51 to 75 of 201 Permanent GMP Jobs

site & escalate/action where necessary Working as a support function to operations to ensure hygiene levels of the facility are maintained by conducting GMP/Glass and Hard Plastic and Fabrication audits Carrying out sampling and swabbing & leading on investigations corrections -preventative procedures To be the subject matter expert more »

least 3 years industrial experience and be able to work on a number of product development projects. Previous industrial experience within a regulated environment GMP environment, pharmaceuticals, food, electronics . Demonstrate project control, with evidence on how you achieved the business goal. Provide support to design operatives to aid in more »

work environment and that all tools are maintained and accounted for. Liaise with the SHEQ team to resolve H&S issues, environmental, internal audits, GMP, COSHH and ISO quality issues, and ensure all compliance checks are complete and correctly filled. Attend all nominated training modules as necessary. Undertaking any other more »

area highlighting any stock issues to the engineering team manager To maintain standards of hygiene and good housekeeping appropriate to a quality food manufacturer. GMP standard of workshops and engineers tool boxes is maintained at a high level About you. Strong people management experience A multi skilled background Experience completing more »

facilitate change. The ability to present information coherently, accurately and persuasively. PC literate Experience within food manufacturing, advanced Food Hygiene Certificate & good understanding of GMP/hygiene standards What you'll receive. As an equal opportunity employer, we're committed to providing a safe and rewarding environment for you to more »

part of the process. Engage regularly with multi disciplined teams/training and mentoring. Worked within an Automotive/Pharmaceutical/Medical device/GMP environment. Bachelors degree or equivalent in Engineering. DMAIC (desirable). Lean/Six Sigma qualifications. Travel requirements; Travel between local manufacturing sites is required – no more »

for scaling up and down of bioprocess operations. - Understanding of how to develop and optimise processes for the purification of biopharmaceutical products. - Understanding of GMP and QbD considerations in a large scale manufacturing environment. - Understanding and experience with statistical and modelling software and tools. - Understanding of in-process assays such more »

I am currently supporting a CDMO based in Sawston that provide GMP manufacturing of ATMP's and related products, process development and ancillary services in their search for a Validation Manager. In this role you will be responsible for leading validation, qualification and verification of manufacturing equipment, facilities and lab more »

team members on best practices and ensure compliance with regulatory standards. Conduct gap analysis, review change controls, and develop revalidation strategies as needed. Ensure GMP, Data Integrity, and GDP compliance, including timely training. Key Competencies: Proven track record in delivering regulatory-compliant validation strategies. Strong understanding of GxP compliance requirements. more »

as part of the remuneration. Experience: Experienced project engineer or project manager in a pharmaceutical setting A strong understanding and hands on experience of GMP Engineering or validation experience is essential Exposure to the full validation lifecycle and the ability to walk through the full CQV phase Hands on experience more »

Facilitate flow of information with Quality and Finance departments. Supporting the Supply Chain and Operations to enable that all assets, processes and procedures meet GMP/GDP requirements. Maintain a complete understanding of the flow to ensure an efficient process. Be able to translate forecasts into production schedules, batch allocations more »

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

also possess previous experience in: Post Market Surveillance requirements Using Salesforce Functional knowledge of Quality, Regulatory Compliance, and operations systems and processes to include GMP and QSR requirements for medical devices. (ISO 13485, FDA's QSRs, EU's MDD, Canadian Regulations) is required. Cepheid, a Danaher operating company, offers a more »

Middlesbrough area. Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC more »