What Jobs are available for Manufacturing Companies in Leyland?
Showing 5 Manufacturing Companies jobs in Leyland
Quality Control Analyst
Liverpool, North West
SRG
Posted 10 days ago
Job Viewed
Job Description
- 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
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Remote Pharmaceutical Quality Control Scientist
M1 1AE Manchester, North West
£45000 Annually
WhatJobs Direct
Posted 1 day 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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Senior Pharmaceutical Quality Control Analyst
M1 1AA Manchester, North West
£40000 Annually
WhatJobs
Posted 26 days ago
Job Viewed
Job Description
Our client is a leading pharmaceutical company committed to developing and manufacturing high-quality medicines that improve patient lives. We are seeking a meticulous and dedicated Senior Pharmaceutical Quality Control Analyst to join our state-of-the-art laboratory facility. This role is essential for ensuring the safety, efficacy, and quality of our pharmaceutical products through rigorous testing and analysis. The ideal candidate will have substantial experience in a QC laboratory environment, with a strong understanding of analytical techniques commonly used in the pharmaceutical industry, such as HPLC, GC, spectroscopy, and wet chemistry methods. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products. Your duties will include method development and validation, instrument calibration and maintenance, data review and approval, and ensuring compliance with Good Manufacturing Practices (GMP) and regulatory guidelines. The ability to accurately interpret complex data, troubleshoot analytical issues, and maintain detailed laboratory records is crucial. As a senior member of the team, you will also be expected to mentor junior analysts, contribute to quality improvement initiatives, and participate in internal audits. This is a hands-on role that requires precision, attention to detail, and a strong commitment to scientific integrity. We are looking for an individual who is passionate about quality and plays a vital role in safeguarding public health. Collaboration with R&D, manufacturing, and regulatory affairs departments is also a key aspect of this position. Your dedication to upholding the highest standards will be instrumental in our mission to deliver safe and effective pharmaceutical solutions.
Responsibilities:
Responsibilities:
- 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.
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2
Senior Pharmaceutical Quality Control Analyst (Remote)
L2 0AN Liverpool, North West
£50000 Annually
WhatJobs
Posted 23 days ago
Job Viewed
Job Description
Our client is actively seeking a highly experienced Senior Pharmaceutical Quality Control Analyst to join their dedicated team on a fully remote basis. This critical role will involve ensuring the highest standards of quality for our pharmaceutical products through rigorous analytical testing and data interpretation. The successful candidate will be instrumental in maintaining regulatory compliance and driving continuous improvement within our quality control processes, all managed from the comfort of their home office.
Key responsibilities include:
The ideal candidate will hold a Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related scientific discipline. A minimum of 7 years of progressive experience in pharmaceutical quality control is required, with a strong emphasis on analytical method development and validation. Demonstrated expertise in GMP/GLP environments and thorough knowledge of regulatory requirements are essential. Excellent analytical, problem-solving, and communication skills are paramount for success in this remote position. Candidates must possess a dedicated home office setup with reliable internet connectivity, enabling seamless participation in virtual meetings and access to company systems. This is an exceptional opportunity for a seasoned professional to contribute significantly to a leading pharmaceutical organization while enjoying the flexibility of a remote work arrangement.
Key responsibilities include:
- 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.
The ideal candidate will hold a Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related scientific discipline. A minimum of 7 years of progressive experience in pharmaceutical quality control is required, with a strong emphasis on analytical method development and validation. Demonstrated expertise in GMP/GLP environments and thorough knowledge of regulatory requirements are essential. Excellent analytical, problem-solving, and communication skills are paramount for success in this remote position. Candidates must possess a dedicated home office setup with reliable internet connectivity, enabling seamless participation in virtual meetings and access to company systems. This is an exceptional opportunity for a seasoned professional to contribute significantly to a leading pharmaceutical organization while enjoying the flexibility of a remote work arrangement.
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3
Remote Senior Quality Control Inspector - Manufacturing
N/A Liverpool, North West
£35000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client is seeking a dedicated and experienced Senior Quality Control Inspector to join their remote manufacturing team. This is a fully remote position, allowing you to contribute to ensuring product quality and adherence to stringent standards from your home office. You will be responsible for performing detailed inspections, analysing data, and contributing to the continuous improvement of quality processes within the manufacturing operations. This role requires a meticulous eye for detail and a deep understanding of quality control methodologies.
Key Responsibilities:
Key Responsibilities:
- 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.
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