87 Quality Assurance Specialist jobs in London

• Reviewing and approving batch production and control records.
• Participating in internal and external audits and inspections.
• Managing and investigating deviations, out-of-specifications (OOS), and out-of-trend (OOT) results.
• Developing, implementing, and maintaining Corrective and Preventive Actions (CAPA).
• Ensuring compliance with current Good Manufacturing Practices (cGMP) and other relevant regulatory guidelines.
• Conducting risk assessments and developing mitigation strategies.
• Reviewing and approving validation protocols and reports.
• Participating in vendor qualification and management activities.
• Providing training on quality assurance principles and practices.
• Contributing to the continuous improvement of the QMS.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with GMP, ICH, and other relevant regulatory guidelines.
• Conduct internal and external audits of manufacturing sites, suppliers, and contract manufacturers.
• Review and approve batch records, validation protocols, and reports.
• Investigate deviations, out-of-specifications (OOS), and customer complaints, ensuring effective root cause analysis and CAPA implementation.
• Manage change control processes, assessing the impact of changes on product quality and regulatory compliance.
• Prepare and review regulatory submission documentation.
• Provide training and guidance to QA staff and other departments on quality principles and procedures.
• Participate in regulatory inspections and respond to queries from health authorities.
• Monitor key quality metrics and trends, and report on the effectiveness of the QMS.
• Ensure compliance with all applicable regulatory requirements throughout the product lifecycle.
• Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality and compliance.
• Support the development and implementation of new quality initiatives and continuous improvement programs.
• Review and approve Standard Operating Procedures (SOPs) and other quality-related documents.
• Maintain up-to-date knowledge of global pharmaceutical regulations and industry best practices.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• A minimum of 6 years of experience in Pharmaceutical Quality Assurance or Quality Control.
• In-depth knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and relevant regulatory guidelines (e.g., FDA, EMA, ICH).
• Experience with audits, change control, deviation management, and CAPA systems.
• Excellent understanding of pharmaceutical manufacturing processes and product development.
• Strong analytical and problem-solving skills.
• Exceptional attention to detail and accuracy.
• Proficient in using quality management software and standard office applications.
• Excellent written and verbal communication skills.
• Ability to work independently and manage multiple priorities effectively in a remote setting.

• Oversee and manage the Quality Management System (QMS).
• Review and approve critical documentation, including batch records, deviations, and change controls.
• Investigate product quality complaints and deviations, implementing corrective and preventive actions (CAPAs).
• Conduct internal audits and support external regulatory inspections.
• Provide quality assurance guidance to R&D, manufacturing, and other departments.
• Ensure compliance with cGMP, ICH guidelines, and other applicable regulations.
• Develop and update Standard Operating Procedures (SOPs) and quality policies.
• Participate in risk assessments and quality risk management activities.
• Train personnel on quality assurance principles and practices.
• Monitor and report on key quality metrics and performance indicators.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science discipline.
• Minimum of 6 years of experience in Pharmaceutical Quality Assurance/Quality Control.
• In-depth knowledge of cGMP, ICH guidelines, and regulatory requirements (FDA, EMA).
• Proven experience with QMS, batch record review, deviation management, and CAPA.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong documentation and technical writing skills.
• Ability to work independently and manage time effectively in a remote environment.
• Exceptional communication and interpersonal skills.
• Experience with auditing (internal and external) is highly desirable.
• Detail-oriented with a strong commitment to quality and compliance.

• Oversee and maintain the company's Quality Management System (QMS).
• Review and approve batch records, validation protocols, and technical documentation.
• Manage deviations, investigations, CAPA (Corrective and Preventive Actions), and change control processes.
• Conduct internal audits and support external regulatory inspections.
• Ensure compliance with cGMP, ICH guidelines, and other relevant regulations.
• Participate in the qualification and validation of equipment and processes.
• Provide quality assurance support to manufacturing and development teams.
• Contribute to the continuous improvement of quality processes.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related science.
• Significant experience (6+ years) in Quality Assurance within the pharmaceutical or biotechnology industry.
• In-depth knowledge of GMP regulations and quality systems.
• Experience with electronic QMS and LIMS systems is a plus.
• Strong analytical, problem-solving, and documentation skills.
• Excellent communication and interpersonal abilities.

• Job Title: Quality Control Inspector (Late shift)
• Location:Romford,Havering
• Hours: 5pm to 3.15am Monday to Thursday
• Salary: 40K - 50K (This inclues the late shift premium

Job Overview:

Quality Control Inspector will be responsible for the control and compliance of product within the Quality Control inspection department in accordance with current manufacturing and Quality assurance procedures; engineering drawing and customer requirements.

Key Responsibilities:

• Verify the conformity of parts, assemblies and sub-assemblies in line with engineering drawings, the quality management system and any special customer requirements.
• Responsible for comprehensive completion and auditable traceability of inspection records.
• Support Production with the timely verification of batch first off.
• Create and compile First Article Inspection Reports (FAIRs).
• Carry out inspection duties across all areas of the manufacturing and supply chain process as required.
• Identify and report non conformance as per the Company procedure.
• Ensure compliance with Quality Assurance and HSE policies and procedures at all times.
• Processing process and return (P&R) documentation for parts despatched for external processing.

Key Skills and Experience:

• Able to interpret and understand technical data including customer drawings, specifications and FAIR documentation.
• Experienced and familiar with goods inward inspection of finished products / components.
• Experience with aerospace customers and suppliers preferred but not essential.
• Experience of inspecting precision components ensuring adherence to drawing requirements.
• Experience of setting and using a wide variety of direct inspection gauges and measuring equipment.
• Experience of Co-ordinate Measuring Machine (CMM) operation.
• Experience with Sheet Metal / Fabricated parts

For more information about this role please apply here.

Actio recruitment are a recuitment agency and an equal opportunies employer.

• Job Title: Quality Control Inspector (Late shift)
• Location:Romford,Havering
• Hours: 5pm to 3.15am Monday to Thursday
• Salary: 40K - 50K (This inclues the late shift premium

Job Overview:

Quality Control Inspector will be responsible for the control and compliance of product within the Quality Control inspection department in accordance with current manufacturing and Quality assurance procedures; engineering drawing and customer requirements.

Key Responsibilities:

• Verify the conformity of parts, assemblies and sub-assemblies in line with engineering drawings, the quality management system and any special customer requirements.
• Responsible for comprehensive completion and auditable traceability of inspection records.
• Support Production with the timely verification of batch first off.
• Create and compile First Article Inspection Reports (FAIRs).
• Carry out inspection duties across all areas of the manufacturing and supply chain process as required.
• Identify and report non conformance as per the Company procedure.
• Ensure compliance with Quality Assurance and HSE policies and procedures at all times.
• Processing process and return (P&R) documentation for parts despatched for external processing.

Key Skills and Experience:

• Able to interpret and understand technical data including customer drawings, specifications and FAIR documentation.
• Experienced and familiar with goods inward inspection of finished products / components.
• Experience with aerospace customers and suppliers preferred but not essential.
• Experience of inspecting precision components ensuring adherence to drawing requirements.
• Experience of setting and using a wide variety of direct inspection gauges and measuring equipment.
• Experience of Co-ordinate Measuring Machine (CMM) operation.
• Experience with Sheet Metal / Fabricated parts

For more information about this role please apply here.

Actio recruitment are a recuitment agency and an equal opportunies employer.

ROLE OVERVIEW

An exciting role has arisen for a QC Analyst to join a leading Pharmaceutical company based in the Hertfordshire area. As the QC Analyst, you will be responsible for contributing to the Pharmaceutical Development and Support (PDS) department.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the QC Analyst will be varied; however, the key duties and responsibilities are as follows:

1. Conduct Quality Control of raw materials, bulk, and finished products using HPLC, GC, and wet chemical techniques in accordance with authorised test procedures.

2. Analyse products to provide stability data for new product development and ongoing stability monitoring of commercial products, ensuring compliance with authorised test procedures.

3. Perform manual and automated tests and assays with a high level of accuracy and precision, adhering to GMP standards, and operate associated analytical equipment.

4. Collect, process, and report data using software packages such as Chromeleon, LIMS, Excel, and Word, and participate in the overall running of the laboratory, including equipment maintenance and calibration.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the QC Analyst we are looking to identify the following on your profile and past history:

1. Relevant degree in a chemistry-based discipline.

2. Proven industry experience in an analytical testing role, preferably in a GMP environment.

3. A working knowledge and practical experience with HPLC and GC analysis, as well as Microsoft Office, particularly Word and Excel.

Key Words:

Laboratory Analyst / Quality Control / HPLC / GC / Wet Chemical Techniques / GMP / Pharmaceutical Development / Stability Data / Chromeleon / LIMS / Analytical Testing

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.