Average salary: €14,544 /yearly
More statsGet new jobs by email
Search Results: 42 vacancies
- ...supervision and guidance of ISL technical and operational teams. Like all SGS personnel, they are committed to upholding stringent technical and GMP standards, ensuring the safety of medications for the multitude of patients relying on the products we test. Due to growth, we have...SuggestedFull timeLocal areaWorldwideFlexible hours
- ...leadership and expertise for automation support of manufacturing operations in accordance with appropriate Good Manufacturing Practices (GMP) and safety guidelines. This leadership role includes mentoring Process Automation Engineers on process control system configuration,...SuggestedFor contractorsWorking Monday to Friday
- ...worksheets, methods and reports (tabular, trend and labels) within the QCL electronic systems. # Supports the Authoring/review of key GMP documents such as GMP standard operating procedures, training materials, test methods creation documents, local qualification documents...SuggestedLocal area
- ...: Bulk API, sterile products, secondary packaging, Devices and to a lesser extent lab projects. ~ Experience in the following areas: GMP manufacturing, LEAN, Automation, construction, construction quality, project controls, the engineering disciplines, safety, scheduling....SuggestedTemporary workFor contractorsFor subcontractorLong term contractLong distanceFlexible hours
- ...skills in MS Excel, Powerpoint & Word. Business acumen with an ability to deliver process improvement objectives Good knowledge of GMP / FDA regulatory requirements, housekeeping, health and safety. Genuine interest in investing in people and facilitates individual...SuggestedFixed term contractShift workWeekend workAfternoon shift
- ...communications skills. ~ Good written and verbal communication skills for both technical and non-technical audiences. ~ Knowledge of GMP, regulatory requirements, computer system validation. ~ Preferable ~ Process Engineering experience. ~ Experience in DCS batch...Suggested
- ...site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup of GMP operations. The QC Systems and Compliance team provides support to the QC function owning cross lab programs such as electronic systems...SuggestedLong term contract
- ...company policies and procedures and will drive improvements in line with regulatory changes (including but not limited to 21 CFR Part 11, EU GMP Annex 11 and Data Integrity Guidance) Provide technical oversight for computerised instrument validation (CSV) processes, in...SuggestedFull time
- ...communications skills. ~ Good written and verbal communication skills for both technical and non-technical audiences. ~ Knowledge of GMP, regulatory requirements, computer system validation. Preferable: ~7 years + as a controls engineer in a highly automated...Suggested
- ...the team’s area of responsibility. Previous supervisory experience desirable Ideally a minimum of 5 years experience within a GLP/GMP analytical laboratory environment within the pharmaceutical or medical device industry. Excellent organisational skills are required...Suggested
- ...Talent Development, Manufacturing Training with a focus on regulated environments. Strong understanding of Good Manufacturing Practices (GMP), regulatory requirements, and compliance training. Proven leadership experience in managing and developing L&D teams at site level....SuggestedLocal areaShift work
£ 43.16 - 51.79 per hour
..., oversee vendor testing, and analyse data. Lead design reviews and recommend optimal sterilisation procedures. Ensure compliance with GMP practices and regulatory standards. Support regulatory documentation and submission processes. The start date is for ASAP. The initial...SuggestedHourly payContract workWork at officeImmediate startRemote work3 days week1 day week- ...experience in machine vision engineering, preferably in regulated high-volume automated manufacturing environments Experience working with GDP/GMP/GAMP standards Proficient with Cognex In-Sight cameras, BCRs, and In-Sight Explorer (spreadsheet programming) Strong knowledge of...SuggestedPermanent employmentFor contractorsRemote workRelocationWorking Monday to Friday
- ...analytical team. This role is key in supporting the development, validation, and routine application of analytical test methods — all within a GMP-compliant environment focused on safety, compliance, and patient-first outcomes. What You’ll Do ✔ Perform analytical testing on...SuggestedContract workWorldwide
€40k - €45k per annum
...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. Essential Qualifications and Experience:...SuggestedFlexible hoursShift workWorking Monday to Friday- ...initiatives. Key Responsibilities: Quality Assurance Oversight: Influence and oversee Commissioning and Qualification (C&Q) of GMP assets including review and approval of associated deliverables (protocols, drawings, test documents, etc.). Develop and maintain...
- ...subject Previous experience in industry desirable Understanding of Med Device concepts desirable. Familiarity with ISO 13485, GDP, GMP concept desirable. Excellent communication skills and attention to detail. Have a good understanding of engineering and quality...Fixed term contract
- ...needed. Validation and Compliance Knowledge. GxP Guidelines : Familiarity with GxP guidelines such as Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), and Good Clinical Practice (GCP). FDA 21 CFR Part 11 : Understanding of the regulatory requirements...Permanent employmentFull time
- ...tools and techniques. Additional Skills: Understanding of pharmaceutical manufacturing industry processes and familiarity with GMP regulations would be an advantage. A high level of intellectual curiosity, external perspective, and innovation interest. Experience...Full time
- ...of quality systems, The self-inspection program, time on the floor program, Verification of the effective implementation of key GMP programs, Review of systems that impact safety, identity, strength, purity, and quality to ensure that they operate in a state of control...Full timeFor contractorsLocal area