Pharmaceutical Documentation Manager

At Cpl Healthcare, we are seeking a highly skilled Senior Pharmaceutical Documentation Specialist to join our team. In this role, you will be responsible for maintaining the document management system DCA (Document Control and Archiving) and liaising with cross-functional departments on documentation requests and issues.Key Responsibilities:Maintain the...

Are you a motivated and experienced professional looking for a new challenge? Do you have a passion for improving patient lives? We are seeking a highly skilled Regulatory Compliance Specialist to join our team at West Pharmaceutical Services, Inc.The successful candidate will have a strong background in regulatory compliance, with experience in implementing...

Job DescriptionThe Regulatory Operations Associate will report directly to the Regulatory Affairs Manager and be responsible for ensuring the accurate and timely submission of electronic regulatory documents for existing licensed products for life cycle maintenance and new submissions.This includes performing necessary tasks such as photocopying, scanning,...

Job DescriptionThe Qualified Person will be responsible for ensuring the quality of medicinal products manufactured at West, including batch certification and release. This role requires a strong understanding of EU GMP regulations and experience in setting up and maintaining a QMS.Key Responsibilities:Ensure compliance with EU GMP regulations and...

We are currently recruiting for a Pharmaceutical Operations Manager position with an award-winning Pharmaceutical organization based in Dublin. This is an excellent opportunity for a professional looking to work with a leading multinational company that excels in its field.Job DescriptionThis role will involve oversight of validation activities at External...

We are seeking a highly motivated Quality Assurance Systems Administrator to join our team at the Swords Campus. As a key member of the Quality Systems team, you will be responsible for maintaining the document management system DCA and providing administrative support to the team.Key ResponsibilitiesThe successful candidate will be responsible...

Lead Document Controller - Pharmaceuticals - County Roscommon, Ireland  Our client, a global (bio)pharmaceutical manufacturing organisation, is recruiting for a Lead Document Controller to join them on their new expansion project. Based in a charming Nordic location, this is on a contractual basis, and will involve significantly growing the sites...

Cpl Healthcare has partnered with Thornshaw Scientific to deliver a new opportunity for a highly skilled EU Pharmaceutical Regulatory Manager. This exciting role involves managing EU marketing authorisation dossiers and submissions, preparing and filing EU submissions, and communicating effectively with European Regulatory Authorities.The successful...

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...

Cpl Healthcare is collaborating with a global pharmaceutical company to recruit a Regulatory Affairs Officer to join their Dublin team.**Job Summary:**This role will focus on managing EU marketing authorisation dossiers and submissions.You will prepare and file EU submissions, write local modules, and compile regulatory documentation.Effective communication...

About the RoleThe Senior Technical Documenter will be responsible for managing the creation, review, and approval of technical documents in support of engineering projects. This role requires strong attention to detail, excellent communication skills, and the ability to work effectively in a fast-paced environment.Main Responsibilities:Manage the technical...

Job DescriptionThis role is for a QA Systems Administrator who will be responsible for maintaining the document management system DCA (Document Control and Archiving) and liaising with cross-functional departments on documentation requests and issues.The successful candidate will be based at our Swords Campus and will be part of the Quality Systems team. You...

Job SummaryThe Engineering Documentation Specialist will be responsible for creating, maintaining, and controlling engineering documents and records in accordance with company policies and industry standards. This role requires a high level of accuracy, attention to detail, and organizational skills.Main Duties:Prepare and revise engineering documents,...

About UsSK Pharmteco, a company we are proud to partner with, is a global Contract Development and Manufacturing organisation (CDMO) with state-of-the-art facilities in Korea, US, France and Ireland.Our mission is to'make what matters for a healthy, happier world', from grams to tonnes. With a talented workforce, exceptional technical capabilities, and...

Required Skills and Qualifications:Proven experience in a lead turnover engineer role or similar, within the pharmaceutical or life sciences industry.Strong knowledge of turnover procedures, documentation, and regulatory compliance.The successful candidate will have excellent communication and leadership skills, as well as the ability to manage multiple...

About the RoleAs an Instrumentation Engineer, you will play a key part in our client's Centre of Excellence for veterinary vaccine development. With over [number of employees] colleagues, we are looking to add an experienced professional to our team.The successful candidate will be responsible for overseeing external vendors performing maintenance and...

West Pharmaceutical Services, Inc is a dedicated team that is connected by a purpose to improve patient lives. Our story began with Herman O. West who solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions...

Hrm Recruitment Limited is pleased to partner with a leading pharmaceutical and biotech organisation in the recruitment of a Qa/Ra Manager. The successful candidate will join a growing team based out of Dublin, Ireland, and will play a key role in contributing to the development and marketing of life-changing products.As a Qa/Ra Manager, you will be...

We are seeking a highly motivated and experienced Pharmaceutical Quality Associate to join our team at Lifescience recruitment. As a Pharmaceutical Quality Associate, you will play a key role in ensuring that all manufacturing processes meet the highest standards of quality and compliance.Your primary responsibility will be to review and approve GMP...

**Mission Critical Power Solutions**Cel Critical Power is a world-leading provider of mission-critical power distribution solutions. Our expertise spans high-performance switchgear, PODs (Power Distribution Units), and control systems for data centers and pharmaceutical facilities worldwide.We are seeking a talented Technical Writer to create high-quality...