Our client a major international Pharmaceutical company, with operations in a multitude of countries across the globe, is looking to recruit a Technical Services Manager to support operations within Ireland.
As a result of excellent progression that our client has seen from their current staff. We are recruiting for a Qualified Person with Sterile manufacturing experience to come into the Quality subject matter expert group.
The quality manager will be a senior leader reporting in to the corporate head of quality. Full authority will be placed on the successful applicant to deliver the quality strategy, this includes management of all quality systems and ensuring GMP compliance is upheld.
This company is a world leader in its industry and value experienced individuals. Due to ongoing expansion and development in their business they are now looking to hire an Development Technologist. This position will be responsible for ensuring major milestone targets are visible for team members and key stakeholders to achieve on time market entry.
An exciting vacancy has arisen for a QA Leader for a Drug Product site in Dublin. This position is a new role in a newly built manufacturing site that will also take responsibility for QP / Batch release for the site. Contact Mark Tierney from Clarity Recruitment on +353 1 5673123 to discuss in confidence.
Our client is seeking a QA Manager for an exciting quality programme they are about to embark on. The QA Manager has full responsibility for the quality management and oversight of sites within their product product portfolio.
Our client is seeking a QA Manager for an exciting project. This discreet project will involve working with a large global consultancy that has a presence in 13 countries and a staff of 700 people working across the world.
This QA Specialist is responsible for supporting the quality management and oversight of CMO’s, as well as, being responsible for identification and escalation of any adverse trends to the appropriate level of management.
The Quality Services and Improvement Manager is responsible for defining the strategic direction of the Quality Department, particularly focusing on Continuous Improvement and Quality Culture activities.
A leading pharmaceutical company is looking for a CSV engineering professional for a 3 month minimum, contract opportunity. This individual will be located onsite 1 day a week while operating from home the remaining 4 days.
Our client is looking to employ a Senior Supply Chain Planner who will be responsible for the procurement and inventory management activities of a top 20 global pharmaceutical company. This Senior Supply Chain person will also play a role in communication on product availability between Manufacturing, Distribution, Customer Service and other relevant stakeholders.
This manager will work closely with all quality personnel and while reporting to the Site Head of Quality (HOQ) will be responsible for overseeing all GMP Quality Systems on site and ensuring compliance to cGMP for all manufactured products: API, biologics and oral solid dosage product. Moreover, the manager will be expected to promote regulatory compliance, as well as, a continuous improvement culture within the site.
The Quality Assurance (QA) Manager will be responsible for assisting in the oversight of cGMP commercial manufacturing as it relates to QA, Quality Systems, and the Supplier Qualifications Process. This key functional role will operate within a virtual function managing a QA team.
Our client a globally recognised brand is in growth mode locally here in Ireland and looking to recruit a QA Manager - External Manufacturing. The person will take on full responsibility for managing quality aspects at external sites for Biopharmaceuticals & Pharmaceuticals and to ensure that the operational business is in compliance with cGMP, the Quality Assurance Agreement, regulatory requirements and the corporate Pharma Quality handbook and is conducted according to the relevant SOPs.
Do you have experience of working as a Qualified Person on a Sterile / Biotech Drug Product site? Are you looking to broaden the scope of your role and move away from working just purely as a QP? If so then Clarity Recruitment have a role that you will be interested in.
Due to ongoing expansion plans this well known Pharmaceutical company is looking to hire an experienced and exceptional QA Manager for their open position on their state of the art manufacturing site in the South East of Ireland. The purpose of this job will be to manage and coordinate all Commercial Quality Assurance activities for the company.
You would be responsible for creating the best possible fit-for-purpose and competitive quotation based on user requirements at minimum cost, which are derived from Account Management transfer as well as from direct customer (an/or EPC; technical) interactions.
The positions will act as a Lead Engineer within an Oral Solid Dosage (OSD) site and reporting directly to the Sr. Director of Process Development. Responsibilities include management and oversight of multiple early and late stage development projects and support personnel.