Are you an experienced QP with strong Quality Systems Management experience in either Steriles or Biologics? If so, this pharmaceutical job will be of interest to you! 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.
Are you a Quality Manager or a QP with strong Quality Systems Management experience in either Steriles, Biologics and/or GDP sites? Looking for the next step in your career? If so then Clarity Recruitment has the perfect pharmaceutical job for you!
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.
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.
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.
A top 20 global pharmaceutical company with an ever-growing drug portfolio is looking to recruit a new Senior Project Manager for their Global Manufacturing department.
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.
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.
This Qualified Person will act as a key member of the Quality Assurance team associated with the production of our client’s Biologics product.
This QC Lab Manager will have responsibility for all chemistry and microbiological testing activities at this manufacturing campus in Dublin while reporting directly to the site quality head
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?
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.
The successful candidate will be responsible for overseeing all quality operations during the development process of this state of the art drug substance Manufacturing, located in Dublin.
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.
An exciting new opportunity has arisen for a Lead Account Manager working with a global leader in industrial automation solutions covering the Island of Ireland. This company operates across a wide portfolio of industries within this region such as: Chemicals, Food and Beverage, Utilities, Supply Chain and Pharmaceuticals.
This is a brand new role for this global top 20 Pharmaceutical company, where the successful candidate will be responsible for the Global Master Planning of products produced here in Ireland.
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.
An exciting new opportunity has arisen for a QC Microbiology Manager (12 month contract - maternity cover) to work with a world leading food manufacturer within their Quality department. The position would be based in one of the company’s sites in South - East Ireland.
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 tremendous developments on this manufacturing site in recent years, our client, a major global player in their particular industry globally are looking to recruit a Process Manager with an engineering focus to oversee optimisation of all plant processes with a major focus on Quality/Hygiene and end of process product standards.
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.
An exciting opportunity has arisen within the Marketing department for a Market Insights Manager for the Global Regions for a globally well known FMCG organisation. This senior level role will report to the Group Head of Marketing and will have responsibility for providing intelligence and insight on targeted international markets to drive commercial and innovation strategy primarily.
You would be a key quality specialist within the department responsible for supporting the Senior Directors and VPs. The main focus areas for the role will be on technical deliver of projects, including acting as a QP and rolling out compliance audits.
As part of this exciting position your key responsibility for the site will be to ensure the successful management of the QA / Technical function for the site ensuring they maintaining their BRC accreditation as well as make sure that the Highest of Food Safety and hygiene standards are upheld and achieved as common practice.