Search Results: 364 vacancies
...Senior Computer System Validation Engineer required to Lead Quality, Compliance & CSV by innovative MedTech company in Galway
Responsibilities:
Lead Quality and Compliance activities in relation to Software projects.
Ensure Quality and Compliance with respect to...
...clients are predominantly business owners who are focused on ensuring their day to day operations perform as they should, I.T, networks, systems and cybersecurity are generally not something they have time to consider and that is where we step in. We manage all of the I.T....
...Embedded Systems Engineer
The Embedded Systems Engineer (Firmware & Hardware) role is a new role in a fast growing animal health diagnostics company based in Sligo. You will support both R&D and Operations related activities. As a key member of the team you will participate...
...IT Systems Administrator
Permanent position available with a considerable portfolio of works for the next 5+ years
To build your career by assisting in the delivery of ‘leading edge’ engineering projects.
To work with a vibrant, agile and multi-functional team...
Job title: Senior R&D Engineer – Control system
Location: Parkmore, Galway
Company:
My client are a medical device company developing a new and innovative device to support the heart. Heart support devices are used by interventional cardiologists to stabilize patients...
...itContracting are currently seeking applicants for a Database Systems Administrator. This is a daily-rate contract position located with our client in Galway. Hybrid options available.
Job Description:
Mandatory Requirements:
A degree (NFQ level 7) or higher...
...IT System Installation Engineer - Co. Mayo
My client, one of Europe’s leading innovators in Retail & Hospitality Technology, seeks to hire a motivated IT graduate to work within its Systems division. The successful candidates will be responsible for the Installation and...
£41.1k - £44.6k per annum
...starting materials, finished products and environmental control systems and routine testing where required.
* Responsible for the generation... ...and maintenance of laboratory SOPs and validation documents for GMP lab test procedures and systems.
* Assist in the writing of...
£30k - £42.8k per annum
...Maintain and align with Laboratory Documentation and Computerized Systems Data Integrity requirements.
* Understand Regulations and... ...aseptic processes' manipulation together with experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines....
£ 43 - 56 per hour
...the project lifecycle.
* Provide technical support to all control system related issues. Tasks include, daily trouble shooting,... ...with relevant experience of batch processing and DCS platforms in a GMP environment in the pharmaceutical industry.
* 3 years’ experience...
...implementation of appropriate supporting documentation, which complies with GMP in conjunction with the other team members.
Project planning,... ...and complies with all the regulations governing the quality systems.
Develop themselves and team members.
Qualifications &...
...expertise.
This role will be responsible for ensuring that all systems, facilities, and equipment are installed properly and meet the... ...position will be responsible for supporting project plans aligning with GMP.
What we’re looking for:
~ Bachelor’s degree in Chemical...
...Maintain and align with Laboratory Documentation and Computerized Systems Data Integrity requirements.
* Understand Regulations and... ...aseptic processes' manipulation together with experience within a GLP/GMP environment and knowledge of current EU/FDA/ICH/HPRA guidelines....
£50k - £60k per annum
...the company at client and regulatory meetings and audits.
* Ensure all activities in the department are performed in accordance with GMP, relevant SOP’s and policies.
* Participate in management activities within the operations group to ensure timely and appropriate availability...
...Quality Events Related to the product or process.
Ensure all Quality System documentation is thorough, complete, and compliant.
Audit the... ...is desirable.
~4-5 years’ Experience within a regulated GMP environment is desirable
~1 year plus experience in the day-to-day...
...Production Unit, driving alignment and collaboration across key systems.
Drive Lean initiatives to enhance safety, quality, and customer... ...innovation.
Ensure departmental adherence to regulatory and GMP requirements, promoting quality and customer satisfaction in all...
...exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit... ...out daily tasks as assigned by the Production Manager according to GMP and the quality system
~ Perform activities associated with the...
...the routine maintenance of Quality and other business Management Systems.
Responsibilities:
Possesses and applies a fundamental and... ...Quality Management Systems (e.g. ISO9001/ ISO13485/ ISO14971/ GMP),
Awareness of relevant laws and regulations (e.g. CE/ FDA/ PAL...
...responsible for implementing, maintaining the quality management system, ensuring effective compliance in accordance with regulatory requirements... ...competence.
~ Detailed knowledge of FDA QSR (21 CFR Part 820), GMP, MDSAP, IVDR and ISO 13485.
~ Solid communication and...
...principles.
Work within a highly regulated environment ensuring highest product quality is achieved through robust quality system processes such as GMP, NCR and CAPA etc.
Improve the production flow to achieve quality at source, rapid feedback from inspections....