Pharmaceutical Compliance Specialist

About This RoleThis is an exciting opportunity to join a leading global pharmaceutical company as a Complaints Processing Analyst.You will play a crucial role in ensuring customer complaints are handled efficiently and in compliance with global regulations.As a Complaints Processing Analyst, you will oversee investigations, identify root causes, and track...

About Sigmar RecruitmentWe are a leading recruitment agency in the pharmaceutical industry, specializing in contract and permanent roles.Our expertise lies in matching top talent with organizations that require their skills. We understand the importance of finding the right candidate for the job, which is why we take the time to get to know our clients'...

Team Horizon is seeking an experienced Validation Engineer for the role of Pharmaceutical Technology Specialist for our Client who are based in Co. Mayo. The successful candidate will be part of the Validation Department who are responsible for the qualification / validation of all CGMP equipment, systems and processes. The role of the Pharmaceutical...

SRM Specialist - Pharmaceuticals - 12-Month Contract  Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for SRM Specialist to join their state of the art pharmaceutical facility. Located in the historic province of Connacht neighbouring the pond that is the Atlantic Ocean, breeds a mix of Irish culture and...

Engineering Project Specialist Team Horizon is seeking a Engineering Project Specialist for a leading pharmaceutical company in Mayo. The successful candidate will be responsible for safely coordinating and leading projects associated Facility, Utility and Equipment Projects. Key areas of responsibility include but (not limited to) on time and budget...

Your new company Here at HAYS Life Sciences we have a fantastic permanent opportunity with our client, a well established global biotechnology company with customers in sectors such as pharmaceutical, biotechnology, agrochemical, governmental, and academia. They would be large-scale organization who specialise in research, drug discovery and development,...

Company Description Join Our Team as a Regulatory Affairs Specialist (1-Year Fixed Term Contract) Are you ready to make a significant impact in the medical device industry? Were seeking a dedicated Regulatory Affairs Specialist to join us on a 1-year fixed term contract. This role will be based in Ballina, Co. Tipperary, with flexibility for onsite...

About Your New Job Join a leading global pharmaceutical company with a strong reputation for innovation and excellence.This is your opportunity to work on cutting-edge products in a collaborative and dynamic environment.This is a 12-month contract based in As a Complaints Processing Analyst, you will play a crucial role in ensuring customer complaints are...

Are you passionate about making a difference in the lives of individuals with autism? Do you have a strong background in managing residential services and a commitment to delivering high-quality care?We are seeking an Autism Care Specialist to join our team as a Service Manager - Mayo. In this critical role, you will be responsible for ensuring the highest...

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will...

About Your New JobThis is an excellent opportunity to join a leading global pharmaceutical company as a Quality Complaints Analyst.As a Quality Complaints Analyst, you will be responsible for ensuring all complaint records meet global regulatory requirements.You will investigate and document product complaints, including root cause analysis and CAPA...

Job Summary:We are seeking a highly skilled Quality Complaints Analyst to join our team. As a Complaints Processing Analyst, you will play a crucial role in ensuring customer complaints are handled efficiently and in compliance with global regulations.Your responsibilities will include overseeing investigations, identifying root causes, and tracking...

GerTek offers a dynamic work environment where you will contribute to pioneering solutions in the biopharmaceutical industry.As a Senior Project Engineer, you will lead cross-functional project teams to deliver processing equipment on time and within budget.Your responsibilities will include writing User Requirement Specifications, vendor selection, and...

RequirementsTo be successful in this role, you will need:A Third-Level qualification in a suitable manufacturing, engineering, or business course, and/or suitable experience.A minimum of 7 years authoring experience, having led or been a technical lead on multiple implementation projects.Proficiency with MES application and configuration rules and...

About the Role:We are seeking an experienced Quality Complaints Analyst to join our team. As a Complaints Processing Analyst, you will be responsible for ensuring customer complaints are handled efficiently and in compliance with global regulations.Your responsibilities will include overseeing investigations, identifying root causes, and tracking...

Gertek Project Management is dedicated to providing project management, talent solutions, and commissioning qualification and validation services to life science and technology companies.We partner with these companies to deliver their most strategic and important projects.The Project Development Specialist plays a critical role in ensuring that projects...

Mechanical Site Supervisor with 8+ years experience required to join a large Mechanical and Electrical Contractor to work on large pharmaceutical project in Westport, Mayo.The successful Mechanical Site Supervisor will have a proven track record of delivering projects from inception to final handover and will report to the Contracts Manager.The client will...

Team Horizon is seeking a Manufacturing Shift Manager for our client based in Mayo. In this role you will lead and facilitate the safe operations of the 24/7 Biologics manufacturing team in a bio-pharmaceutical processing facility in line with all safety, regulatory and operational requirements. This is a shift based role, you will be required to work...

An exciting opportunity for a Biopharma Manufacturing Lead to join a Biologics Leader in the West of Ireland . The Biopharma Manufacturing Lead will be responsible for organising and planning all operations , ensuring Manufacturing Technicians follow schedules set by Supply Chain and other stakeholders. Ensure all activities comply with EHS and...

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will...