48 Quality Assurance Departments jobs in Bradford

Title: QC Assistant
Location: West Yorkshire
Salary: 28,000-30,000
Term: Permanent

SRG is working with an independent contract manufacturer of personal care / skincare products, based in West Yorkshire. They are now looking for a quality control assistant to join the team. You would be responsible for wet chemistry / bench chemistry testing and techniques. Ensure products meet specifications, as well as some small-scale formulation projects. This position would be an excellent opportunity for someone with experience in Quality Control or lab-based testing to join a supportive, friendly, family-owned company.

Working Hours: Monday to Friday 7:30am to 4:15pm (Mon-Fri), 45-minute lunch break

Role / Description

• QC testing of raw materials, in-process samples and finished product to check batches meet specifications
• Development and implementation of SOP's and QC procedures
• Lab techniques include PH testing, viscosity, stability testing and packaging compatibility testing
• Conduct routine microbiological and physical testing on products to ensure batches are compliant against industry regulations
• Work in harmony with Production and QA to achieve production delivery plans and resolve any quality issues
• Collaborate with stakeholders to ensure R&D, production and packaging compliance and resolve any inconsistencies to ensure batch consistency
• Formulation and development of batches to help improve new and existing batches

Requirements

• 2+ years recent experience in QC testing / wet chemistry within the personal care / skincare industry
• Willing and able to work stood up in a Fast-paced manufacturing environment
• Experience of working to cosmetic regulations such as EU Cosmetics Regulation, UK REACH, FDA etc.
• Strong communication skills and can relay information accurately
• Full right to work in the UK - there is no sponsorship available for this role

SRG is the UK's number one recruitment company specialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV For more information regarding this position or any others, please call Rhi on (phone number removed).

If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit (url removed) to view our other vacancies.

Keywords: formulation, NPD, new product development, new product innovation, packaging development, sustainable packaging, packaging trends, packaging innovation, supplier management, green chemistry, beauty, cosmetics, skincare, personal care, haircare, packaging innovation, soap, quality, quality control, quality assurance, sop's, haccap, ISO22716, Six Sigma, EU Cosmetics Regulation, UK REACH, FDA, manufacturing, ingredient safety

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

• Perform quantitative and qualitative analyses of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, KF).
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Operate, calibrate, and maintain laboratory equipment, troubleshooting issues as they arise.
• Review and approve analytical data, ensuring accuracy and compliance with specifications.
• Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
• Maintain accurate and comprehensive laboratory records, including test results, instrument logs, and deviations.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements.
• Contribute to internal and external audits by providing documentation and expertise.
• Assist in the training and mentoring of junior laboratory personnel.
• Stay updated on new analytical technologies and regulatory changes impacting quality control.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
• Significant experience as a Quality Control Analyst in the pharmaceutical industry.
• Proficiency with a range of analytical instruments (HPLC, GC, etc.) and associated software.
• Thorough understanding of GMP regulations and quality management systems.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong attention to detail and accuracy.
• Effective written and verbal communication skills.
• Ability to work independently and collaboratively in a fast-paced laboratory environment.
• Experience with method validation and OOS investigations is highly desirable.

• Perform a range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titration).
• Prepare reagents, solutions, and standards accurately for testing.
• Interpret analytical data, document results meticulously, and compare them against established specifications.
• Identify and investigate any out-of-specification (OOS) results or deviations from standard procedures.
• Maintain laboratory equipment, ensuring proper calibration and functioning.
• Adhere strictly to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and all relevant safety regulations.
• Contribute to the validation and qualification of analytical methods and equipment.
• Write and review standard operating procedures (SOPs) and technical reports.
• Participate in internal audits and support external regulatory inspections.
• Collaborate effectively with production, R&D, and other departments to resolve quality-related issues.

• Bachelor's degree in Chemistry, Pharmaceutical Science, Biotechnology, or a related scientific discipline.
• Proven experience (2+ years) in a Quality Control laboratory environment, preferably within the pharmaceutical or biopharmaceutical industry.
• Strong practical knowledge of analytical instrumentation and techniques commonly used in pharmaceutical QC.
• Familiarity with GMP, regulatory guidelines (e.g., FDA, MHRA), and quality management systems.
• Excellent data recording and documentation skills.
• Strong problem-solving abilities and attention to detail.
• Ability to work independently and as part of a team in a fast-paced laboratory setting.
• Good written and verbal communication skills.
• Proficiency in using laboratory software and Microsoft Office Suite.

• Perform analytical testing on pharmaceutical raw materials, intermediates, and finished products.
• Operate, calibrate, and maintain analytical laboratory equipment (HPLC, GC, UV-Vis, etc.).
• Prepare reagents, solutions, and samples for analysis according to standard operating procedures.
• Document all laboratory activities and results accurately and in compliance with GLP/GMP.
• Review and interpret analytical data, identifying any deviations or out-of-specification results.
• Participate in the investigation of OOS results and assist in developing CAPAs.
• Contribute to method development and validation activities.
• Ensure laboratory compliance with regulatory standards and company policies.
• Maintain a clean, organized, and safe laboratory environment.
• Assist in the training and mentoring of junior laboratory personnel.

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific discipline.
• Significant hands-on experience in a pharmaceutical QC laboratory.
• Proficiency with analytical instrumentation and techniques (HPLC, GC, FTIR, UV-Vis, Dissolution).
• Knowledge of pharmacopoeias (USP, EP, BP) and GMP/GLP guidelines.
• Experience with method validation and OOS investigations is a strong advantage.
• Excellent documentation, data interpretation, and report writing skills.
• Strong organizational and time management abilities.
• Ability to work independently and collaboratively in a hybrid environment.

• Performing analytical testing on raw materials, in-process samples, and finished pharmaceutical products.
• Utilising various analytical techniques and instrumentation, such as HPLC, GC, spectroscopy, and wet chemistry.
• Interpreting test results, documenting findings, and preparing analytical reports.
• Ensuring all laboratory activities comply with GMP, FDA, and other relevant regulatory standards.
• Maintaining laboratory equipment and ensuring its calibration and functionality.
• Investigating out-of-specification (OOS) results and identifying root causes.
• Collaborating with other departments, including R&D and manufacturing, to resolve quality issues.
  This is a critical role within the pharmaceutical industry, demanding precision and a deep understanding of scientific principles. As a remote-focused position, it offers flexibility while requiring strict adherence to procedures and deadlines. We are looking for an analytical thinker with excellent problem-solving skills and a commitment to maintaining the highest standards of quality. If you are a motivated scientist with experience in pharmaceutical quality control and are seeking a remote opportunity that offers significant impact, we encourage you to apply. Your expertise will be highly valued.
  Qualifications:
  
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
  • Proven experience as a Quality Control Analyst in the pharmaceutical industry.
  • Strong knowledge of analytical techniques (e.g., HPLC, GC, UV-Vis, IR spectroscopy).
  • Familiarity with GMP, ICH guidelines, and regulatory requirements.
  • Excellent laboratory data analysis and interpretation skills.
  • Proficiency in using laboratory information management systems (LIMS) and standard software.
  • Strong written and verbal communication skills.
  • Ability to work independently and manage workload effectively in a remote setting.
    

• Develop and implement quality control plans and procedures.
• Monitor manufacturing processes to ensure compliance with quality standards.
• Analyze production data, identify defects, and determine root causes.
• Implement corrective and preventive actions (CAPA).
• Conduct internal quality audits and assessments.
• Manage supplier quality and incoming material inspections.
• Utilize statistical process control (SPC) techniques.
• Prepare quality reports and document findings.
• Collaborate with production and engineering teams on quality initiatives.
• Ensure adherence to relevant quality management systems (e.g., ISO 9001).

• Bachelor's degree in Engineering (Mechanical, Manufacturing, or related) or equivalent experience.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
• Strong knowledge of quality management systems (ISO 9001) and methodologies (SPC, Six Sigma, Lean).
• Proficiency in data analysis and interpretation.
• Excellent problem-solving and analytical skills.
• Strong written and verbal communication skills.
• Ability to work independently and manage time effectively in a remote setting.
• Experience with quality control tools and software.