What Jobs are available for Manufacturing Companies in Little Hulton?

• Job Title: QC Specialist – Biosafety
• Location: Speke, Liverpool.
• Contract: until end of July 2026 initially
• Rate: £15.25 (inclusive of shift uplift)
• Shift : 4 on 4 off, 7am-7pm

SRG are currently working with a global pharmaceutical manufacturer based in Liverpool, looking for QC Analyst (Biosafety) to join the team. The site in Speke specialises in the production of sterile injectable products, for the treatment of the flu. This is a fantastic opportunity for a Biological Science graduate with some experience to further their career.

Main responsibilities:

• Performing a range of tests within a highly regulated Quality Control laboratory to GMP regulations.
• Performing routine QC testing
• Documenting laboratory results in an accurate and timely manner.
• Complying with GMP regulatory requirements at all times.

Key requirements:

• Experience of working to GMP/pharmaceutical regulatory requirements is desirable.
• Biological background either from university degree or relevant work in the field
• Computer skills, excel, word, outlook

Preferrable

• Experience within cell cultures and/or assay testing.
• LIMS and SAP

• Perform analytical testing on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques and instrumentation (e.g., HPLC, GC, UV-Vis, Karl Fischer).
• Accurately document all testing procedures, results, and observations in compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
• Prepare reagents, standards, and solutions as required for testing.
• Maintain laboratory equipment, ensuring calibration and proper functioning.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, identifying root causes and recommending corrective actions.
• Participate in method validation and transfer activities.
• Review and approve testing data and associated documentation.
• Ensure adherence to all company SOPs, regulatory guidelines (e.g., FDA, EMA), and safety protocols.
• Contribute to the continuous improvement of quality control processes and systems.
• Collaborate with other departments, including R&D, Production, and Regulatory Affairs, to resolve quality-related issues.
• Maintain a clean and organized remote laboratory workspace.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biotechnology, or a related scientific discipline.
• Minimum of 3-5 years of experience in pharmaceutical quality control or a related analytical laboratory setting.
• Proficiency with common analytical techniques and instrumentation (HPLC, GC are essential).
• Strong understanding of GMP, GLP, and relevant regulatory guidelines.
• Excellent documentation skills and attention to detail.
• Proficiency in data analysis and interpretation.
• Strong problem-solving and critical thinking abilities.
• Ability to work independently and manage time effectively in a remote environment.
• Excellent written and verbal communication skills.
• Familiarity with laboratory information management systems (LIMS) is a plus.

• Perform a variety of analytical tests on raw materials, intermediates, and finished pharmaceutical products.
• Utilize analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, and dissolution apparatus.
• Develop, validate, and transfer analytical methods according to ICH guidelines.
• Calibrate, maintain, and troubleshoot laboratory equipment.
• Review and interpret analytical data, ensuring accuracy and compliance.
• Document all laboratory activities in accordance with GMP requirements.
• Investigate out-of-specification (OOS) results and deviations.
• Contribute to quality improvement initiatives and process optimization.
• Assist in regulatory inspections and internal audits.
• Mentor and train junior Quality Control analysts.

• BSc or MSc in Chemistry, Pharmaceutical Science, or a related discipline.
• Minimum of 5 years of experience in a pharmaceutical Quality Control laboratory.
• Extensive experience with analytical techniques including HPLC, GC, and spectrophotometry.
• Thorough understanding of GMP, ICH guidelines, and regulatory requirements.
• Experience with method validation and troubleshooting.
• Excellent attention to detail and accuracy.
• Strong data analysis and interpretation skills.
• Proficiency in laboratory information management systems (LIMS).
• Good written and verbal communication skills.
• Ability to work independently and as part of a team.

• Performing a wide range of analytical tests on raw materials, in-process samples, and finished products using various techniques (e.g., HPLC, GC, UV-Vis, FTIR, dissolution testing).
• Developing, validating, and transferring analytical methods in accordance with regulatory guidelines (e.g., ICH, FDA, EMA).
• Interpreting complex analytical data, generating comprehensive reports, and investigating out-of-specification (OOS) results.
• Ensuring all laboratory activities are conducted in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Maintaining and calibrating laboratory equipment, troubleshooting instrument issues, and ensuring proper functioning.
• Reviewing and approving analytical data and documentation generated by junior analysts.
• Contributing to regulatory submissions and responding to queries from health authorities.
• Participating in internal and external audits as a subject matter expert.
• Mentoring and training junior QC analysts, providing guidance and technical support.
• Collaborating with other departments, such as R&D, Manufacturing, and Regulatory Affairs, to resolve quality issues.
• Identifying opportunities for process improvements and implementing them to enhance efficiency and accuracy.

• Perform remote visual and instrumental inspections of manufactured components and finished products according to established standards and specifications.
• Analyse inspection data to identify trends, root causes of defects, and areas for process improvement.
• Document inspection results accurately and comprehensively using digital tools and software.
• Collaborate with manufacturing engineers and production teams to address quality issues and implement corrective actions.
• Review and interpret technical drawings, blueprints, and quality standards.
• Assist in the development and implementation of new quality control procedures and test methods.
• Train and mentor junior quality inspectors as needed.
• Ensure compliance with all relevant quality management systems (e.g., ISO 9001).
• Participate in internal and external quality audits.
• Maintain calibration records for inspection equipment used remotely or managed by partners.
• Communicate effectively with cross-functional teams regarding quality performance and concerns.

• Proven experience as a Quality Control Inspector or in a similar role within a manufacturing environment.
• Strong understanding of quality control principles, methodologies, and tools.
• Proficiency in reading and interpreting technical drawings, specifications, and quality standards.
• Experience with various inspection techniques and measurement equipment.
• Excellent analytical and problem-solving skills.
• Meticulous attention to detail and commitment to accuracy.
• Strong documentation and reporting skills.
• Proficiency in using digital quality management systems and relevant software (e.g., Microsoft Office Suite, specialised QC software).
• Excellent communication and interpersonal skills, with the ability to work effectively in a remote team environment.
• Self-motivated, organised, and able to manage workload independently.
• Familiarity with Six Sigma or Lean manufacturing principles is a plus.