QA Auditor Job at Bakkavor (London)

Qa Auditor

In this busy and hands-on role as a Quality Auditor, you’ll audit, monitor, and ...

Location

United Kingdom , Sutton Bridge

Salary:

Not provided

Bakkavor

Expiration Date

Until further notice

Requirements

A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment
A proactive, detail-focused approach with a natural curiosity to challenge and improve standards
Confidence working hands-on on the factory floor, providing clear and practical technical guidance
Ability to audit effectively, identify root causes, and drive corrective and preventative actions
Strong communication skills, able to engage confidently with colleagues at all levels
A collaborative mindset, working effectively within cross-functional teams
Good organisational skills, with the ability to manage multiple priorities to deadlines
Commitment to continuous improvement and personal development
A positive, resilient approach aligned to Greencore values

Job Responsibility

Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure
Apply an inquisitive audit mindset to identify root causes and reduce repeat non-conformances
Conduct traceability audits, efficiently retrieving data and presenting findings clearly
Complete sampling activities to schedule, including microbiological, nutritional, swabs, and organoleptic testing
Prepare, facilitate, and trend taste panels, escalating out-of-specification results and recommending improvements
Calibrate factory measurement equipment to schedule and manage out-of-tolerance actions
Support investigations into complaints, incidents, and out-of-specification results through audits and data analysis
Support NPD trials and product launches, including testing, shelf-life assessment, and taste panels
Provide day-to-day technical support to factory teams, audits, and customer visits
Contribute to Technical KPI delivery through audits, investigations, and proactive improvement actions

What we offer

Company share save scheme
Competitive matched pension contribution
Life insurance up to 4x salary
Holidays
Exclusive Greencore employee discount platform
Access to a full Wellbeing Centre platform
Enhanced parental leave and menopause policies

Fulltime

QA Auditor

In this busy and hands-on role as a Quality Auditor, you’ll audit, monitor, and ...

Location

United Kingdom , Boston

Salary:

Not provided

Bakkavor

Expiration Date

Until further notice

Requirements

A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment
A proactive, detail-focused approach with a natural curiosity to challenge and improve standards
Confidence working hands-on on the factory floor, providing clear and practical technical guidance
Ability to audit effectively, identify root causes, and drive corrective and preventative actions
Strong communication skills, able to engage confidently with colleagues at all levels
A collaborative mindset, working effectively within cross-functional teams
Good organisational skills, with the ability to manage multiple priorities to deadlines
Commitment to continuous improvement and personal development
A positive, resilient approach aligned to Greencore values

Job Responsibility

Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure
Apply an inquisitive audit mindset to identify root causes and reduce repeat non-conformances
Conduct traceability audits, efficiently retrieving data and presenting findings clearly
Complete sampling activities to schedule, including microbiological, nutritional, swabs, and organoleptic testing
Prepare, facilitate, and trend taste panels, escalating out-of-specification results and recommending improvements
Calibrate factory measurement equipment to schedule and manage out-of-tolerance actions
Support investigations into complaints, incidents, and out-of-specification results through audits and data analysis
Support NPD trials and product launches, including testing, shelf-life assessment, and taste panels
Provide day-to-day technical support to factory teams, audits, and customer visits
Contribute to Technical KPI delivery through audits, investigations, and proactive improvement actions

What we offer

Competitive salary and job-related benefits
Holidays
Competitive matched pension up contributions
Life insurance up to 4x salary
Company share save scheme
Greencore Qualifications
Exclusive Greencore employee discount platform
Access to a full Wellbeing Centre platform
Enhanced parental leave and menopause policies

Fulltime

QA Auditor

In this busy and hands-on role as a Quality Auditor, you’ll audit, monitor, and ...

Location

United Kingdom , Bourne

Salary:

Not provided

Bakkavor

Expiration Date

Until further notice

Requirements

A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment
A proactive, detail-focused approach with a natural curiosity to challenge and improve standards
Confidence working hands-on on the factory floor, providing clear and practical technical guidance
Ability to audit effectively, identify root causes, and drive corrective and preventative actions
Strong communication skills, able to engage confidently with colleagues at all levels
A collaborative mindset, working effectively within cross-functional teams
Good organisational skills, with the ability to manage multiple priorities to deadlines
Commitment to continuous improvement and personal development
A positive, resilient approach aligned to Greencore values

Job Responsibility

Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure
Apply an inquisitive audit mindset to identify root causes and reduce repeat non-conformances
Conduct traceability audits, efficiently retrieving data and presenting findings clearly
Complete sampling activities to schedule, including microbiological, nutritional, swabs, and organoleptic testing
Prepare, facilitate, and trend taste panels, escalating out-of-specification results and recommending improvements
Calibrate factory measurement equipment to schedule and manage out-of-tolerance actions
Support investigations into complaints, incidents, and out-of-specification results through audits and data analysis
Support NPD trials and product launches, including testing, shelf-life assessment, and taste panels
Provide day-to-day technical support to factory teams, audits, and customer visits
Contribute to Technical KPI delivery through audits, investigations, and proactive improvement actions

What we offer

Company share save scheme
Competitive matched pension contributions
Life insurance up to 4x salary
Holidays
Greencore Qualifications
Exclusive Greencore employee discount platform
Access to a full Wellbeing Centre platform
Enhanced parental leave and menopause policies

Fulltime

QA Auditor Nights

In this busy and hands-on role as a Quality Auditor, you’ll audit, monitor, and ...

Location

United Kingdom , Boston

Salary:

Not provided

Bakkavor

Expiration Date

Until further notice

Requirements

A strong understanding of quality systems, GMP, HACCP, and traceability within a manufacturing environment
A proactive, detail-focused approach with a natural curiosity to challenge and improve standards
Confidence working hands-on on the factory floor, providing clear and practical technical guidance
Ability to audit effectively, identify root causes, and drive corrective and preventative actions
Strong communication skills, able to engage confidently with colleagues at all levels
A collaborative mindset, working effectively within cross-functional teams
Good organisational skills, with the ability to manage multiple priorities to deadlines
Commitment to continuous improvement and personal development
A positive, resilient approach aligned to Greencore values

Job Responsibility

Audit compliance with QMS, GMP, and HACCP, raising clear non-conformances and driving corrective actions to closure
Apply an inquisitive audit mindset to identify root causes and reduce repeat non-conformances
Conduct traceability audits, efficiently retrieving data and presenting findings clearly
Complete sampling activities to schedule, including microbiological, nutritional, swabs, and organoleptic testing
Prepare, facilitate, and trend taste panels, escalating out-of-specification results and recommending improvements
Calibrate factory measurement equipment to schedule and manage out-of-tolerance actions
Support investigations into complaints, incidents, and out-of-specification results through audits and data analysis
Support NPD trials and product launches, including testing, shelf-life assessment, and taste panels
Provide day-to-day technical support to factory teams, audits, and customer visits
Contribute to Technical KPI delivery through audits, investigations, and proactive improvement actions

What we offer

Competitive salary
Holidays
Competitive matched pension up contributions
Life insurance up to 4x salary
Company share save scheme
Greencore Qualifications
Exclusive Greencore employee discount platform
Access to a full Wellbeing Centre platform
Enhanced parental leave and menopause policies

Fulltime

Senior Qa Auditor

We have a fantastic opportunity for a Senior QA Auditor (Wingates) to join our Q...

Location

United Kingdom , Westhoughton

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Previous QA experience within the food industry
Excellent organisation skills
HACCP knowledge

Job Responsibility

Implementing the quality and process audit service to the factories and all associated storage units in order to ensure the objectives and procedures detailed in the quality manual are achieved and to ensure the safety, legality and quality of the product are achieved and maintained
To assist in the operation of the QA function by maintaining satisfactory standards of performance with regard to food safety, hygiene, discipline and health and safety and to bring all the issues arising from these duties to the attention of the Site QA Manager
To complete the daily tasks of the QA in their absence, tasks include: Glass & plastic audits
Foreign body audits
Ingredient shelf-life monitoring
Process checks
Assisting the department in preparation for /factory/SSF in preparing for customer visits/audits
Training and development and performance monitoring of the Quality Auditors
Maintaining satisfactory standards of food safety and hygiene, and to resolve any associated issues, where this is not possible issues are to be brought to the attention of the site Quality Assurance Manager
Management of Yearly Senior QA schedule

Fulltime

Senior QA Auditor

Talentmark are working in partnership with a leading UK life sciences biotechnol...

Location

United Kingdom , London

Salary:

50000.00 - 55000.00 GBP / Year

CK Group

Expiration Date

Until further notice

Requirements

Degree qualified in a relevant scientific subject
GCP for laboratories experience within industry environment i.e. GCLP
Quality assurance auditing and quality system experience within industry
Experience in supporting regulatory inspections and client audits
Proven knowledge of drug development processes
Hold entitlement to work in the UK

Job Responsibility

Supporting with regulatory training, eQMS and QA projects
Ensuring the client are in compliance with the relevant SOPs, regulations and internationally recognised guidelines (GCLP)
Plan and conduct audits of processes, facilities, documents and systems in order to deliver the audit programme as required by GCLP
Assist with Hosting external sponsor audits and regulatory inspections
Act as Lead Auditor to plan, conduct and follow up on-site audits of suppliers and subcontractors
Identify and assess Quality Management System (QMS) non-compliances

Fulltime

Glp/gcp quality compliance auditor

We are seeking an experienced member to join our Quality Assurance team. The Com...

Location

United States of America , Indianapolis

Salary:

Not provided

Labcorp

Expiration Date

Until further notice

Requirements

Bachelor's degree in a Pharmacy, Chemistry or Biology related discipline
Postgraduate degree (MSG or equivalent) in science or management related discipline, preferable
10 years’ experience may be substituted for education
8 years in regulatory environment (experience in GLP/GCP roles)
4 years Laboratory / Quality background specifically with ISO 15189/ISO 13485 standards
Strong written and verbal communication skills
Excellent organizational and project management abilities
Strong negotiation, influencing and networking skills
Demonstrative skills include risk management application experience including risk-based auditing methodologies
Experience in training and developing internal auditors

Job Responsibility

Managing the Internal Audit Program: Plan and implement the internal audit program
Schedule and oversee the approved audit program
Develop and clarify audit scopes to ensure comprehensive assessments
Approve and assign internal audits to appropriate team members
Preparedness and Oversight: Ensure appropriate stakeholder engagement throughout the audit process
Facilitate effective planning and communication with all relevant parties
Audit Hosting & Regulatory Support: Serve as the primary host for internal audits
Provide regulatory inspection support and host sponsor audits as required
Severity Finding and Audit Report Review with Management: Document audit findings and develop detailed reports with actionable recommendations
Collaborate with stakeholders to implement CAPAs and monitor their effectiveness

What we offer

Medical
Dental
Vision
Life
STD/LTD
401(k)
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement
Employee Stock Purchase Plan

Fulltime

Quality Assurance Auditor - Molecular BioA

Labcorp has a Quality Assurance Auditor -Molecular BioA position at 671 South Me...

Location

United States , Greenfield

Salary:

Not provided

Labcorp

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Life Sciences preferred (or equivalent Life Science experience)
3 years in a regulatory environment (experience in GLC/GCP roles)
1 year experience in Molecular BioA
Knowledge of GLP/GCP auditing
Experience with Molecular department specializes in the development, validation, and execution of molecular techniques such as qPCR, RT-qPCR, and Digital PCR, supporting Cell Therapies, Gene Therapies, and Vaccines
Able to influence QA strategy
Knowledge of industry quality systems/standards and able to apply (applicable) regulations to monitor compliance
Experienced in process improvement
Demonstrated ability to apply critical thinking skills
Clear communication skills, including ability to provide clear feedback

Job Responsibility

Conduct inspections in support of GLP or GCP method validation, study-based data and reports
Interpret and apply current policies, procedures and industry guidance in day-to-day auditing
Lead internal study in lab and process/facility inspections
Evaluate and follow up on inspection responses to ensure resolution
Collaborate on quality metrics and identify trends across departments
Review and provide consultation on controlled document revisions
Deliver training related to audit performance
Collaborate with QA teams across sites and contribute to local quality initiatives
Assist in the creation or revision of QA SOPs based on findings and continuous improvement efforts
Organize and manage the workload to meet business needs

What we offer

Medical
Dental
Vision
Life
STD/LTD
401(k)
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement
Employee Stock Purchase Plan

Fulltime

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