Quality Control Analyst

Glasgow, Scotland SRG

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Job Description

Exciting QC Analyst III Opportunity in Glasgow


Are you a talented Quality Control Analyst looking to join a dynamic and growing company? This could be the perfect opportunity for you!


We are working on a role for a very experienced QC Analyst from the pharmaceutical industry to play a key role in the QC team.

If you are currently an experience Analyst or Senior, then this could be the job for you.


The Role

The QC Analyst is a crucial member of the team, responsible for ensuring that the company's products meet the highest quality standards. As a QC Analyst, you will be involved in a variety of tasks, including:


  • Conducting testing on in-process, finished product, and raw materials using a range of analytical techniques including but not limited to HPLC analysis, UV, IR, GC, and particle size analysis, in accordance with the relevant procedures and cGMP
  • Reviewing data and documentation as required in line with regulatory requirements
  • Liaising with production supervisors to schedule and report on in-process testing
  • Documenting test results and interpreting data to identify any out-of-specification or out-of-trend results
  • Assisting with laboratory investigations and implementing corrective and preventive actions
  • Maintaining a clean and organized working environment within the Quality Control Laboratory


What We're Looking For

To be successful in this role, you will need:


  • A degree in chemistry or a related field
  • Previous experience working in a similar quality control laboratory environment
  • Strong troubleshooting and method development skills, particularly with HPLC
  • Experience in with complex HPLC (UV-VIS, CAD, IC) analysis/validation essential
  • Knowledge of regulatory requirements such as GLP and GMP
  • Excellent attention to detail and the ability to work to tight deadlines
  • A customer-focused attitude and the ability to collaborate effectively with colleagues
  • Ability to work in a fast-paced and changing environment


Why Join This Company?

This company offers a positive and supportive work environment, with plenty of opportunities for learning and development. You'll be part of a talented team that is committed to excellence and making a real difference in the pharmaceutical and biotechnology industries.


If you're excited about the prospect of joining the QC Analyst team, we'd love to hear from you. Apply now and take the first step towards an rewarding and fulfilling career!

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Senior Quality Control Inspector

G1 1TT Glasgow, Scotland £30000 Annually WhatJobs

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full-time
Our client, a leading manufacturing firm renowned for its high-quality products, is seeking a meticulous and experienced Senior Quality Control Inspector to join their team in **Glasgow, Scotland, UK**. This role is critical in ensuring that all manufactured goods meet stringent quality standards and customer specifications. You will be responsible for conducting inspections, identifying defects, implementing corrective actions, and contributing to the continuous improvement of quality processes. The ideal candidate will have a keen eye for detail, a strong understanding of quality management systems, and a commitment to excellence.

Key Responsibilities:
  • Perform comprehensive quality inspections on raw materials, in-process components, and finished products using various measuring instruments and testing equipment.
  • Interpret technical drawings, specifications, and quality standards to ensure compliance.
  • Identify, document, and report non-conforming products and initiate corrective action procedures.
  • Collaborate with production and engineering teams to resolve quality issues and implement preventive measures.
  • Conduct root cause analysis for quality defects and recommend process improvements.
  • Maintain accurate records of inspection results, test data, and quality reports.
  • Participate in internal and external audits related to quality management systems (e.g., ISO 9001).
  • Train and mentor junior quality control personnel.
  • Ensure proper calibration and maintenance of all inspection and testing equipment.
  • Monitor production processes to identify potential quality risks.
  • Assist in the development and implementation of quality control procedures and work instructions.
  • Contribute to supplier quality assurance activities.
  • Review and approve production documentation for quality compliance.
  • Uphold company standards for safety and workplace organization.
  • Promote a quality-first culture throughout the manufacturing facility.

Qualifications:
  • High school diploma or equivalent; technical certification or associate’s degree in a related field preferred.
  • Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
  • Proven experience with various inspection techniques and measurement tools (e.g., calipers, micrometers, gauges, CMM).
  • Strong understanding of quality management systems (e.g., ISO 9001) and statistical process control (SPC).
  • Ability to read and interpret technical drawings, blueprints, and specifications.
  • Excellent attention to detail and accuracy.
  • Strong analytical and problem-solving skills.
  • Good communication and teamwork abilities.
  • Proficiency in using quality control software and databases.
  • Experience in a specific manufacturing sector (e.g., automotive, aerospace, electronics) is a plus.
  • Ability to work independently and as part of a team.
  • Knowledge of Lean Manufacturing principles is beneficial.

This role offers a competitive salary, benefits, and the opportunity to be part of a respected manufacturing team.
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Remote Pharmaceutical Quality Control Analyst

G1 2DU Glasgow, Scotland £35000 Annually WhatJobs

Posted 4 days ago

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full-time
Our client, a leading pharmaceutical company, is seeking a meticulous and highly motivated Pharmaceutical Quality Control Analyst to join their innovative, fully remote team. This role is critical in ensuring the quality and safety of pharmaceutical products by conducting rigorous laboratory analyses and adhering to strict regulatory guidelines. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products using established methodologies and state-of-the-art equipment. Your duties will include preparing samples, operating analytical instruments such as HPLC, GC, and UV-Vis spectrophotometers, interpreting test results, and documenting all activities accurately in compliance with GMP (Good Manufacturing Practice) standards. The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline, coupled with proven experience in pharmaceutical quality control or analytical testing. Hands-on experience with common analytical techniques and laboratory equipment is essential. Strong understanding of regulatory requirements within the pharmaceutical industry, including ICH guidelines and pharmacopoeial standards (e.g., USP, EP), is highly desirable. You must demonstrate exceptional attention to detail, excellent data analysis and problem-solving skills, and the ability to work independently and manage your time effectively in a remote setting. Excellent written and verbal communication skills are necessary for preparing reports and collaborating with cross-functional teams. This is a fantastic opportunity to contribute to the development and manufacturing of life-saving medicines from the comfort of your own home office, working with a supportive and expert team. If you are passionate about quality assurance in the pharmaceutical sector and seeking a challenging remote role, we encourage you to apply.
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