Search Results: 16 vacancies
...verify that tasks are being performed to the required expectations.
Keeping records in an audit ready state. Ensuring all required GMP and technical documentation is generated and assuring compliance with GMP guidelines and written procedures.
Ability to handle multiple...
Thermo Fisher Scientific Inc.
Athlone, Co. Westmeath
4 days ago
...colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. Our GMP labs in Athlone are continually growing and developing and with that the work is dynamic – projects could include deployment of lab...
Thermo Fisher Scientific Inc.
Athlone, Co. Westmeath
6 hours agonew
...standards.
Working across multifunctional teams and working as a project liaison for vendor and client
Perform IQ,OQ,PQ, FAT's, SAT's, GMP reviews, Risk Assessments, Change Controls, and regulatory auditsAbout you:
Qualification in Engineering, Science, or equivalent Manufacturing...
Longford Town, Co. Longford
6 days ago
...validation, and process.
Review and execution of Factory Acceptance Testing and Site Acceptance Testing protocols.
Directly supports GMP and regulatory audits.
Prepare and deliver training modules as required.
Perform data analysis and make informed decisions /...
Collins McNicholas Recruitment
Longford Town, Co. Longford
22 hours ago
...lieu or degree.
· Experience of multiple laboratory techniques
Desirable Criteria
· Previous relevant industrial experience in a GMP/GLP environment
· Meticulous attention to detail and methodical in review of documents and processes
Additional Criteria...
€74.77k per annum
...within a regulated environment, and ERP/ASCP (SAP preferred)
High understanding of Supply Chain Finance.
Good Manufacturing Processes (GMP)
Experience successfully collaborating with internal and external stakeholders on complex projects.
Further information provided upon...
ECS Resource Group Ltd
Athlone, Co. Westmeath
2 days ago
...deliverables such as process optimization, design verification, stability, packaging and validation qualifications. You will adhere to GMP based Quality Systems requirements for medical devices and medicinal product (e.g. MDD, EU GMP Guidelines Vol IV Part 1 for medicinal product...
...averydennison.com .
Job Description
Supervision of all functions and staff on shift to ensure that all plant Safety, Quality/GMP, Productivity, and Waste management objectives, policies, and procedures are met.
Managing team performance, conducting Technician...
...Relevant Laboratory experience using multiple laboratory techniques.
Desirable Criteria
· Previous relevant industrial experience in a GMP/GLP environment
Additional Criteria information
Please note, we are recruiting for various grades of Analytical Development...
....
Reviews data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP).
Education and Experience
~ Educated to a bachelor's degree level in a relevant area, ie chemistry, biochemistry
In some cases...
Remote job
...relevant quality inspector or QC experience would be an advantage.
~ Knowledge of the Medical Device manufacturing environment including GMP/GDP would be an advantage.
Additional Information
AVERY DENNISON IS EVERYWHERE YOU LOOK:
We not only embrace change…...
...documentation in compliance with STERIS Quality Management System, ISO 11135, ISO 13485 and FDA regulatory requirements while adhering to GMP and GDP requirement.
• Performs according to the guidelines outlined in the STERIS Code of Business Conduct. Supports STERIS AST...
...support within the assigned Customer and/or project teams to ensure Customer and QMS requirements are implemented and fulfilled to required GMP standards.
Lead Quality Engineering activities for the introduction of new product lines through development of product inspection...
...industry experience, may be considered in Lieu of Degree Qualification
· Previous relevant industry experience
· Previous experience in a GMP/GLP environment
· Experience in the performance management of teams
· Up-to-date knowledge of regulatory guidelines relevant to...
...identification and specification review of alternatives and associated implementation efforts
CAPA Management & generation and a dherence to GMP
Communicate project status and escalates issues to direct manager, program managers, internal and external partners in timely...
...and investigated in a timely manner
Ensure Batch records (run files) are competed in full as per Work Instructions and adhering to GMP requirements before transfer to the Quality team for release, ensuring deviations for items are highlighted to the Quality department...
