10 of 10 Permanent GMP Jobs in the North West

validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex 11, and EU GDPR. Supply Chain Responsibilities: • Validate, implement, manage, and maintain an ERP System that is compliant with regulatory requirements in applicable regions ...

validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex 11, and EU GDPR. Supply Chain Responsibilities: • Validate, implement, manage, and maintain an ERP System that is compliant with regulatory requirements in applicable regions ...

validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex 11, and EU GDPR. Supply Chain Responsibilities: • Validate, implement, manage, and maintain an ERP System that is compliant with regulatory requirements in applicable regions ...

completed Collecting micro samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/Fabric audits Temperature checks Quality checks The nature of the role requires a flexible approach to working hours. Core working hours are: Days: Monday ...

fast-paced, ever-changing environment. Strong communication skills. Excellent time management. Desirable skills and experience SQL, R and/or Python coding Experience of GMP rectification and/or equalisation projects Knowledge of the journey through Pensions Risk Transfer transactions Experience providing consultancy services to clients Communicate effectively both verbally ...

with legal, IP, or regulatory teams in a pharmaceutical or consumer healthcare setting. Proven success leading complex cross-functional technical projects. Strong understanding of GMP/GDP and global regulatory requirements. Excellent project management, communication, and stakeholder-management skills. Ability to interpret technical data and legal/contractual documents. Ability ...

with legal, IP, or regulatory teams in a pharmaceutical or consumer healthcare setting. Proven success leading complex cross-functional technical projects. Strong understanding of GMP/GDP and global regulatory requirements. Excellent project management, communication, and stakeholder-management skills. Ability to interpret technical data and legal/contractual documents. Ability ...

with legal, IP, or regulatory teams in a pharmaceutical or consumer healthcare setting. Proven success leading complex cross-functional technical projects. Strong understanding of GMP/GDP and global regulatory requirements. Excellent project management, communication, and stakeholder-management skills. Ability to interpret technical data and legal/contractual documents. Ability ...

with legal, IP, or regulatory teams in a pharmaceutical or consumer healthcare setting. Proven success leading complex cross-functional technical projects. Strong understanding of GMP/GDP and global regulatory requirements. Excellent project management, communication, and stakeholder-management skills. Ability to interpret technical data and legal/contractual documents. Ability ...

with legal, IP, or regulatory teams in a pharmaceutical or consumer healthcare setting. Proven success leading complex cross-functional technical projects. Strong understanding of GMP/GDP and global regulatory requirements. Excellent project management, communication, and stakeholder-management skills. Ability to interpret technical data and legal/contractual documents. Ability ...