Showing 40 Bakkavor jobs in Grantham
Automotive Quality Control Inspector
Posted 1 day ago
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Senior Quality Control Engineer
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Key responsibilities include:
- Developing and implementing comprehensive quality control plans and procedures for raw materials, in-process components, and finished goods.
- Conducting regular inspections, testing, and audits to verify product conformity to specifications.
- Investigating quality deviations, identifying root causes, and implementing effective corrective and preventive actions (CAPA).
- Analyzing quality data to identify trends, patterns, and areas for continuous improvement.
- Collaborating with production, engineering, and R&D teams to resolve quality issues and enhance product design.
- Ensuring compliance with relevant industry standards and regulatory requirements (e.g., ISO 9001).
- Maintaining accurate quality records and documentation.
- Leading and mentoring junior quality control staff.
- Developing and delivering quality awareness training to production personnel.
- Recommending process improvements to enhance product quality and reduce waste.
The ideal candidate will possess:
- A Bachelor's degree in Engineering, Science, or a related technical field.
- A minimum of 5 years of experience in a quality control or quality assurance role within a manufacturing environment.
- Proven experience with various inspection and testing methodologies.
- Strong knowledge of statistical process control (SPC) and quality management systems (QMS).
- Familiarity with lean manufacturing principles and Six Sigma methodologies is advantageous.
- Excellent analytical, problem-solving, and decision-making skills.
- Proficiency in data analysis software (e.g., Excel, Minitab).
- Strong communication and interpersonal skills, with the ability to work effectively across departments.
- Attention to detail and a commitment to maintaining high-quality standards.
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Senior Quality Control Inspector
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Senior Quality Control Manager
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Responsibilities:
- Develop and implement comprehensive quality control strategies and procedures across all production lines.
- Oversee the daily operations of the quality control department, including inspection, testing, and documentation.
- Ensure compliance with relevant industry standards (e.g., ISO 9001) and regulatory requirements.
- Conduct internal audits and facilitate external audits by regulatory bodies and customers.
- Analyze quality data, identify trends, and implement corrective and preventative actions (CAPA) to address non-conformities.
- Manage and mentor a team of quality control inspectors and technicians, fostering a culture of quality awareness.
- Collaborate with production, engineering, and R&D teams to resolve quality issues and improve product consistency.
- Manage supplier quality, including evaluation and auditing of raw material suppliers.
- Stay abreast of new quality control technologies and methodologies, recommending improvements.
- Prepare detailed reports on quality performance, metrics, and improvement initiatives.
Qualifications:
- Bachelor's degree in Engineering, Science, or a related technical field.
- Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
- Proven experience with quality management systems (QMS) and standards such as ISO 9001.
- Strong knowledge of statistical process control (SPC), Six Sigma, or other quality improvement tools.
- Excellent analytical, problem-solving, and decision-making skills.
- Effective leadership and team management abilities.
- Proficiency in quality control software and Microsoft Office Suite.
- Strong communication and interpersonal skills, with the ability to influence stakeholders at all levels.
- Detail-oriented and committed to achieving the highest standards of quality.
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Senior Quality Control Inspector
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Responsibilities:
- Perform detailed inspections of raw materials, in-process components, and finished goods to ensure compliance with quality standards and specifications.
- Utilize a range of measurement and testing equipment, including calipers, micrometers, gauges, and CMMs, to verify product dimensions and tolerances.
- Identify and document non-conforming products, initiating corrective actions and quarantine procedures.
- Analyze quality data and trends to identify root causes of defects and implement preventive measures.
- Collaborate with production, engineering, and other departments to resolve quality issues and improve processes.
- Develop and implement quality control procedures and standards.
- Conduct internal audits to ensure adherence to quality management systems (e.g., ISO 9001).
- Prepare detailed quality inspection reports and maintain accurate records.
- Train and mentor junior quality control staff on inspection techniques and procedures.
- Ensure all quality control activities are conducted in a safe and efficient manner.
- Participate in continuous improvement initiatives to enhance product quality and reduce waste.
- Stay current with industry standards and best practices in quality control.
- Proven experience as a Quality Control Inspector or similar role in a manufacturing environment.
- Proficiency in using various inspection tools and equipment, including CMM operation.
- Strong understanding of quality management systems (e.g., ISO 9001) and manufacturing processes.
- Excellent attention to detail and accuracy.
- Ability to read and interpret technical drawings, blueprints, and specifications.
- Good analytical and problem-solving skills.
- Effective communication and interpersonal skills for collaboration.
- Experience in training or supervising junior staff is advantageous.
- A methodical and organized approach to work.
- Basic computer proficiency for data entry and reporting.
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Senior Pharmaceutical Quality Control Analyst
Posted 2 days ago
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Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, IR spectroscopy).
- Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH, FDA, EMA).
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventative actions (CAPAs).
- Prepare and review analytical documentation, including test methods, validation reports, certificates of analysis, and batch release documentation.
- Operate and maintain laboratory equipment, ensuring calibration and performance are within specifications.
- Adhere strictly to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Collaborate with R&D, production, and regulatory affairs departments to resolve quality-related issues.
- Stay up-to-date with current industry trends, scientific advancements, and regulatory updates impacting pharmaceutical quality control.
- Mentor and train junior analysts, sharing expertise and promoting best practices.
- Contribute to the continuous improvement of quality systems and laboratory operations.
- BSc/MSc in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 5 years of experience in pharmaceutical quality control or a related analytical role within the pharmaceutical industry.
- Extensive hands-on experience with various analytical instrumentation (HPLC, GC, dissolution apparatus, etc.) and compendial methods.
- Strong understanding of GMP, GLP, and relevant regulatory guidelines.
- Proficiency in data analysis, interpretation, and scientific report writing.
- Excellent attention to detail, problem-solving abilities, and a meticulous approach to laboratory work.
- Effective communication and interpersonal skills, with the ability to work collaboratively in a team environment.
- Flexibility to work on-site in **Nottingham, Nottinghamshire, UK**, with potential for some remote work activities.
- Experience with statistical software and analytical method validation is highly desirable.
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Remote Quality Control Inspector - Sanitation
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- Conducting comprehensive remote inspections of sanitation processes and documentation using provided digital tools and platforms.
- Analyzing inspection reports, photographic evidence, and data logs submitted by on-site personnel to assess compliance.
- Identifying non-compliance issues, potential risks, and areas for improvement within sanitation practices.
- Developing detailed findings reports, including root cause analysis and actionable recommendations for corrective measures.
- Collaborating with site managers and operational teams via video conferencing and digital communication channels to discuss inspection outcomes and facilitate the implementation of improvements.
- Staying up-to-date with the latest industry best practices, regulations, and standards related to sanitation and hygiene in diverse environments.
- Maintaining accurate and organized records of all inspections, findings, and follow-up actions within the company's quality management system.
- Providing guidance and support to on-site teams on best practices for maintaining high standards of cleanliness and sanitation.
- Participating in virtual training sessions and team meetings to share insights and enhance quality control strategies.
- Contributing to the continuous improvement of sanitation protocols and inspection methodologies.
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Senior Pharmaceutical Quality Control Analyst
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Senior Quality Control Inspector (Remote)
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Responsibilities:
- Develop, implement, and maintain robust quality control procedures and documentation for all manufactured products.
- Conduct thorough inspections and testing of raw materials, in-process materials, and finished goods to ensure compliance with specifications.
- Analyse quality data and generate reports to identify trends, root causes of defects, and areas for process improvement.
- Collaborate with production teams to address quality issues promptly and implement corrective and preventative actions (CAPAs).
- Train and mentor junior quality control personnel on inspection techniques, quality standards, and best practices.
- Stay updated on industry quality standards, regulations, and best practices, and ensure the company's adherence to them.
- Manage calibration and maintenance schedules for all quality control equipment.
- Participate in internal and external audits to ensure compliance with quality management systems (e.g., ISO 9001).
- Contribute to the continuous improvement of quality processes and product consistency.
- Maintain accurate records of all quality-related activities, including inspections, tests, and non-conformance reports.
- Bachelor's degree in Engineering, Quality Management, or a related technical field.
- Minimum of 4-6 years of experience in a quality control or quality assurance role within a manufacturing setting.
- Proven experience in developing and implementing quality control plans and procedures.
- Familiarity with various inspection tools and techniques, including statistical process control (SPC).
- Strong understanding of quality management systems (e.g., ISO 9001, AS9100).
- Excellent analytical, problem-solving, and decision-making skills.
- Exceptional attention to detail and accuracy.
- Proficiency in using quality management software and Microsoft Office Suite.
- Strong communication and interpersonal skills, with the ability to collaborate effectively with remote teams.
- Self-motivated and able to work independently with minimal supervision in a remote capacity.
Location: This role is fully remote, supporting operations relevant to Nottingham, Nottinghamshire, UK .
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Senior Pharmaceutical Quality Control Analyst
Posted today
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Key Responsibilities:
- Perform a variety 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 regulatory guidelines.
- Operate, calibrate, and maintain laboratory instrumentation, ensuring accuracy and reliability.
- Prepare reagents, standards, and samples for analysis.
- Accurately record and report test results, maintaining detailed laboratory notebooks and documentation.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
- Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory requirements.
- Participate in internal and external audits, providing necessary documentation and support.
- Assist in the training and mentoring of junior Quality Control Analysts.
- Contribute to process improvement initiatives within the Quality Control department.
- Maintain a safe working environment in the laboratory.
Qualifications:
- Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 5 years of experience in a pharmaceutical Quality Control laboratory setting.
- Proven experience with analytical techniques such as HPLC, GC, and spectroscopic methods.
- Strong understanding of GMP, ICH guidelines, and other relevant pharmaceutical regulations.
- Experience with method validation and qualification is essential.
- Proficiency in laboratory information management systems (LIMS) is a plus.
- Excellent attention to detail, accuracy, and organisational skills.
- Strong problem-solving and critical thinking abilities.
- Effective communication and teamwork skills.
- Ability to work independently and manage multiple tasks efficiently.
This on-site position offers the opportunity to contribute to vital pharmaceutical quality assurance in Nottingham, Nottinghamshire, UK .
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