13 Manufacturing Companies jobs in Lanchester
Quality Control Manager (Manufacturing)
SR1 1PL Sunderland, North East
£48000 Annually
WhatJobs
Posted 6 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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0
Lead Quality Control Inspector
SR1 2AA Sunderland, North East
£28000 Annually
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Posted 18 days ago
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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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1
Remote Pharmaceutical Quality Control Analyst
SR1 2AH Sunderland, North East
£40000 Annually
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Posted 3 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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2
Remote Senior Quality Control Engineer
SR1 2AA Sunderland, North East
£55000 Annually
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Posted 7 days ago
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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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3
Senior Pharmaceutical Quality Control Analyst
Sunderland SR1 2AN Sunderland, North East
£40000 Annually
WhatJobs
Posted 14 days ago
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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.
This advertiser has chosen not to accept applicants from your region.
4
Senior Pharmaceutical Quality Control Scientist
SR1 2SH Sunderland, North East
£50000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company renowned for its commitment to innovation and quality, is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Scientist. This role is crucial for ensuring the integrity and compliance of pharmaceutical products through rigorous testing and analysis. You will be instrumental in developing, validating, and executing analytical methods, managing laboratory operations, and contributing to regulatory submissions. This is a key position within a state-of-the-art facility dedicated to advancing healthcare solutions.
Key Responsibilities:
Key Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various instrumental techniques (e.g., HPLC, GC, MS, UV-Vis).
- Develop, validate, and transfer analytical methods in accordance with regulatory guidelines (ICH, FDA, EMA).
- Troubleshoot and maintain laboratory instrumentation, ensuring optimal performance and calibration.
- Review and approve analytical data, ensuring accuracy, completeness, and compliance with specifications.
- Write and revise Standard Operating Procedures (SOPs), test methods, and validation protocols.
- Participate in internal and external audits, providing necessary documentation and support.
- Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPA).
- Contribute to the improvement of quality control processes and laboratory efficiency.
- Mentor and train junior QC analysts on technical procedures and compliance requirements.
- MSc or Ph.D. in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 5 years of hands-on experience in pharmaceutical quality control or analytical development.
- Extensive knowledge of analytical techniques such as HPLC, GC, MS, dissolution testing, and spectroscopy.
- Familiarity with GMP (Good Manufacturing Practice) regulations and ICH guidelines.
- Experience in method validation and analytical troubleshooting.
- Strong understanding of pharmaceutical manufacturing processes.
- Excellent data interpretation, problem-solving, and documentation skills.
- Effective communication and interpersonal abilities.
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5
Senior Pharmaceutical Quality Control Analyst
DH1 3NP Sunderland, North East
£30000 Annually
WhatJobs
Posted 14 days ago
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Job Description
Our client, a leading pharmaceutical company based near Sunderland, Tyne and Wear, UK , is looking for a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join their dedicated Quality Assurance department. This role is crucial in ensuring the safety, efficacy, and quality of pharmaceutical products through rigorous testing and analysis. You will be working within a state-of-the-art laboratory environment, contributing to vital drug development and manufacturing processes. The hybrid nature of this role allows for a balance between essential in-lab work and remote administrative tasks.
Responsibilities:
Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using sophisticated laboratory equipment (e.g., HPLC, GC, UV-Vis, FTIR).
- Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH, FDA, EMA).
- Interpret test results, document findings accurately in laboratory notebooks and reports, and identify any deviations or out-of-specification (OOS) results.
- Investigate OOS results, identify root causes, and propose corrective and preventative actions (CAPAs).
- Maintain laboratory equipment, ensuring proper calibration, qualification, and preventative maintenance.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards.
- Prepare analytical reports, specifications, and other quality control documentation.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to support product development and lifecycle management.
- Train and mentor junior QC analysts, providing guidance on analytical techniques and quality standards.
- Contribute to continuous improvement initiatives within the QC department.
- A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline.
- Minimum of 5 years of experience working in a pharmaceutical Quality Control laboratory setting.
- Proven experience with various analytical techniques, particularly HPLC, GC, and dissolution testing.
- Thorough understanding of GMP, GLP, and pharmaceutical regulatory requirements.
- Experience in method development and validation is highly desirable.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong documentation skills with meticulous attention to detail.
- Proficiency in using laboratory information management systems (LIMS).
- Ability to work effectively both independently and as part of a team.
- Good communication skills, with the ability to convey technical information clearly.
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6
Senior Pharmaceutical Quality Control Analyst
SR2 9LY Sunderland, North East
£45000 Annually
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Posted 18 days ago
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Job Description
Our client is seeking a highly experienced Senior Pharmaceutical Quality Control Analyst to join their dynamic, fully remote team. This critical role involves overseeing and executing a range of analytical testing to ensure the quality, safety, and efficacy of pharmaceutical products. The ideal candidate will possess a deep understanding of Good Manufacturing Practices (GMP) and regulatory requirements within the pharmaceutical industry. Responsibilities include developing, validating, and implementing analytical methods; performing complex analytical testing using techniques such as HPLC, GC, UV-Vis spectroscopy, and dissolution testing; reviewing and approving test data and reports; investigating out-of-specification (OOS) results and deviations; authoring and revising Standard Operating Procedures (SOPs); and collaborating with cross-functional teams, including R&D, manufacturing, and regulatory affairs. This position offers the unique opportunity to work from anywhere in the UK, contributing to groundbreaking pharmaceutical advancements. Candidates must demonstrate exceptional attention to detail, strong problem-solving skills, and excellent written and verbal communication abilities. A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field, coupled with a minimum of 5 years of progressive experience in pharmaceutical quality control, is essential. Experience with data integrity principles and regulatory inspections is also highly valued. This is a remote-first position, requiring self-motivation, discipline, and the ability to work independently while maintaining high standards of quality and compliance. Embrace the future of pharmaceutical quality control in a flexible, remote work environment. The successful applicant will play a pivotal role in ensuring our products meet the highest global standards. Key areas of focus will include raw material testing, in-process controls, and finished product release testing. Familiarity with statistical analysis software and quality management systems is also beneficial. This role is crucial for maintaining our stringent quality benchmarks and contributing to patient safety through rigorous analytical oversight. The ability to mentor junior analysts and provide technical guidance will be an advantage.
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7
Senior Pharmaceutical Quality Control Manager
NE6 1AA Newcastle upon Tyne, North East
£75000 Annually
WhatJobs
Posted 22 days ago
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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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8
Senior Pharmaceutical Quality Control Analyst
NE1 1 Newcastle upon Tyne, North East
£45000 Annually
WhatJobs
Posted 23 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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