Gmp allen jobs in Down 151 -160 of 163 (0.000s)

Cqv site engineer - pharma project

Ballindine

...Review (DR) process and GMP Risk Assessment (FMEA) experience Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP [...]

Category Engineering & Architecture

Senior quality engineer

GalwayCollins McNicholas

...met on time. Maintain GMP standards and compliance in your area. Collaborate with Operations, Supply Chain, and other teams to ensure product and process quality. Lead or participate in Risk Analysis (e.g. FMEA). Review and approve validation protocols, reports (IQ/OQ/PQ), and engineering changes. Maintain documentation in line [...]

Category Engineering & Architecture

Ingénieur qualification validation

Haute-savoieApproach People

...conformité réglementaire (ISO 13485, GMP, 21 CFR Part 11…) Participer aux audits internes/externes et projets transverses Optimiser les pratiques de validation (standardisation, digitalisation)   Profil Bac+5 en ingénierie, procédés, qualité ou équivalent 1ère expérience en qualification/validation (pharma, [...]

Validation engineer

LongfordCollins McNicholas

...SAT protocols. Directly support GMP and regulatory audits. Deliver training and mentor colleagues to strengthen validation knowledge across the business. Perform data analysis to guide informed decision-making and improvements.Requirements: Third-level qualification in Engineering, Polymer Science, or equivalent manufacturing [...]

Category Manufacturing & Production

Qc equipment validation specialist

Cpl

...to ensure compliance with GMP and regulatory requirements. Execute validation protocols, review documentation, and maintain equipment validation lifecycle. Provide technical support and expertise during qualification and validation activities. Ensure adherence to Pfizer standards, quality procedures, and safety [...]

Category Office & Administration

Qc laboratory digital systems specialist

DublinCpl

...Ensure system compliance with cGMP, regulations, and Pfizer standards. Produce regular reports on lab system health (backups, DR, PC status, user practices)Education & Experience Bachelor’s degree in Computer Science, Engineering, or related technical field. Minimum 2 years of IT experience within the pharmaceutical or [...]

Contract Type: Freelance
Category Office & Administration

General operative evening shift

GalwayCpl

...the products in a GMP environment which will be monitored by quality verification.• The individual will also be required to complete documentation to in house standards and be compliant with all in house procedures, i.e. Work Instructions, SOP etc as identified in relevant training plan.• Perform all duties assigned by [...]

Category Management & Consulting

Packaging operator killaloe co. clare

KillaloeCpl

...requirements of ISO 13485, GMP and the Quality Management System• Performs other related duties as assigned.Good rates of pay on offer plus attractive shift allowanceCandidates must have their own transport as there is no public transport in this location.For more information or to apply please email your details to [...]

Category Logistics, Transport & Distribution

Quality specialist

WestmeathCollins McNicholas

...principles and expectations of cGMP regulations. The successful candidate must be able to demonstrable knowledge of HPRA, EU and US GMP/GDP requirements and international guidelines governing pharmaceutical manufacturing and quality systems. This is a permanent opportunity offering hybrid working once [...]

Category Engineering & Architecture

Manufacturing operator

LimerickCpl

...and those elements of GMP deemed necessary to support our business (as outlined in the Quality Manual). Actively complies with and endorses Department and Company objectives. 2. Set-up, process and inspect materials for department operations. Operate,set-up and process machinery. Meet production and ISO 9002, ISO 13485 [...]

Category Manufacturing & Production