Search Results: 139 vacancies
...The details for the selected vacancy are shown below.
Advert Text Position Title: GMP Senior Supervisor Location : Client Site Reporting to: Facilities GMP Lead Overall Purpose of the Job Facilities GMP Senior Supervisor will lead and manage the day-to-dayoperations...
...The details for the selected vacancy are shown below.
Advert Text Overall Purpose of the Job GMP Coordinator will play the role to assist in the provision of an efficient and effective cleaningservice in accordance with contractual obligations and company policy and standards...
£ 47 - 51 per hour
...Washers, Autoclaves.
* An understanding of applicable regulations such as Annex 11, GAMP and 21 CFR Part 11.
* 7+ years’ experience in a GMP environment, preferably Pharma/Biopharma.
* Strong problem solving skills.
* Ability to work as part of a wider team.
ADDITIONAL...
£ 21.58 - 27.62 per hour
...semiconductor sub-fab environment.
Proven ability to work safely in industrial environments
Knowledge of Good Manufacturing Practices (GMP) working environment
Strong mechanical aptitude, troubleshooting skills, and or hands-on electrical/electronic experience
Proficient...
£ 43 - 50 per hour
...to be delivered by the projects group. The candidate will have knowledge and proficiency in a variety of areas, most notably HVAC in a GMP space and Isolator HVAC proficiency. Skills should include the use of statistical analysis tools, continuous improvement methodologies,...
...Requirements:
· Bachelor's Degree in Engineering or Relevant Experience
· Typically, 3+ years engineering experience, preferably within a GMP manufacturing environment.
· Strong working knowledge and experience of Site based utilities (HVAC, WIFI, Clean & Black utilities)
·...
...Experience in regulatory audits.
* Working knowledge of biologics analytical methods and specifications and Good Manufacturing Practice (GMP).
* Strong CSV experience with analytical instrument maintenance
* Excellent understanding of data integrity compliance...
...preventive actions, etc.
• Review batch records, both master production/packaging records and executed batch records ensuring compliance with GMP and registration requirements.
• Manage change control requests. This includes, as necessary:
• Process product complaints.
• Review,...
...specific tasks and roles such as: deviation management, change control management, quality systems management, document / SOP management, GMP training & knowledge management.
Ensure the health & wellbeing of the Quality Management system at the site to ensure timely actions...
€ 250 - 350 per day
...communication skills, including technical writing. · MS Excel, MS Word, MS Powerpoint proficiency · Experience of using systems within a GMP environment such as Change Control and Document Management systems.
Job Title: Packaging Engineer
Location: Dublin, Ireland...
€55k - €65k per annum
...relevant experience.
Experience in a pharmaceutical, biotech, medical device, data centre, or health-related facility
Experience in a GMP manufacturing facility and Data Centre's.
Experience in a BMS redundancy design.
Excellent written and verbal communication...
...and IT areas,
Track and provide relevant quality metrics to Quality Management as required,
Perform quality risk assessment of all GMP documentation systems and support stakeholders in the mitigation of compliance risks,
Support the Site Risk management efforts,...
€ 60 - 67 per hour
...implemented timely.
Provide QA review and approval of Change Controls, Deviations/CAPAs, SOPS and related documentation for compliance to GMP and site requirements at the facility.
Provide QA oversight to GMP readiness, technical transfers, regulatory approvals and clinical...
€27 per hour
...controlled plant, handling and packaging equipment, pneumatic and hydraulic components, and control systems
Food safety policies, SOP’s and GMP’s need to be followed and adhered to in maintaining all equipment, to ensure an excellent product is produced.
PPE Gear must be worn...
...to the required specification and that all processes are conducted in line with both good manufacturing practices by conducting regular GMP audits.
~Managing the calibration schedule of key equipment on site.
~Supporting the review and approval of all new product...
...safety policies, procedures, reporting requirements etc
Adhere to all company standards, policies and procedures.
Always maintain GMP standards and good housekeeping
Manage set up of IQMS cards for new employees/card management for existing & leavers
The above...
...to drug product formulation and fill finish operations on site.
The successful candidate will have 4-6 years engineering experience in GMP environment, an understanding of Lean 6 sigma and at least a BSc in Engineering or Scientific discipline.Your main responsibilities...
...Order stock and receive laboratory supplies.
Perform and carry out a variety of routine analytical techniques in compliance with GMP requirements.
Maintain data integrity and ensure compliance with company SOPs specifications and cGMP regulations.
Ensure that...
...such as drug product formulation, vial/pre-filled syringe filling or lyophilisation Qualification in Lean and 6-sigma methodologies would be an advantage. New product introduction (NPI), process development, MSAT experience in a GMP environment would be advantageous. #LI-AP1
€ 78 - 82 per hour
...Project.
Key Responsibilities:
Coordinate and supervise all C&Q activities ensuring adherence to schedule and compliance with GMP and Quality Requirements.
Approve C&Q planning documents and develop master lists of C&Q test documents and activities.
Manage daily...