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- ...to the Engineering Validation Team Lead, the Senior Engineering Validation Associate will focus on maintaining the validated state of GMP equipment, facilities, utilities, and systems. Responsibilities: Key Subject Matter Expert (SME) in specific validation discipline...SuggestedWorldwideFlexible hours
- ...Responsible for the management and co-ordination of all soft services contractors working under the company's scope in areas including specific GMP equipment/areas and non-GMP equipment/areas. Ensure all PMs and Work Orders are completed on time in a safe and effective manner....SuggestedContract workFor contractors
- ...have experience and understanding of Materials Management in a Biotechnology or Pharma environment with particular focus on maintaining GMP standards. The successful candidate will be an enthusiastic and energetic person with an ability to prioritize & co-ordinate...SuggestedLocal areaWorldwideShift work
- ...implementation Manage traceability in the plant and coordinates required simulation for traceability. Conducts training in Food Safety, GMP in Production, GMP for Maintenance, PRPs etc Draft Manuals & Procedures and Manages Plant Quality Documentation System Coordinates...SuggestedPermanent employment
- ...Working with the general manager, transport manager and purchasing manager to ensure the smooth running of the business. Maintaining GMP / Housekeeping at a high level at all times. Managing process and material flows. Qualifications and Experience: Experience...SuggestedFlexible hoursShift work
- ...expertise, preferably Green Belt Certified or higher •Project management certification, PMP or equivalent. •Strong regulatory and GMP acumen •Detail-oriented, analytical thinker, problem-solver, and able to work in a fast-paced environment. •Proven ability to lead...SuggestedWorldwide
- ...continuous improvement frameworks. ~ Understanding of medical device regulatory and quality standards including FDA, ISO 13485, and GMP. Key Competencies ~ Strategic and analytical mindset with a focus on operational efficiency and long-term business goals. ~...SuggestedLong term contractWorldwide
- ...implementation of appropriate supporting documentation, SOPs, and process work instructions compliant with current Good Manufacturing Practices (GMP) Provision of technical leadership/guidance for the Process/maintenance Technicians and other Manufacturing / Equipment Engineers on...SuggestedPermanent employment
- ...Conduct MSA studies for new products and new processes. ~ Provide training for manufacturing team members. ~ Ensure adherence to GMP and safety procedures. ~ Review and approval of validation documentation. ~ All other duties as assigned. Required Skills...SuggestedFull timeContract workFixed term contract
- ...relevant experience in a team based regulated manufacturing environment, and ideally previous supervisory experience. ~ Good knowledge of GMP / FDA regulatory requirements and current Health and Safety Regulations legislation. ~ Proven experience practicing Lean tools. ~...Suggested
Associate/Senior Associate, IT Systems Business Quality Assurance (BQA), Medicines Quality Orga[...]
...management or statistics. Demonstrated ability to implement, interpret and apply quality systems within a regulated work environment (GMP, GCP, etc.). Demonstrated ability to communicate effectively, both written and verbal, and to influence others. Demonstrated...SuggestedLocal areaHybrid workFlexible hours- ...Plant Deviation Investigations Customer Complaint Investigations Conducting internal compliance audits Reviewing and assessing GMP documentation compliance Providing support to external Customer, Certification and Regulatory audits CAPA and NCR processing...SuggestedLocal area
- ...~ At least 5 years in a managerial or leadership role in a quality-focused function ~ Strong knowledge of cGMP, ICH standards, EU GMP Annexes, and FDA/HPRA requirements. ~ Experience as QP is an advantage For a confidential discussion and more information on the...SuggestedPermanent employmentLocal area
- ...planner ref. adherence to schedule ~Lead and monitor team huddles to ensuring that actions are closed off in a timely fashion ~Drive GMP across the production floor and close off actions as required. ~Manage payroll hours for the team. KEY REQUIREMENTS: ~Strong...SuggestedWorldwideFlexible hoursShift work
- ...own Departmental SOP’s. Review Stores & Inventory levels of critical equipment. Carry out internal audits and periodic reviews of GMP activities to ensure compliance. Develop, review and own relevant SOP’s Support and drive approved initiatives Identify and...SuggestedTemporary workLocal area
- ...Required skills: Bachelor’s degree in engineering or relevant experience. Extensive engineering experience, preferably within a GMP manufacturing environment. Proven project management experience. Strong mechanical skills with hands-on experience in a technical...Contract work
- ...experience of working for a company delivering high value technical solutions to the life sciences industries Good understanding of GMP (Good Manufacturing Practice) Good understanding of Computer System Validation (GAMP V) Good understanding of regulations applicable...Contract workFor contractors
- ...Cooling Towers, Heat Pumps, Air Compressors, WWTP) and HVAC systems including cleanrooms. ~ Familiarity with regulatory requirements, GMP standards and audit experience. ~ Excellent problem-solving, project management, and communication skills. Note: This...For contractorsLocal areaWorldwide
- ...Technology. ~3/4 years’ experience in a manufacturing environment or equivalent with direct experience in a QA environment (preferably GMP regulated). ~ Experience in the medical device industry is an advantage. As a leader in medical science for more than 40 years,...Worldwide
- ...scheduling Organisation skills/Project Management SAP experience desirable Manufacturing Execution Process knowledge Quality and GMP knowledge/experience beneficial Proven excellent communication skills/ communicates effectively Negotiation skills. Proven...
- ...support functions to ensure maintenance requirements are integrated into business planning and execution. Ensure team compliance with GMP, GDP, EHS, and other regulatory and safety requirements. Represent the Maintenance department in cross-functional forums and site-...Full timeFlexible hours
- ...of any position may change over time and may include additional responsibilities not specifically described in the job description. For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding...Contract workLocal areaShift work
- ...with other function leaders where appropriate to ensure the engineering teams comply with and support cross functional best practice in GMP’s, GDP’s, Finance Processes, Compliance Initiatives and EHS Requirements All other duties as assigned. Qualifications Knowledge...Long term contract
- ...be required to perform QA review and approval of packaging and labelling associated documents, procedures, changes, qualifications and GMP deviations. This position requires a sound knowledge of quality assurance systems, methods and procedures. The candidate will be required...Permanent employmentFull timePart timeFor contractorsLocal area
- ...Perform testing of new MES recipes and changes * Generate computer system validation documentation in accordance with site procedures and GMP guidelines * Follow all relevant Environmental, Health and Safety procedures and assist in incident investigations as required. *...Permanent employment
£47.7k - £50.3k per annum
...flexible approach but also able to work under own initiative. * Strong verbal and interpersonal skills Advantage * Experience in a GMP manufacturing environment. * Competent level of technical writing and understanding of technical documentation. Benefits Eirdata...Permanent employmentFor contractorsFor subcontractorFlexible hours- ...Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches. Ensure adherence to GMP and safety procedures. Review and approval of validation documentation. All other duties as assigned. What you will need: B...Permanent employmentContract work
- ...Electronic Change Management Systems & full end-to-end Project Life-cycle. Experience managing cross-functional teams and projects in a GMP Manufacturing Environment. Understanding of Environmental, Health, and Safety requirements of the Pharmaceutical industry. Strong...Contract workImmediate start
- ...Electronic Change Management Systems & full end-to-end Project Life-cycle. ~ Experience in managing cross functional teams and projects in a GMP Manufacturing Environment. ~ Understanding of Environmental, Health and Safety requirements of the Pharmaceutical industry. ~...
- ...involves close collaboration with cross-functional teams and external vendors, with a strong focus on improving equipment uptime in a GMP-regulated manufacturing environment. Responsibilities: # Develop equipment spare parts management system in collaboration with the...For contractors