15 Manufacturing Companies jobs in Cross Hills

• Performing quality inspections and tests on raw materials, components, and finished products.
• Using measuring instruments and testing equipment to verify specifications.
• Documenting inspection results, including measurements, observations, and any non-conformities.
• Identifying defects and non-conforming products, and initiating corrective actions.
• Collaborating with production teams to address quality issues and implement preventative measures.
• Ensuring compliance with quality control procedures, industry standards, and regulatory requirements.
• Maintaining accurate records of inspection activities and quality data.
• Contributing to the continuous improvement of quality management systems.
• Participating in internal audits and quality review meetings.
• Assisting in the development and refinement of inspection protocols.

• Previous experience as a Quality Control Inspector or in a similar quality assurance role within manufacturing.
• Proficiency in using measurement tools (e.g., calipers, micrometers) and testing equipment.
• Strong understanding of quality control principles and methodologies.
• Excellent attention to detail and accuracy in recording data.
• Ability to read and interpret technical drawings and specifications.
• Good communication and interpersonal skills.
• Basic computer literacy, including experience with spreadsheets.
• A commitment to workplace safety and quality standards.

Are you looking for some further experience in Pharmaceutical QC? Do you have prior experience with GC & HPLC in a cGMP environment?

A Global Pharmaceutical Manufacturer are seeking a QC Analyst to join the team at their site in Kirklees. This is a 6 month FTC and would be ideal if you are immediately available and looking to add to your existing experience in Pharmaceutical QC.

Role Overview

• Full Time , 6 month Fixed term Contract. Day Shifts. £27,000pa.
• Analysis of Raw Materials and Finished Products to SOPs.
• Utilise analytical equipment , predominantly HPLC & GC.
• Interpretation and checking of Analytical Data.
• Monitoring, Calibration and occasional basic troubleshooting/maintenance of instruments and analytical equipment.
• Preparation of all relevant documentation in line with applicable standards.

Requirements

• Prior working experience in a cGMP environment using HPLC and GC is essential.
• Degree or equivalent in relevant scientific discipline (or equivalent working experience) is essential.
• Ability to work independently in time pressured environment.
• Excellent communication skills and attention to detail.

In return

This 6 month FTC is an excellent opportunity to add some additional experience to your CV, working alongside industry leaders in a well renowned pharmaceutical organisation.

For more information, please contact Louis Williams

If this QC Analyst job is not quite right for you, but you’re interested in similar opportunities, please take a look at our other Jobs in the Pharmaceutical Sector. Network Scientific is a multi-award-winning recruitment agency dedicated to connecting top talent with opportunities across the scientific and technical sectors. We specialise in temporary, permanent, and contract placements, and pride ourselves on being an ethical and knowledgeable consultancy with a strong focus on candidate care.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the country specified. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

• Oversee and perform a wide range of quality control tests on raw materials, in-process samples, and finished products using various analytical techniques.
• Develop, validate, and implement new testing methods and procedures according to regulatory guidelines (e.g., GMP, ICH).
• Train and mentor junior QC analysts, providing guidance on testing protocols, equipment usage, and data interpretation.
• Review and approve analytical test results, ensuring accuracy, completeness, and compliance with specifications.
• Manage and maintain laboratory equipment, including calibration, preventative maintenance, and troubleshooting.
• Investigate out-of-specification (OOS) results and deviations, determining root causes and implementing corrective and preventative actions (CAPAs).
• Participate in internal and external audits, ensuring the QC laboratory is inspection-ready.
• Maintain accurate and detailed laboratory records, including raw data, reports, and certificates of analysis.
• Contribute to the continuous improvement of QC processes and systems.
• Liaise with R&D, production, and regulatory affairs departments on quality-related matters.
• Ensure compliance with all health, safety, and environmental regulations within the laboratory.

• Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline.
• Minimum of 5 years of experience in a pharmaceutical Quality Control laboratory setting.
• Extensive hands-on experience with analytical techniques such as HPLC, GC, UV-Vis spectroscopy, FTIR, and dissolution testing.
• Thorough understanding of Good Manufacturing Practices (GMP), regulatory guidelines, and quality management systems.
• Proven ability to develop and validate analytical methods.
• Experience in investigating OOS results and deviations.
• Strong leadership, problem-solving, and decision-making skills.
• Excellent attention to detail and organizational abilities.
• Proficiency in using laboratory information management systems (LIMS) and standard laboratory software.
• Effective communication and interpersonal skills for team collaboration and interdepartmental liaison.

• Performing visual and dimensional inspections of incoming materials, components, and finished products using precision measuring instruments.
• Conducting in-process quality checks at various stages of the manufacturing cycle.
• Documenting inspection results accurately and comprehensively in the quality management system.
• Identifying and segregating non-conforming materials or products, initiating corrective action requests as needed.
• Calibrating and maintaining inspection equipment to ensure accuracy and reliability.
• Assisting in the investigation of quality issues and contributing to the implementation of corrective and preventative actions (CAPA).
• Reviewing production documentation to ensure compliance with specifications and quality standards.
• Participating in internal audits and quality improvement initiatives.
• Communicating effectively with production staff and other departments regarding quality matters.
• Adhering strictly to all safety regulations and company policies.

• Develop and implement comprehensive quality control procedures and standards.
• Oversee all aspects of the Quality Management System (QMS).
• Manage and mentor a team of quality control inspectors and technicians.
• Conduct regular inspections and testing of raw materials, in-process materials, and finished goods.
• Analyze production data to identify trends and areas for quality improvement.
• Lead quality improvement initiatives and projects.
• Ensure compliance with relevant industry standards and regulations (e.g., ISO 9001).
• Conduct internal audits and manage external audit processes.
• Investigate customer complaints and non-conformance issues, implementing corrective and preventive actions (CAPA).
• Prepare detailed quality reports for senior management.

• Bachelor's degree in Engineering, Manufacturing, Quality Management, or a related technical field.
• Minimum of 6 years of experience in quality control or quality assurance within a manufacturing environment.
• Proven experience in developing and implementing Quality Management Systems (QMS).
• Strong knowledge of ISO 9001 standards and other relevant industry regulations.
• Proficiency in Statistical Process Control (SPC) and Quality Tools (e.g., Six Sigma, Lean Manufacturing).
• Excellent leadership, team management, and motivational skills.
• Strong analytical, problem-solving, and decision-making abilities.
• Proficiency in quality control software and data analysis tools.
• Excellent written and verbal communication skills.
• Detail-oriented with a strong commitment to quality excellence.

• Develop, implement, and maintain the company's quality management system (QMS) in accordance with relevant industry standards (e.g., ISO 9001).
• Establish and monitor quality control procedures throughout the manufacturing process, from raw material inspection to finished goods testing.
• Conduct regular internal audits to ensure compliance with quality standards and identify areas for improvement.
• Investigate customer complaints and non-conformance issues, implementing corrective and preventive actions (CAPA).
• Train and supervise the quality control team, providing guidance and ensuring efficient workflow.
• Oversee the calibration and maintenance of all quality control equipment and instrumentation.
• Analyse production data to identify trends, root causes of defects, and opportunities for process improvement.
• Collaborate with production, engineering, and procurement teams to ensure quality standards are met at all stages.
• Prepare quality reports for senior management, highlighting key performance indicators (KPIs) and areas of concern.
• Ensure the company adheres to all relevant health, safety, and environmental regulations concerning production quality.

• Bachelor's degree in Engineering, Manufacturing Technology, or a related field.
• Minimum of 5 years of experience in quality control or quality assurance within a manufacturing setting.
• Proven experience with ISO 9001 or other relevant quality management systems.
• Strong understanding of manufacturing processes and quality control techniques.
• Excellent analytical, problem-solving, and decision-making skills.
• Effective leadership, communication, and interpersonal abilities.
• Proficiency in quality management software and data analysis tools.

• Develop, implement, and maintain quality control inspection procedures and standards.
• Conduct thorough inspections and testing of raw materials, in-process components, and finished products.
• Utilise a variety of measuring and testing equipment (e.g., calipers, micrometres, CMMs, visual inspection tools) to ensure product conformity.
• Analyse inspection results, identify trends, and document non-conformities.
• Collaborate closely with production, engineering, and R&D teams to address quality issues and implement corrective actions.
• Participate in root cause analysis for quality failures and recommend preventive measures.
• Ensure compliance with relevant industry standards (e.g., ISO 9001) and regulatory requirements.
• Maintain accurate and detailed quality records, including inspection reports and certificates of analysis.
• Train and mentor junior quality control inspectors.
• Contribute to the continuous improvement of quality management systems and processes.
• Perform internal audits to assess the effectiveness of quality procedures.
• Review and approve production documentation for quality compliance.
• Stay updated on the latest quality control techniques and technologies.

• Proven experience as a Quality Control Inspector or similar role in a manufacturing environment, with a minimum of 5 years in a senior capacity.
• Strong knowledge of quality management systems (e.g., ISO 9001, AS9100).
• Proficiency in using a wide range of precision measuring instruments and testing equipment.
• Experience with statistical process control (SPC) techniques.
• Ability to read and interpret technical drawings, specifications, and blueprints.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong attention to detail and accuracy.
• Effective communication and interpersonal skills for remote collaboration with diverse teams.
• Ability to work independently, manage workload efficiently, and meet deadlines in a remote setting.
• Relevant certifications in quality control (e.g., CQI) are a plus.
• Experience with CMM programming is highly desirable.

• Performing a wide range of analytical tests on raw materials, intermediates, and finished pharmaceutical products using various techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Developing, validating, and transferring analytical methods according to ICH guidelines.
• Interpreting analytical data, preparing comprehensive reports, and documenting all activities accurately.
• Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPAs).
• Ensuring all QC activities comply with cGMP, regulatory requirements, and internal procedures.
• Mentoring and training junior QC scientists and technicians.
• Collaborating with R&D, manufacturing, and regulatory affairs departments.
• Participating in internal and external audits.
• Maintaining laboratory equipment and ensuring its calibration and performance.
• Contributing to the continuous improvement of QC processes and methodologies.

• Perform analytical testing of raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Develop, validate, and transfer analytical methods according to ICH guidelines and regulatory requirements.
• Prepare reagents, standards, and samples for analysis.
• Accurately record, review, and report test results, ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Troubleshoot analytical instrumentation and resolve deviations or out-of-specification (OOS) results.
• Maintain laboratory equipment and ensure its calibration and suitability for use.
• Participate in stability studies and environmental monitoring programs.
• Contribute to the investigation of quality-related issues and the implementation of corrective and preventative actions (CAPAs).
• Stay abreast of current scientific literature, regulatory guidelines, and advancements in analytical chemistry.
• Mentor junior analysts and provide technical training as needed.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, Analytical Chemistry, or a related discipline.
• Minimum of 4-6 years of experience in a pharmaceutical Quality Control laboratory setting.
• Extensive hands-on experience with analytical techniques and instrumentation, particularly HPLC and GC.
• Strong understanding of GMP, GLP, and relevant regulatory guidelines (e.g., FDA, EMA, ICH).
• Proficiency in data analysis and interpretation, with the ability to troubleshoot effectively.
• Excellent attention to detail and accuracy in experimental work and documentation.
• Strong written and verbal communication skills.
• Ability to work effectively both independently and as part of a collaborative team.
• Experience with method development and validation is a significant advantage.
• Knowledge of relevant pharmacopoeias (e.g., USP, EP) is essential.