Search Results: 66 vacancies
...Excellent opportunity for a QA Specialist with a leading Life Sciences company located in the North West of Ireland . The QA Specialist ensures product manufacturing complies with GMP and Regulatory standards. Responsibilities include validating facility, equipment...
€75k - €90k per annum
Position Summary
The Quality Manager will have overall responsibility for the Quality function, including management of the current Quality Management System.
Responsibilities
The Quality Manager is responsible for:
Ensuring that the processes needed for the Quality...
...LinkedIn .
Job Description
More than a job. It's a chance to make a real difference.
We are now recruiting a Manufacturing QA Compliance Analyst to join our diverse Aseptic Quality team in Westport, Co. Mayo, on a fixed term contract.
This is a shift based...
€50k - €60k per annum
...QA Specialist
Join Our Quality Team!
Job Title: QA Specialist
Department: Quality
Reports to: Quality Manager
Job Purpose: As a QA Specialist, you will play a crucial role in ensuring product quality in compliance with GMP and Regulatory requirements. This individual...
...abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .
Job Description
We are now looking for a Regional QA Systems Lead to join our team on a fixed term contract. Optimise and improve Quality Systems (QS) performance within and across Regional...
...Our client based in Sligo are looking to hire a QA Manufacturing Compliance Specialist on an initial 12 month fixed term contract.
Responsibilities:
Ensure that all products leaving Company XXX meet the standards required for marketed and investigational drug products...
...Our client based in Westport Co Mayo are looking to hire a Manufacturing QA Compliance Analyst to join their diverse Aseptic Quality team in on a 12 month fixed term contract.
This is a shift based role, requiring the successful candidate to work 12 hour rotational shift...
...independently with minimum direct supervision.
* Experience of Pharmaceutical Industry Regulations cGMP/cGLP, 21 CFR 11 and EU Annex 11 compliance requirements.
* Experience working with all disciplines in and supporting a Laboratory environment including QA, CSV, QC, Lab Analysts
...promoting awareness of best industry practices, making appropriate decision on a daily basis utilizing the quality engineering manager/site QA Director as the final arbitrator on critical quality decisions.
Fully conversant with validation techniques and associated regulatory...
...departments across the site, including Manufacturing, Technical Operations, Validation, IT, Site Services, Maintenance, Project Engineering, and QA to ensure that all manufacturing control systems meet global and local compliance requirements, end user requirements, and Quality / IT...
...The position will liaise with Global Engineering (GE), New Product Development (NPD), Research and Development (R&D), Quality Assurance(QA) & Supply Chain(SCM) in order to effectively carry out its responsibilities.
RESPONSIBILTIES:
Key responsibilities of the...
...identifying process improvements. In addition to this, the Automation Engineer will be responsible for working closely with Operations, QA, E&T and Maintenance to drive data integrity requirements for the business units.
Roles and Responsibilities
Primary responsibility...
...excellence and key operations targets, including OEE where applicable
* Provide direct interface as a subject matter expert with the QA department to interact with HPRA, FDA and applicable health authorities and internal audits.
What you need to apply:
* Minimum of 5 years...
...functions across the site, including Validation and IT, Manufacturing, Technical Operations, Site Services and Project Engineering and QA to ensure that all manufacturing and control systems are fit for purpose and meet the global and local compliance, including Quality and...
...ensuring full staffing and appropriate management of constraints or escalation to the TSL.
Ensure all activities align with regulatory (QA & EHS) and corporate requirements.
Lead or participate in Root Cause Analysis of non-conformances, equipment issues, environmental...
...+ (***) ***-****.
Date Posted:
23/04/24 - 15:18 Location:
Galway | Limerick | Midwest | Munster Category:
Electronics | HW Engineer | Test / QA Job Reference:
PBREC/2401 Job Type:
Permanent...
...data analysis techniques by resolving missing/incomplete information in routine assignments.
Administration and Organization of the QA Mailbox including recognizing where escalation points are required.
Compliant distribution – QA approval of Product supporting the interface...
...process.
Requirements:
~ Minimum recognized 3rd level qualification (Certificate/Diploma) in a Science related discipline.
~3 year QA experience in medical device field or equivalent
~ Must possess strong analytical and process skills, and be computer proficient in...
...Ability to work closely with other areas/departments within an organization.
* Good communication and interpersonal skills required to work in a multi-function, matrix team and organisation.
* Experience of H&S, HSA and QA requirements. Proven ability to maintain schedules
...Senior Manufacturing Analyst will communicate regularly with alternate shifts and other Departments such as Microbiology Lab, Maintenance, QA, Contamination Control Operators (CCO’s) and others
Why you should apply:
* This is an excellent opportunity to join a world class...