What Jobs are available for Manufacturing Companies in Oldham?
Showing 11 Manufacturing Companies jobs in Oldham
Quality Control Reviewer
Bioscript Group
Posted 7 days ago
Job Viewed
Job Description
Role: Quality Control Reviewer
Business Unit: Bioscript Regulatory Writing
Location: Macclesfield / London (Hybrid or remote - UK)
About Us
Established in 2005, Bioscript Group is formed from multiple, specialist businesses to support our global pharmaceutical clients; we draw on their multidisciplinary expertise to help navigate critical decisions at key points in the product lifecycle.
Our scientific and strategic expertise helps our clients make better decisions. We provide medical communication services, market access consulting and regulatory writing support with deep domain expertise to effectively navigate complex disease areas.
The Opportunity
The role of the Quality Control Reviewer is to conduct quality control (QC) and other supportive activities to support delivery of accurate, compliant and submission-ready documents prepared by writers in Bioscript Regulatory Writing (including internal and external writers), or by clients.
Key Responsibilities
- Perform QC review and manage QC projects in accordance with agreed upon timelines.
- Verify accuracy of document content using source documents including, but not limited to, clinical regulatory documents (e.g. protocols, clinical study reports, CIOMS reports, clinical summaries/overviews), statistical analysis plans and data tables, figures, and listings.
- Verify internal consistency within a document and across related documents.
- Verify uniformity and compliance of documents with internal or client standards (e.g. document templates, style guide, publishing requirements).
- Record QC findings and identify appropriate corrections to address findings.
- Collaborate with document authors and other team members (as needed) to resolve QC findings.
- Proactively share knowledge and experience to support transfer of knowledge across the team.
- Take responsibility for ensuring optimum use of own time. Flag capacity or bottlenecks to the QC Manager so that resource can be allocated most efficiently. Efficiently manage competing projects, proactively flagging potential issues to the QC Manager.
- Support the Project Management team by monitoring the progress of all assigned projects against the agreed QC schedule and QC budget specification.
- Support the regulatory writing team (eg, supporting other QC Reviewers, editorial support for writers (eg, populating tables, drafting narratives etc).
- Understand QC and publishing processes and strategy, client procedures, and best practice for projects.
- Proofread, edit, compile, and publish regulatory documents according to BRW or client conventions and applicable regulatory and industry guidance.
- Ensure adherence to agreed client/Bioscript standard operating procedures.
About You
- Previous experience working as a QC Reviewer / Regulatory Writer within an agency or pharmaceutical setting
- Previous experience of document publishing preferred
- Attention to detail to ensure accuracy and quality in all deliverables
- Ability to take initiative and manage multiple tasks independently
- Strong communication skills
Our people are at the heart of our business
We are focused not just on delivering the exceptional for our clients, but for our teams too. We understand everyone is different and believe in treating everyone as an individual with opportunities to develop your skills and career around our disciplines.
Our benefits include:
- Salary which aligns with your experience and skillset
- 25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
- Enhanced sick and compassionate leave
- Enhanced maternity, paternity & adoption leave
- Birthday charity donation to a charity of your choice
- Bonus Day off to be spent giving back to the community
- Life Insurance and Critical Illness cover
- Private Medical (Vitality for UK based colleagues)
- Health cash plan or wellbeing allowance
- International Employee Assistance Program
We are committed to creating an inclusive and diverse workplace. We encourage applications from all individuals who meet the minimum requirements of the role. If you require any reasonable adjustments during the application or interview process, please contact us via or by calling .
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0
Senior Quality Control Manager
BD5 8DA Bradford, Yorkshire and the Humber
£60000 Annually
WhatJobs Direct
Posted today
Job Viewed
Job Description
Our client, a leading manufacturing firm, is seeking an experienced Senior Quality Control Manager to oversee all aspects of quality assurance for their production facility. This critical role is based at their site in **Bradford, West Yorkshire, UK**, and involves ensuring that all products meet stringent quality standards and regulatory requirements. The successful candidate will lead a team of quality inspectors and technicians, implement continuous improvement initiatives, and maintain a strong quality culture.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and manage the company's Quality Management System (QMS).
- Establish and maintain quality control procedures and standards throughout the manufacturing process.
- Lead and mentor the Quality Control team, including inspectors, technicians, and auditors.
- Conduct regular quality audits of internal processes and supplier performance.
- Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA).
- Ensure compliance with relevant industry standards and certifications (e.g., ISO 9001).
- Manage the inspection and testing of raw materials, in-process materials, and finished goods.
- Investigate customer complaints and non-conformances, and implement solutions to prevent recurrence.
- Collaborate with Production, Engineering, and R&D departments to improve product quality and reduce defects.
- Oversee the calibration and maintenance of testing equipment.
- Prepare quality reports for senior management, highlighting key metrics and areas for improvement.
- Promote a quality-first mindset throughout the organization.
- Bachelor's degree in Engineering, Science, or a related technical field.
- Minimum of 8 years of progressive experience in Quality Control or Quality Assurance within a manufacturing environment.
- Proven experience in managing and leading a QC/QA team.
- In-depth knowledge of Quality Management Systems (QMS) and relevant standards (e.g., ISO 9001).
- Strong understanding of statistical quality control (SQC) and Six Sigma methodologies.
- Experience with various inspection and testing techniques.
- Excellent analytical, problem-solving, and decision-making skills.
- Proficient in using quality management software and data analysis tools.
- Strong leadership, communication, and interpersonal skills.
- Ability to effectively implement change and drive continuous improvement.
- Familiarity with regulatory requirements specific to the manufacturing sector is essential.
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1
Lead Quality Control Specialist
BD3 7AE Bradford, Yorkshire and the Humber
£40000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a reputable pharmaceutical manufacturer committed to producing high-quality medicines, is seeking a dedicated and experienced Lead Quality Control Specialist to join their team in Bradford, West Yorkshire, UK . This vital on-site role involves ensuring that all manufactured products meet stringent regulatory standards and internal quality benchmarks.
Responsibilities:
Responsibilities:
- 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.
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2
Senior Quality Control Manager
BD1 1DL Bradford, Yorkshire and the Humber
£50000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a leader in the manufacturing industry, is seeking a meticulous and experienced Senior Quality Control Manager to oversee quality assurance processes at their facility in Bradford, West Yorkshire, UK . This critical role ensures that all manufactured products meet stringent quality standards and regulatory requirements. You will be responsible for developing, implementing, and maintaining the company's quality management system (QMS), including ISO certifications. Your duties will involve overseeing inspection and testing procedures, analyzing production data to identify areas for improvement, and leading quality improvement initiatives. You will manage a team of quality control inspectors and technicians, providing guidance, training, and performance management. The ideal candidate will have a deep understanding of manufacturing processes, quality control methodologies, and statistical process control (SPC). You will collaborate closely with production, engineering, and supply chain departments to resolve quality issues and prevent their recurrence. This role also involves conducting internal audits, preparing quality reports for management, and ensuring compliance with industry-specific regulations. A proactive approach to identifying and mitigating quality risks is essential. You should possess strong leadership skills, excellent analytical abilities, and a commitment to continuous improvement. The ability to foster a quality-focused culture throughout the organization is paramount.
Responsibilities:
Responsibilities:
- 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.
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3
Remote Pharmaceutical Quality Control Manager
BD1 1AG Bradford, Yorkshire and the Humber
£75000 Annually
WhatJobs Direct
Posted 2 days ago
Job Viewed
Job Description
Our client, a rapidly expanding pharmaceutical innovator, is seeking a highly experienced and diligent Remote Pharmaceutical Quality Control Manager. This pivotal role is responsible for ensuring the integrity, safety, and efficacy of pharmaceutical products through robust quality control processes, all managed within a fully remote framework. You will lead and manage a dispersed team of QC analysts, oversee the implementation and maintenance of the Quality Management System (QMS), and ensure compliance with global regulatory standards (e.g., FDA, EMA, MHRA). Your responsibilities will include developing and validating analytical methods, interpreting complex test results, conducting deviation investigations, and authoring quality control reports. The ideal candidate will possess a PhD or Master's degree in Pharmaceutical Sciences, Chemistry, or a closely related field, with substantial experience in pharmaceutical quality control and assurance. A deep understanding of ICH guidelines, GMP, and analytical techniques such as HPLC, GC, spectroscopy, and dissolution testing is essential. As a remote manager, you must demonstrate exceptional leadership skills, the ability to motivate and guide a remote workforce, and outstanding communication capabilities to foster a culture of quality across the organisation. Proficiency in electronic QMS software and data analysis tools is highly desirable. You will play a critical role in batch release decisions, supplier qualification, and continuous improvement initiatives. This position requires a proactive, detail-oriented individual capable of making critical decisions based on scientific data and regulatory requirements. Join a forward-thinking company dedicated to advancing healthcare through rigorous quality standards, all while working from your preferred location.
Key Responsibilities:
Key Responsibilities:
- Manage and lead a remote team of Quality Control analysts.
- Oversee the development, validation, and execution of analytical test methods.
- Ensure compliance with GMP, ICH, and other regulatory guidelines.
- Review and approve QC data, batch records, and documentation.
- Lead investigations into out-of-specification (OOS) results and deviations.
- Author and maintain quality control procedures and reports.
- Manage the stability testing program.
- Collaborate with other departments (e.g., R&D, Manufacturing, Regulatory Affairs).
- Contribute to the improvement of the Quality Management System.
- PhD or MSc in Pharmaceutical Sciences, Chemistry, or related discipline.
- Significant experience in pharmaceutical Quality Control (QC) and Quality Assurance (QA).
- Extensive knowledge of analytical techniques (HPLC, GC, spectroscopy, etc.).
- In-depth understanding of GMP, ICH guidelines, and regulatory requirements.
- Proven experience in managing QC teams, preferably in a remote setting.
- Excellent leadership, communication, and problem-solving skills.
- Proficiency in electronic QMS and data analysis software.
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4
Remote Pharmaceutical Quality Control Scientist
M1 1AE Manchester, North West
£45000 Annually
WhatJobs Direct
Posted 2 days ago
Job Viewed
Job Description
We are seeking a dedicated and detail-oriented Pharmaceutical Quality Control Scientist to join our dynamic, remote-based team. This role is crucial in ensuring the quality and safety of our pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests, documenting results accurately, and ensuring compliance with all regulatory standards and internal procedures. This position offers the unique advantage of working remotely while contributing to vital pharmaceutical development.
Key Responsibilities:
Qualifications:
This exciting remote opportunity allows you to apply your scientific expertise from the comfort of your home. Our client is a leader in the pharmaceutical industry, committed to innovation and employee well-being. If you are a motivated scientist with a passion for quality and a desire for remote work flexibility, we encourage you to apply.
Key Responsibilities:
- 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.
Qualifications:
- 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.
This exciting remote opportunity allows you to apply your scientific expertise from the comfort of your home. Our client is a leader in the pharmaceutical industry, committed to innovation and employee well-being. If you are a motivated scientist with a passion for quality and a desire for remote work flexibility, we encourage you to apply.
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5
Senior Pharmaceutical Quality Control Analyst
BD1 4SJ Bradford, Yorkshire and the Humber
£45000 Annually
WhatJobs
Posted 12 days ago
Job Viewed
Job Description
Our client, a reputable pharmaceutical company based in Bradford, West Yorkshire, UK , is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Control Analyst. This critical role involves ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a wide range of analytical tests, validating methods, troubleshooting laboratory equipment, and ensuring compliance with Good Laboratory Practices (GLP) and regulatory standards. The ideal candidate possesses a strong background in pharmaceutical analysis, excellent attention to detail, and a commitment to maintaining the highest quality standards in a highly regulated environment. This role requires hands-on laboratory work.
Responsibilities:
Responsibilities:
- Perform analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, dissolution).
- Validate analytical methods and equipment according to regulatory guidelines.
- Troubleshoot and maintain laboratory instruments, ensuring they are calibrated and functioning correctly.
- Interpret test results, document findings accurately, and prepare detailed analytical reports.
- Ensure all laboratory activities comply with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory requirements.
- Review and approve test data generated by junior analysts.
- Participate in investigations of out-of-specification (OOS) results and implement corrective actions.
- Contribute to the continuous improvement of laboratory processes and procedures.
- Maintain accurate and organized laboratory records.
- Assist in training and mentoring junior QC analysts.
- Liaise with other departments, such as production and R&D, regarding quality control matters.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 5 years of experience in pharmaceutical quality control or a related analytical laboratory role.
- Strong practical experience with analytical instrumentation (HPLC, GC, spectrophotometry, etc.).
- Thorough understanding of GLP, GMP, and relevant pharmaceutical regulatory guidelines (e.g., FDA, EMA).
- Excellent attention to detail and accuracy in data recording and analysis.
- Strong problem-solving and troubleshooting skills.
- Ability to work independently and manage multiple tasks effectively.
- Good written and verbal communication skills.
- Proficiency in using laboratory information management systems (LIMS) is a plus.
- Experience with method validation and transfer is highly desirable.
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6
Senior Pharmaceutical Quality Control Analyst
BD1 1AA Bradford, Yorkshire and the Humber
£45000 Annually
WhatJobs
Posted 13 days ago
Job Viewed
Job Description
Our client, a dynamic pharmaceutical company, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in **Bradford, West Yorkshire, UK**. This is a key role within our Quality Assurance department, responsible for ensuring the quality and compliance of our pharmaceutical products throughout the manufacturing process. You will lead a team of analysts, oversee routine testing, method development, and validation activities, and contribute to continuous improvement initiatives. The ideal candidate will possess a strong scientific background, extensive experience in pharmaceutical QC, and a thorough understanding of GMP regulations. Responsibilities include:
- Supervising and mentoring junior QC analysts, providing technical guidance and support.
- Developing, validating, and implementing analytical methods for raw materials, in-process samples, and finished products.
- Performing complex analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, and KF titration.
- Reviewing and approving analytical data, ensuring accuracy and compliance with specifications.
- Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPAs).
- Maintaining laboratory equipment, ensuring calibration and qualification are up to date.
- Preparing and reviewing QC-related documentation, including SOPs, validation reports, and stability protocols.
- Ensuring all activities are conducted in compliance with Good Manufacturing Practices (GMP) and relevant regulatory guidelines (e.g., MHRA, FDA).
- Participating in internal and external audits.
- Contributing to process improvement projects to enhance efficiency and quality.
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7
Senior Pharmaceutical Quality Control Analyst
BD3 0LP Bradford, Yorkshire and the Humber
£40000 Annually
WhatJobs
Posted 22 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to developing life-changing medicines, is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join their dynamic team in Bradford, West Yorkshire, UK . This is a critical role responsible for ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. The successful candidate will play a key role in maintaining compliance with regulatory standards and internal quality management systems. This position requires a strong background in analytical chemistry, pharmaceutical science, and a thorough understanding of GMP (Good Manufacturing Practice) guidelines. This is an on-site role, offering the opportunity to work within state-of-the-art laboratory facilities.
Responsibilities:
Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
- Develop, validate, and transfer analytical methods according to ICH guidelines.
- Calibrate and maintain laboratory equipment, ensuring it is in optimal working condition.
- Interpret test results, document findings accurately in laboratory notebooks and electronic systems, and generate certificates of analysis.
- Investigate deviations, out-of-specification (OOS) results, and non-conformances, implementing corrective and preventative actions (CAPAs).
- Review and approve analytical data and documentation.
- Participate in internal and external audits as required.
- Ensure all laboratory activities are conducted in compliance with GMP, regulatory requirements (e.g., MHRA, FDA), and company Standard Operating Procedures (SOPs).
- Assist in the training and mentoring of junior analysts.
- Contribute to continuous improvement initiatives within the Quality Control department.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, Biochemistry, or a related scientific discipline.
- Minimum of 5 years of experience in pharmaceutical Quality Control or Analytical Development.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, etc.) and method validation.
- Thorough understanding of GMP regulations and quality assurance principles in the pharmaceutical industry.
- Strong knowledge of pharmacopoeial methods (e.g., BP, USP, EP).
- Excellent attention to detail, accuracy, and data integrity skills.
- Proficiency in laboratory information management systems (LIMS) and electronic data capture.
- Strong problem-solving and investigative skills.
- Ability to work independently and collaboratively in a fast-paced laboratory environment.
- Excellent written and verbal communication skills.
- This role requires the candidate to work on-site in Bradford, West Yorkshire, UK .
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8
Senior Quality Control Manager - Pharmaceuticals
BD7 1DB Bradford, Yorkshire and the Humber
£65000 Annually
WhatJobs
Posted 25 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical manufacturer, is seeking an experienced and meticulous Senior Quality Control Manager to lead their quality assurance and control operations. This pivotal role ensures that all manufactured products meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory requirements and industry best practices. You will be responsible for developing and implementing robust quality systems, managing the QC laboratory, leading a team of QC analysts, and ensuring compliance with Good Manufacturing Practices (GMP).
Key Responsibilities:
Key Responsibilities:
- Oversee all aspects of the Quality Control department, including raw material testing, in-process testing, and finished product release.
- Develop, validate, and implement analytical methods and procedures in accordance with regulatory guidelines (e.g., FDA, EMA).
- Ensure compliance with cGMP, ICH guidelines, and other relevant pharmaceutical quality standards.
- Manage and mentor a team of Quality Control analysts, providing training, performance management, and technical guidance.
- Lead investigations into out-of-specification (OOS) results and deviations, implementing corrective and preventative actions (CAPAs).
- Oversee the calibration, maintenance, and qualification of laboratory equipment.
- Review and approve analytical data, batch records, and quality reports.
- Liaise with regulatory agencies during inspections and audits.
- Contribute to the development and continuous improvement of the company's Quality Management System (QMS).
- Maintain inventory of laboratory supplies and manage the QC budget effectively.
- Master's degree or PhD in Chemistry, Pharmaceutical Sciences, or a related scientific field.
- Minimum of 7-10 years of progressive experience in Quality Control within the pharmaceutical industry.
- Proven experience in managing a QC laboratory and leading a team of analysts.
- In-depth knowledge of analytical techniques (e.g., HPLC, GC, spectroscopy, dissolution) and their application.
- Strong understanding of cGMP regulations and pharmaceutical quality systems.
- Experience with method validation and OOS investigations is essential.
- Excellent leadership, communication, and interpersonal skills.
- Strong analytical and problem-solving abilities, with a keen eye for detail.
- Proficiency in quality documentation and regulatory reporting.
- Ability to work effectively under pressure and manage multiple priorities.
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