remote-first work environment. Excellent communication skills are essential for effective collaboration with cross-functional teams, including R&D, manufacturing, and regulatory affairs. We are looking for a motivated individual with a passion for quality assurance in the pharmaceutical industry. Proficiency in data integrity principles and good documentation practices is paramount.

Responsibilities:
  • Perform analytical testing on pharmaceutical materials and products.
  • Conduct method development, validation, and transfer studies.
  • Analyze and interpret test results, ensuring data integrity.
  • Document all laboratory activities according to GMP and SOPs.
  • Troubleshoot analytical equipment and methods.
  • Investigate deviations and implement CAPAs.
  • Ensure compliance with pharmacopoeial and regulatory standards.
  • Contribute to audits and regulatory submissions.
  • Collaborate with cross-functional teams to resolve quality issues.
  • Maintain a safe and organized laboratory environment (virtually).
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