1 to 25 of 55 Permanent GMP Jobs with Remote Work Options

Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

promoted internally. We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who has previous regional experience with some auditing experience. The role is based from more »

have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »

to detail and flexibility. Strong communication skills. Ability to handle stressful situations and controversial issues. Willingness to learn and develop new skills. Knowledge of GMP, GDPR, LSAS, and ethical trade issues. Key Tasks: Prepare and submit regulatory documentation for market registration. Support root cause identification and solution resolution. Conduct and 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 »

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 »

to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions more »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

similar role. Paid, owned, website, & commerce data experience. Strong knowledge of key digital platforms, CRM, data and web analytics providers, including Adobe Marketing Cloud, GMP, GCP, Meta and other partners. Strong knowledge of data management, analytics with experience of deploying data & analytics projects across large accounts. Have managed multi- million more »

s products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide internal consultancy for quality compliance implementation and FDA/EU GMP/GDP remediation projects in the Dechra Internal Manufacturing network. Frequent global travel is required with this role. Main Responsibilities So, what will you be … manufacturing network (as required) across the product's registered lifecycle in compliance with all applicable ISO, ICH, FDA, EU, and national regulatory requirements for GMP/GDP. Lead GMP/GDP audits for Dechra DPMS based on specific expertise, criticality, and complexity. Periodically assess the liability, regulatory and/or … networks are all being adequately monitored. Recruit, lead, train and develop, as required, the team of quality and compliance experts (specialised in auditing different GMP/GDP areas) across the business, to keep the business abreast of ongoing developments through benchmarking activities, whilst proactively identifying and addressing any gaps relating more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »