What Jobs are available for Manufacturing Companies in Gateshead?
Showing 13 Manufacturing Companies jobs in Gateshead
Senior Quality Control Engineer
NE28 0RA Newcastle upon Tyne, North East
£50000 Annually
WhatJobs Direct
Posted 1 day ago
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Job Description
Our client, a renowned leader in advanced manufacturing based in Newcastle upon Tyne, Tyne and Wear , is looking for a highly experienced Senior Quality Control Engineer to join their dedicated production team. This is a crucial on-site role where your expertise will directly impact the quality and reliability of our high-precision products.
In this role, you will be responsible for developing, implementing, and maintaining robust quality control systems and procedures throughout the entire manufacturing process. You will conduct rigorous inspections and testing of raw materials, in-process components, and finished goods to ensure compliance with stringent industry standards and customer specifications. Your duties will include analysing quality data, identifying root causes of defects, and implementing corrective and preventative actions (CAPA) to drive continuous improvement. You will also lead and mentor junior quality technicians, oversee calibration programs for testing equipment, and prepare detailed quality reports for management. Collaboration with R&D, production, and engineering departments to ensure quality is integrated from product design through to final delivery is a key aspect of this position.
The ideal candidate will possess a Bachelor's degree in Engineering (Mechanical, Manufacturing, or a related field) or an equivalent combination of education and experience. A minimum of 7 years of progressive experience in quality control or quality assurance within a manufacturing environment, preferably in aerospace, automotive, or medical devices, is essential. Strong knowledge of quality management systems (e.g., ISO 9001, AS9100) and statistical process control (SPC) techniques is required. Proficiency in using various inspection tools and measurement equipment, along with excellent analytical, problem-solving, and decision-making skills, are paramount. You should possess exceptional attention to detail, strong leadership capabilities, and the ability to effectively communicate quality standards and findings to all levels of the organisation. Experience with Lean Manufacturing principles and Six Sigma methodologies is highly desirable. This is an excellent opportunity to contribute to a company at the forefront of manufacturing innovation and uphold the highest standards of product excellence.
In this role, you will be responsible for developing, implementing, and maintaining robust quality control systems and procedures throughout the entire manufacturing process. You will conduct rigorous inspections and testing of raw materials, in-process components, and finished goods to ensure compliance with stringent industry standards and customer specifications. Your duties will include analysing quality data, identifying root causes of defects, and implementing corrective and preventative actions (CAPA) to drive continuous improvement. You will also lead and mentor junior quality technicians, oversee calibration programs for testing equipment, and prepare detailed quality reports for management. Collaboration with R&D, production, and engineering departments to ensure quality is integrated from product design through to final delivery is a key aspect of this position.
The ideal candidate will possess a Bachelor's degree in Engineering (Mechanical, Manufacturing, or a related field) or an equivalent combination of education and experience. A minimum of 7 years of progressive experience in quality control or quality assurance within a manufacturing environment, preferably in aerospace, automotive, or medical devices, is essential. Strong knowledge of quality management systems (e.g., ISO 9001, AS9100) and statistical process control (SPC) techniques is required. Proficiency in using various inspection tools and measurement equipment, along with excellent analytical, problem-solving, and decision-making skills, are paramount. You should possess exceptional attention to detail, strong leadership capabilities, and the ability to effectively communicate quality standards and findings to all levels of the organisation. Experience with Lean Manufacturing principles and Six Sigma methodologies is highly desirable. This is an excellent opportunity to contribute to a company at the forefront of manufacturing innovation and uphold the highest standards of product excellence.
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0
Senior Pharmaceutical Quality Control Manager
NE6 1AA Newcastle upon Tyne, North East
£75000 Annually
WhatJobs
Posted 24 days ago
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company committed to improving global health, is seeking an experienced and meticulous Senior Pharmaceutical Quality Control Manager to lead their QC operations in Newcastle upon Tyne, Tyne and Wear, UK . This pivotal role involves overseeing all aspects of quality control testing, ensuring adherence to strict regulatory standards (e.g., GMP, FDA), and maintaining the integrity and safety of pharmaceutical products. You will manage a team of skilled analysts, implement advanced testing methodologies, and contribute significantly to the company's compliance and product excellence.
Key Responsibilities:
The ideal candidate will possess a Master's degree or Ph.D. in Chemistry, Pharmacy, or a related life science discipline. A minimum of 7 years of experience in pharmaceutical quality control, with at least 3 years in a management or supervisory role, is essential. In-depth knowledge of GMP regulations and analytical techniques (HPLC, GC, spectroscopy, wet chemistry) is required. Proven experience in method development, validation, and OOS investigations is critical. Strong leadership, problem-solving, and communication skills are necessary. Experience with pharmaceutical manufacturing processes and quality systems is highly desirable. This is a key leadership position based in Newcastle upon Tyne , offering a competitive salary, excellent benefits, and the opportunity to contribute to life-saving medicines.
Key Responsibilities:
- Lead and manage the day-to-day operations of the Quality Control department, including laboratory testing of raw materials, in-process samples, and finished products.
- Develop, validate, and implement analytical methods according to relevant pharmacopoeias and regulatory guidelines.
- Ensure compliance with Good Manufacturing Practices (GMP) and other applicable regulatory standards.
- Supervise and mentor QC analysts, providing training and performance management.
- Review and approve testing data, batch records, and analytical reports.
- Manage laboratory equipment, ensuring calibration, maintenance, and qualification.
- Investigate Out-of-Specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
- Collaborate with R&D, Production, and Quality Assurance departments to resolve quality issues and support product lifecycle management.
- Maintain accurate and organized laboratory records and documentation.
- Contribute to internal and external audits as a subject matter expert.
- Stay current with scientific advancements and regulatory changes affecting pharmaceutical quality control.
The ideal candidate will possess a Master's degree or Ph.D. in Chemistry, Pharmacy, or a related life science discipline. A minimum of 7 years of experience in pharmaceutical quality control, with at least 3 years in a management or supervisory role, is essential. In-depth knowledge of GMP regulations and analytical techniques (HPLC, GC, spectroscopy, wet chemistry) is required. Proven experience in method development, validation, and OOS investigations is critical. Strong leadership, problem-solving, and communication skills are necessary. Experience with pharmaceutical manufacturing processes and quality systems is highly desirable. This is a key leadership position based in Newcastle upon Tyne , offering a competitive salary, excellent benefits, and the opportunity to contribute to life-saving medicines.
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1
Senior Pharmaceutical Quality Control Analyst
NE1 1 Newcastle upon Tyne, North East
£45000 Annually
WhatJobs
Posted 24 days ago
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Job Description
We are seeking a highly skilled and motivated Senior Pharmaceutical Quality Control Analyst to join a leading pharmaceutical company in **Newcastle upon Tyne, Tyne and Wear, UK**. This critical role involves conducting a wide range of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with stringent quality standards and regulatory requirements. The Senior Analyst will perform analytical testing using various techniques, including HPLC, GC, UV-Vis, FT-IR, and wet chemistry methods. You will be responsible for method validation and transfer, developing and optimizing analytical methods, and troubleshooting instrument issues. Accurate and meticulous documentation of all test results, deviations, and investigations in compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) is paramount. The role also involves reviewing and approving analytical data generated by junior analysts, contributing to internal audits, and participating in regulatory inspections. You will play a key role in the continuous improvement of quality control processes and systems, identifying potential risks and implementing corrective and preventive actions (CAPAs). The ideal candidate will possess a strong understanding of pharmaceutical quality systems, regulatory guidelines (e.g., FDA, EMA), and analytical chemistry principles. Excellent problem-solving skills, attention to detail, and the ability to work independently and as part of a team are essential.
Key Responsibilities:
Qualifications and Experience:
Key Responsibilities:
- Perform analytical testing on raw materials, intermediates, and finished products using various instrumental and wet chemistry techniques (e.g., HPLC, GC, UV-Vis, FT-IR).
- Ensure all testing is conducted in compliance with GMP, GLP, and relevant regulatory guidelines.
- Develop, validate, and transfer analytical methods.
- Troubleshoot and maintain laboratory instrumentation.
- Accurately document and review all experimental data, results, and deviations.
- Investigate out-of-specification (OOS) results and implement corrective actions.
- Review and approve analytical data and reports prepared by junior analysts.
- Participate in internal audits and regulatory inspections.
- Contribute to the continuous improvement of QC processes and laboratory operations.
- Maintain a safe and compliant laboratory environment.
Qualifications and Experience:
- BSc/MSc in Chemistry, Pharmaceutical Science, or a related scientific discipline.
- Minimum 5 years of experience in a pharmaceutical Quality Control laboratory environment.
- Extensive hands-on experience with analytical techniques such as HPLC, GC, spectroscopy, and wet chemistry.
- Strong understanding of GMP, GLP, ICH guidelines, and regulatory requirements.
- Experience with method validation and transfer.
- Proficiency in data analysis and interpretation.
- Excellent documentation skills and attention to detail.
- Strong problem-solving and critical thinking abilities.
- Good communication and interpersonal skills.
- Ability to work independently and collaboratively within a team.
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2
Senior Quality Control Engineer - Advanced Materials
NE1 0PQ Newcastle upon Tyne, North East
£50000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a leader in advanced material manufacturing, is seeking a highly skilled Senior Quality Control Engineer to join their innovative team in **Newcastle upon Tyne, Tyne and Wear, UK**. This role is integral to ensuring the exceptional quality and reliability of our cutting-edge products. You will be responsible for developing, implementing, and maintaining robust quality control systems and processes throughout the manufacturing lifecycle. This is a hybrid role, offering a blend of in-office collaboration and remote flexibility.
Responsibilities:
Responsibilities:
- Develop, implement, and manage comprehensive quality control plans and procedures for raw materials, in-process production, and finished goods.
- Conduct rigorous testing and analysis of materials and products using advanced metrology equipment and techniques to ensure compliance with specifications and standards.
- Investigate quality deviations, root cause analysis, and implement corrective and preventive actions (CAPA) to resolve issues.
- Collaborate closely with R&D, production, and engineering teams to ensure quality considerations are integrated into new product development and process improvements.
- Monitor key quality metrics, generate detailed reports, and present findings to management and cross-functional teams.
- Oversee the calibration and maintenance of all quality control instrumentation and equipment.
- Ensure compliance with relevant industry standards and regulatory requirements (e.g., ISO 9001).
- Train and mentor junior quality control technicians and engineers.
- Lead quality improvement initiatives and champion a culture of continuous improvement throughout the organization.
- Conduct internal audits and supplier quality assessments as needed.
- Bachelor's degree in Engineering (Mechanical, Materials, Chemical, or related field).
- Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment, preferably in advanced materials.
- Strong knowledge of statistical process control (SPC), Six Sigma, Lean Manufacturing principles, and quality management systems (QMS).
- Proficiency with advanced testing and measurement equipment (e.g., CMM, SEM, spectroscopy).
- Experience with root cause analysis tools and methodologies (e.g., 5 Whys, Fishbone diagrams).
- Excellent analytical, problem-solving, and decision-making skills.
- Strong written and verbal communication skills, with the ability to document findings and present complex information clearly.
- Proficiency in relevant software, including statistical analysis tools and ERP systems.
- Ability to work effectively in a hybrid environment, balancing remote work with essential on-site responsibilities.
- Experience in aerospace, automotive, or medical device manufacturing is a plus.
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3
Quality Control Manager (Manufacturing)
SR1 1PL Sunderland, North East
£48000 Annually
WhatJobs
Posted 8 days ago
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Job Description
Our client, a prominent manufacturing firm, is seeking a dedicated and experienced Quality Control Manager to oversee and enhance its quality assurance processes at their facility in Sunderland, Tyne and Wear, UK . This leadership position requires a strategic thinker with a comprehensive understanding of quality management systems, regulatory compliance, and continuous improvement methodologies. You will be responsible for developing, implementing, and maintaining robust quality control policies and procedures across all production lines. This includes conducting regular audits, analysing quality data, identifying root causes of defects, and implementing corrective and preventive actions (CAPA). The role demands strong leadership skills to manage and mentor a team of quality inspectors and technicians, fostering a culture of quality excellence throughout the organisation. Collaboration with production, engineering, and R&D departments is essential to ensure product quality from design to final delivery. Experience with ISO standards (e.g., ISO 9001) and other relevant industry certifications is crucial. The ideal candidate will possess a Bachelor's degree in Engineering, Quality Management, or a related field, with a minimum of 6 years of experience in quality control within a manufacturing setting, including at least 2 years in a supervisory or managerial capacity. Excellent analytical, problem-solving, and communication skills are a must. This hybrid role offers the opportunity to make a significant impact on product quality and customer satisfaction.
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4
Lead Quality Control Inspector
SR1 2AA Sunderland, North East
£28000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading manufacturing firm based in **Sunderland**, is looking for a highly diligent and experienced Lead Quality Control Inspector. This role is crucial for ensuring that all manufactured products meet stringent quality standards and specifications. You will be responsible for leading a team of QC inspectors, conducting thorough inspections of raw materials, in-process components, and finished goods, and identifying any defects or deviations from quality requirements. The Lead QC Inspector will also be tasked with developing and implementing quality control procedures, maintaining accurate records of inspections and testing, and reporting findings to the Production Manager. You will play a key role in continuous improvement initiatives aimed at enhancing product quality and reducing waste. The ideal candidate will have a strong understanding of manufacturing processes, quality management systems (e.g., ISO 9001), and various inspection techniques. Excellent attention to detail, problem-solving abilities, and strong leadership skills are essential for this position. This is a hands-on role requiring excellent communication skills to liaise effectively with production teams and management.
Key Responsibilities:
Key Responsibilities:
- Lead and supervise a team of Quality Control Inspectors.
- Conduct comprehensive inspections of raw materials, components, and finished products.
- Develop and refine quality control protocols and testing procedures.
- Ensure compliance with all relevant industry standards and regulations.
- Maintain detailed inspection records and generate quality reports.
- Identify and investigate quality issues, implementing corrective actions.
- Collaborate with production and engineering teams to address quality concerns.
- Champion quality improvement initiatives throughout the manufacturing process.
- Train and mentor QC inspectors on best practices and procedures.
- Proven experience in a Quality Control or Quality Assurance role within manufacturing.
- Experience in a leadership or supervisory capacity.
- Strong knowledge of quality management systems (e.g., ISO 9001).
- Proficiency in using inspection tools and equipment.
- Excellent analytical and problem-solving skills.
- High attention to detail and accuracy.
- Good understanding of manufacturing processes.
- Strong communication and interpersonal skills.
- Relevant certifications in quality control are a plus.
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5
Remote Senior Quality Control Inspector
SR1 2AB Sunderland, North East
£38000 Annually
WhatJobs Direct
Posted today
Job Viewed
Job Description
Our client, a rapidly growing manufacturing company, is seeking an experienced and meticulous Remote Senior Quality Control Inspector to join their dedicated team. This is a fully remote position, allowing you to contribute to our quality assurance efforts from the comfort of your home office. The Senior Quality Control Inspector will be responsible for developing, implementing, and overseeing quality control procedures and standards to ensure the consistent production of high-quality manufactured goods.
Responsibilities:
Responsibilities:
- Develop, implement, and refine comprehensive quality control plans and procedures.
- Conduct remote inspections of manufactured products at various stages of the production process, utilizing provided documentation and potentially remote viewing tools.
- Analyze inspection data, identify trends, and report on product quality issues and non-conformances.
- Collaborate with production and engineering teams to address quality defects and implement corrective actions.
- Ensure compliance with internal quality standards, industry regulations, and customer specifications.
- Maintain accurate and organized quality control records and documentation.
- Train and guide junior quality control staff as needed.
- Stay up-to-date with advancements in quality control methodologies and technologies.
- Participate in internal and external audits related to quality management systems.
- Recommend process improvements to enhance product quality and manufacturing efficiency.
- Develop and maintain quality control checklists and inspection criteria.
- Manage the disposition of non-conforming materials.
- Proven experience as a Quality Control Inspector or in a similar quality assurance role within a manufacturing environment.
- Strong understanding of quality control principles, statistical process control (SPC), and quality management systems (e.g., ISO 9001).
- Excellent analytical, problem-solving, and decision-making skills.
- Proficiency in interpreting technical drawings, specifications, and quality standards.
- Strong computer skills, including experience with spreadsheets and databases. Familiarity with remote collaboration tools is essential.
- Excellent attention to detail and accuracy.
- Effective communication and reporting skills, both written and verbal.
- Ability to work independently with minimal supervision and manage time effectively in a remote setting.
- Experience in a senior capacity or with a track record of process improvement is highly desirable.
- Relevant certifications (e.g., ASQ Certified Quality Inspector) are a plus.
- Must be authorized to work in the UK and have a reliable home office setup.
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6
Remote Pharmaceutical Quality Control Analyst
SR1 2AH Sunderland, North East
£40000 Annually
WhatJobs
Posted 5 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to producing high-quality medicines, is seeking a meticulous and dedicated Remote Pharmaceutical Quality Control Analyst to join their expanding team. This crucial role ensures that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements before release. You will be responsible for performing a range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and sophisticated instrumentation. This includes but is not limited to HPLC, GC, UV-Vis spectroscopy, and dissolution testing. Meticulous documentation of all testing procedures, results, and deviations in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is paramount. You will contribute to the investigation of out-of-specification (OOS) results and deviations, working collaboratively with the quality assurance department and manufacturing teams to identify root causes and implement corrective actions. The ability to interpret analytical data and ensure product integrity is essential.
The ideal candidate will possess a degree in Chemistry, Pharmacy, Biology, or a related scientific discipline, with practical laboratory experience in a pharmaceutical or quality control setting. Proficiency with common analytical instrumentation and laboratory techniques is required. A strong understanding of GMP/GLP regulations and quality control principles within the pharmaceutical industry is mandatory. You should have excellent attention to detail, strong problem-solving skills, and the ability to manage your workload effectively in a remote environment. While this role is fully remote, requiring no physical presence at a lab or office, it demands a high level of organisation and self-discipline. You will be provided with necessary resources and clear protocols for remote laboratory work or data analysis. Clear and concise communication skills are vital for reporting results and participating in virtual team discussions. We are looking for an analytical thinker who is committed to maintaining the highest standards of pharmaceutical quality and patient safety. This is an exceptional opportunity to contribute to the production of vital medicines from a remote location, offering flexibility and a chance to be part of a crucial aspect of pharmaceutical manufacturing. The administrative base for coordination is in Sunderland, Tyne and Wear, UK .
Key Responsibilities:
The ideal candidate will possess a degree in Chemistry, Pharmacy, Biology, or a related scientific discipline, with practical laboratory experience in a pharmaceutical or quality control setting. Proficiency with common analytical instrumentation and laboratory techniques is required. A strong understanding of GMP/GLP regulations and quality control principles within the pharmaceutical industry is mandatory. You should have excellent attention to detail, strong problem-solving skills, and the ability to manage your workload effectively in a remote environment. While this role is fully remote, requiring no physical presence at a lab or office, it demands a high level of organisation and self-discipline. You will be provided with necessary resources and clear protocols for remote laboratory work or data analysis. Clear and concise communication skills are vital for reporting results and participating in virtual team discussions. We are looking for an analytical thinker who is committed to maintaining the highest standards of pharmaceutical quality and patient safety. This is an exceptional opportunity to contribute to the production of vital medicines from a remote location, offering flexibility and a chance to be part of a crucial aspect of pharmaceutical manufacturing. The administrative base for coordination is in Sunderland, Tyne and Wear, UK .
Key Responsibilities:
- Perform a variety of analytical tests on raw materials, intermediates, and finished pharmaceutical products.
- Operate and maintain analytical instrumentation (e.g., HPLC, GC, spectrophotometers).
- Accurately document all test results, observations, and deviations according to GMP/GLP.
- Investigate and troubleshoot out-of-specification (OOS) results and deviations.
- Contribute to the validation and qualification of analytical methods and equipment.
- Ensure compliance with all relevant regulatory requirements and company policies.
- Prepare Certificates of Analysis (CoA) and other quality documentation.
- Participate in internal and external audits as required.
- B.Sc. or M.Sc. in Chemistry, Pharmacy, Biochemistry, or a related scientific field.
- Minimum of 3 years of experience in pharmaceutical quality control or analytical laboratory work.
- Proficiency in analytical techniques such as HPLC, GC, Karl Fischer titration, and UV-Vis spectroscopy.
- Thorough understanding of GMP, GLP, and pharmaceutical quality systems.
- Excellent documentation, data interpretation, and problem-solving skills.
- Ability to work independently and manage time effectively in a remote setting.
- Strong attention to detail and commitment to accuracy.
- Effective verbal and written communication skills for remote collaboration.
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7
Remote Senior Quality Control Engineer
SR1 2AA Sunderland, North East
£55000 Annually
WhatJobs
Posted 9 days ago
Job Viewed
Job Description
Our client, a leader in advanced manufacturing, is seeking an experienced Remote Senior Quality Control Engineer to join their dedicated team. This position is critical for ensuring the highest standards of product quality and process integrity throughout the manufacturing lifecycle. You will be responsible for developing, implementing, and overseeing quality control systems and procedures, driving continuous improvement initiatives from your home office.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain comprehensive quality control plans and standard operating procedures (SOPs).
- Design and execute inspection and testing protocols for raw materials, in-process components, and finished goods.
- Analyze quality data, identify root causes of defects, and implement corrective and preventive actions (CAPA).
- Lead and participate in internal and external quality audits.
- Collaborate with engineering, production, and R&D teams to ensure product specifications and quality standards are met.
- Monitor manufacturing processes for adherence to quality standards and identify areas for improvement.
- Develop and deliver quality training programs for manufacturing personnel.
- Manage calibration programs for testing and measurement equipment.
- Stay up-to-date with industry best practices, regulatory requirements, and emerging quality control technologies.
- Prepare detailed quality reports for management review.
- Drive continuous improvement initiatives to enhance product quality, reduce waste, and improve efficiency.
- Bachelor's degree in Engineering (Mechanical, Electrical, Industrial) or a related technical field.
- Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
- Strong understanding of quality management systems (e.g., ISO 9001).
- Proficiency in statistical process control (SPC) and other quality analysis tools.
- Experience with root cause analysis techniques (e.g., 5 Whys, Fishbone diagrams).
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams remotely.
- Detail-oriented with a commitment to accuracy and thoroughness.
- Experience with specific manufacturing processes relevant to the industry (e.g., CNC machining, injection molding, electronics assembly) is a plus.
- Familiarity with quality control software and data analysis tools.
- Must be self-motivated, organized, and able to manage time effectively in a remote work environment.
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8
Senior Pharmaceutical Quality Control Analyst
Sunderland SR1 2AN Sunderland, North East
£40000 Annually
WhatJobs
Posted 15 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly skilled and dedicated Senior Pharmaceutical Quality Control Analyst to join their dynamic team in Sunderland, Tyne and Wear, UK . This pivotal role is responsible for ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis.
The successful candidate will perform a wide range of laboratory tests on raw materials, in-process samples, and finished products using advanced analytical techniques such as HPLC, GC, UV-Vis, and FT-IR spectroscopy. You will be involved in method development, validation, and transfer activities, ensuring compliance with stringent regulatory standards including GMP and ICH guidelines.
Key responsibilities include:
The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific discipline, coupled with at least 5 years of progressive experience in pharmaceutical quality control. A strong understanding of analytical instrumentation and pharmaceutical manufacturing processes is essential. Excellent problem-solving skills, meticulous attention to detail, and the ability to work independently and as part of a team are crucial. This role offers a unique opportunity to contribute to the development and manufacturing of life-saving medicines in a state-of-the-art facility.
The successful candidate will perform a wide range of laboratory tests on raw materials, in-process samples, and finished products using advanced analytical techniques such as HPLC, GC, UV-Vis, and FT-IR spectroscopy. You will be involved in method development, validation, and transfer activities, ensuring compliance with stringent regulatory standards including GMP and ICH guidelines.
Key responsibilities include:
- Conducting comprehensive analytical testing and data interpretation.
- Maintaining detailed and accurate laboratory records in accordance with regulatory requirements.
- Troubleshooting analytical methods and instrumentation, identifying root causes of deviations and implementing corrective actions.
- Participating in internal and external audits, providing necessary documentation and explanations.
- Collaborating with R&D, Production, and Regulatory Affairs departments to resolve quality-related issues.
- Staying abreast of the latest scientific advancements and regulatory updates in pharmaceutical analysis.
- Mentoring junior analysts and contributing to team development.
The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific discipline, coupled with at least 5 years of progressive experience in pharmaceutical quality control. A strong understanding of analytical instrumentation and pharmaceutical manufacturing processes is essential. Excellent problem-solving skills, meticulous attention to detail, and the ability to work independently and as part of a team are crucial. This role offers a unique opportunity to contribute to the development and manufacturing of life-saving medicines in a state-of-the-art facility.
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9