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- ...regulations pertaining to information security, cyber risk management, compliance, and data privacy (e.g., SOX, GDPR, HIPAA, GxP/GALP/GMP). · Prior experience using an integrated risk management tool (e.g., ServiceNow) and/or vendor risk management tool (e.g., Process Unity...SuggestedPermanent employmentWork at officeFlexible hours
- ...root cause analysis, and the implementation of preventative actions. Maintain documentation and records to meet both regulatory and GMP compliance within a pharmaceutical environment. Participate in and contribute to site safety meetings, risk reviews, and HSE...SuggestedFull timeContract workFor contractors
€66k - €67k per annum
...across the plant. Maintain buildings and utilities systems as needed. Liaise with external contractors and ensure compliance with GMP standards. Manage spare parts inventory and complete maintenance documentation. Criteria National Trade Certificate in a...SuggestedPermanent employmentFor contractorsShift workRotating shiftAfternoon shiftEarly shiftWorking Monday to Friday€70k - €75k per annum
...electrical, and automation systems . Proven track record in project management , team leadership, and regulatory compliance (HACCP, GMP). Excellent problem-solving skills and a continuous improvement mindset . In return, you'll join a forward-thinking company...SuggestedPermanent employment€55k per annum
...in departmental decisions; provide effective solutions for key department stakeholders Knowledge of international standards GLP, and GMP Knowledge of risk-based approach FMEA Must be impartial and work with a sense of urgency Previous QA background in a similar...SuggestedPermanent employment€ 55 - 65 per hour
...projects. Ensure the C&Q activities associated with various capital projects are completed safely, as per schedule and in compliance with GMP and Quality Requirements. Commissioning & Qualification of Clean Utility Systems and execution of qualification documentation...SuggestedHourly payFull timeContract workWork at office3 days week- ...Familiarity with major DCS and working knowledge of BMS/SCADA/PLC systems. Strong customer service, coordination, and interpersonal skills. Good knowledge of GMP regulations. Ability to work across regions, time zones, and travel domestically and internationally....SuggestedWorldwide
- ...validation. Knowledge of control network topologies and signal types (4-20mA, 24VDC, Profibus/Modbus). Experience working in regulated, GMP-compliant facilities. Characteristics We look for candidates who Work well as part of a team. Have excellent problem...SuggestedHourly payContract workFor contractorsLong term contractLocal areaWorldwideFlexible hours
- ...opportunities to enhance MES performance and usability Experience & Skills Required 5+ years' experience delivering MES solutions in GMP life sciences manufacturing, with strong hands-on experience using Emerson Syncade Proven capability in MBR development, recipe...SuggestedHourly payContract workLong term contractLocal areaWorldwideFlexible hours
€ 65 - 75 per hour
...operations and may transition to utilities or cleanroom HVAC roles. Develop and execute commissioning protocols (FAT, SAT, IV, FT) for GMP-regulated systems. Perform system startup, debugging, and initial testing of facility, process, and utility systems. Ensure...SuggestedHourly payFull timeContract workWork at officeRemote workHybrid work- ...needs. ~Positive, proactive attitude with strong work ethic. ~Critical thinking and structured problem-solving ability. ~Knowledge of GMP, EHS standards, and lean manufacturing principles. ~Collaborative team player with effective communication skills at all levels. ~...SuggestedPermanent employmentFull timeFor contractorsFlexible hoursShift work
- ...the wider Engineering group. The successful candidate will have prior relevant facility engineering experience, preferably gained in a GMP manufacturing setting, with experience providing support to the Facility and Utility Support functions. Responsibilities: Collaboration...SuggestedPermanent employment
- ...Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Lab Manager – Biopharma At PPD, part of Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive...SuggestedLong term contractWork at officeRelocationWorking Monday to Friday
- ...qualification in mechatronics, automation or business/management would be advantageous. At least 5 years’ experience in a similar role in a GMP-regulated manufacturing environment; technical team leadership. Strong exposure to process equipment best-practice maintenance...SuggestedFull timeWorldwide
- ...to provide evidence of delivering a number of projects in this technology during your career. A minimum of 5 years experience in a GMP regulated environment (Pharma/Life Sciences, Biotech or Medical Devices) is essential and only candidates with significant experience in...SuggestedPermanent employmentFor contractorsRemote workHybrid work
- ...for internal and external projects (2) independent oversight of commercial manufacture in compliance with Good Manufacturing Practice (GMP) requirements (3) executing Quality Management System requirements in support of commercial and developmental programs (4) ensuring the...Local areaHybrid workFlexible hours
- ...Experience working in pharmaceutical, life sciences, or chemical manufacturing industries. Knowledge of transportation logistics, GMP/GXP standards, and regulatory compliance. Experience with planning systems (e.g., Kinaxis RapidResponse), ERP systems (Oracle EBS, SAP...For contractors
- ...work instructions, and standard operating procedures. Skills and Education: A level 6 with a minimum of 3+ years’ experience in a GMP Manufacturing requirement shall be deemed equivalent. Competent in troubleshooting and show practical problem-solving capabilities....Contract workWorldwideShift work
- ...manuals for clients. Qualifications Requirements: Degree in Mechanical or Chemical Engineering. Knowledge of pharma norms, GMP, GAMP, ASME BPE. Familiarity with pharma utilities like softening, reverse osmosis, electrodeionisation, etc. Understanding of...Contract workWork at officeFlexible hours
- ...deviations and periodic reviews and Data integrity for CSCI • Provide support with guidelines and regulations such as GAMP 5, EU GMP Annex 11, and FDA CFR Part 11 • Act according to the Quality Assurance (QA) vision, strategy and standards for the integrated Perrigo...Work at officeRemote workWork from homeHybrid work2 days week
- ...for the execution of the day-to-day tasks as per requirements. Duties of the Role include; Monitoring relevant control systems for GMP and Non GMP alarms. Responsible for escalation of alarms in accordance with relevant escalation procedures and SOP’s....Permanent employmentFull timeContract workFor contractorsHybrid work
- ...strategy to ensure that the validation approach satisfies the requirements of all regulatory bodies; regulations, standards, guidance and GMP, including effective and appropriate use of process development and DOE activities Produce and maintain appropriate and...
- ...The FLM is responsible for effective management of a shift of Process Technicians to achieve production targets efficiently in line with GMP, safety and other regulatory standards. The FLM facilitates daily scheduling and work centre team meetings ensuring that all groups...Shift work
- ...Ensuring all the operating systems are in compliance with all Regulatory and Legal requirements including, EPA licence, Quality (cGDP/GMP’s), EHS, Global Engineering, design & construction directives, requirements & procedures. Key requirements include: Requires extensive...Contract work
- ...statistical analysis to drive decision making (e.g. SPC trending, Nelson/WACO trend rules, process capability, etc) Preferred Experience ~ GMP experience including regulatory agency audits ~ Proficiency in the basic operation and automation configuration associated with...Full time
- ...contract labs, excipient suppliers, commodity suppliers, medical devices, logistic providers, and third-party manufacturers. Your work in GMP compliance and quality will ensure that activities are performed and documented in accordance with AbbVie policies, procedures, and...Contract work
€30.4k per annum
...timely delivery. Collaborate closely with the Quality department on quality-related issues, including maintaining and developing GMP within the manufacturing area. Follow standard operating procedures and good manufacturing practices strictly to ensure...WorldwideShift workNight shiftWorking Monday to Friday- ...and food safety matters to departments including Production and Maintenance. Manage internal auditing systems to uphold hygiene and GMP standards, ensuring timely corrective action where needed. Trend and analyse QA data (e.g. lab results, complaints, audit outcomes)...Permanent employmentFull time
- ...able to provide evidence of delivering a number of projects in this technology during your career. A minimum of 5 years experience in a GMP regulated environment (Pharma/Life Sciences, Biotech or Medical Devices) is essential and only candidates with significant experience...Permanent employmentFor contractorsRemote work
€90k per annum
...standards and have the required functionality. Requirements: A minimum of five years' experience working in a similar role. GMP regulated environment or Facilities Management experience. Project Management in Construction/client side. Managing projects in a...Permanent employmentWorking Monday to Friday