GMP Manufacturing Expert

We are seeking a skilled GMP Manufacturing Operations Expert to join our team. In this role, you will be responsible for supporting cleaning validation, including recovery/cleanability studies, and ensuring compliance with regulatory requirements and cGMP guidelines.The ideal candidate will have considerable experience in a comparable role, with experience...

PSC Biotech Corporation is seeking an experienced GMP Compliance Expert to join our Engineering Department. In this role, you will be responsible for ensuring that our company's products meet the highest quality and safety standards.About UsPSC Biotech Corporation is a leading Biotech Consultancy firm with operations globally. We provide cloud-based software...

LSC offers a unique contract opportunity for a Validation Engineer to join a pioneering Biopharmaceutical company in Ireland.This state-of-the-art manufacturing facility produces a range of products across various therapeutic areas, including oncology, autoimmunity, pneumonia, and infectious disease.Design, develop, review, approve, and execute...

Key ResponsibilitiesAs a GMP Compliance Professional at PSC Biotech Ltd, you will be responsible for ensuring compliance with global policies, procedures and guidelines, as well as regulatory requirements. You will design/author/review/approve/executes qualification/validation documentation and cycle development studies, and engage with production,...

PE Global is seeking a highly skilled Validation Engineer to join our team in a GMP manufacturing environment.About the RoleThe successful candidate will be responsible for supporting Cleaning Validation, including Recovery/Cleanability studies, and will work closely with production, maintenance, and quality teams to ensure seamless execution of Cycle...

We are recruiting an experienced Sterile Manufacturing Expert to lead our client's site microbiology department. As the Associate Director, you will play a vital role in delivering life-changing medicines to patients globally.Your primary responsibility will be to ensure the highest standards of microbiological quality in a world-class biologics environment....

About the RoleWe are seeking a highly skilled Manufacturing Process Specialist to join our team. The successful candidate will have a Bachelor's Degree or higher in a Science, Engineering, or other Technical discipline.The ideal candidate will have a minimum of 3 years' experience in manufacturing, preferably in a GMP Setting. They will demonstrate evidence...

Opportunity OverviewWe are seeking a highly skilled Compliance Engineer to join our client's team in Carlow, Ireland.This contract opportunity is ideal for a quality professional with 3 years of experience in the pharmaceutical or biotechnology industry looking to take on new challenges and responsibilities.Key Responsibilities:Deliver quality oversight and...

About PSC Biotech LtdWe are a leading biotechnology consultancy firm with global operations. Our mission is to provide high-quality solutions to our clients in the pharmaceutical and biotechnology industries.As a Process Validation Expert at PSC Biotech Ltd, you will be responsible for designing, authoring, reviewing, approving and executing...

About the Job:The GMP Engineering Lead is responsible for supporting the Engineering Department in a GMP environment. This role ensures that objectives are effectively achieved, consistent with client requirements to ensure compliance, safety, and reliable supply to customers.Main Responsibilities:Lead deviations, out of tolerance conditions, and unexpected...

Job DescriptionWe are looking for a Sterile Manufacturing Specialist to join our team. As a Sterile Manufacturing Specialist, you will be responsible for leading process engineering and validation activities to support the technical transfers, as well as managing multiple Technical Engineering projects needed to support the business.The ideal candidate will...

Job Description">Key Responsibilities:">Design, author, review, and execute qualification/validation documentation and process development studies in line with the standard approval process.">Provide technical input into quality notifications by authoring/reviewing/approving investigations.">Serve as a technical engineering representative for internal...

About PSC Biotech CorporationWe provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.PSC Biotech Corporation is a leading Biotech Consultancy firm founded in 1996, headquartered in California, USA, with Global operations in...

About the JobWe are recruiting for a highly skilled and experienced Sterile Manufacturing Engineer to join our team at Recruitment by Aphex Group. This is an exciting opportunity for a technical professional who is passionate about leading the development of sterile manufacturing facilities.Key ResponsibilitiesTechnical Leadership: Lead activities to deliver...

PE Global is seeking a seasoned expert to join our team as a Validation Engineer in a GMP manufacturing environment.About the RoleThe successful candidate will be responsible for supporting Cleaning Validation, including Recovery/Cleanability studies, and will work closely with production, maintenance, and quality teams to ensure seamless execution of Cycle...

About the RoleWe are seeking a highly skilled and experienced Manufacturing Technical Lead to join our team at Recruitment by Aphex Group. This is an exciting opportunity for a technical professional who is passionate about leading the development of drug product facilities.Key ResponsibilitiesTechnical Leadership: Lead activities to deliver on Tech Transfer...

Role Summary: We are recruiting for an Associate Director, Site Microbiologist to lead our client's site microbiology function in Ireland. This is a unique opportunity to join a cutting-edge biologics site and contribute to the development of life-saving treatments.As a Subject Matter Expert (SME) on microbiological matters, you will provide guidance across...

Job DescriptionThis role serves as a technical support specialist for new product introduction and commercial manufacturing. The successful candidate will have prior related work experience, preferably in a GMP Setting.Key responsibilities include designing and executing qualification/validation documentation, process development studies, and change...

We are seeking a highly skilled Validation Engineer to join a leading Biopharmaceutical company in Ireland.This innovative manufacturing facility produces a wide range of products across various therapeutic areas, including oncology, autoimmunity, pneumonia, and infectious disease.Develop, implement, review, approve, and execute qualification/validation...

About the OpportunityThis is a fantastic opportunity to join a leading healthcare company and contribute to the advancement of manufacturing excellence and R&D across our Irish sites and global company network.About the JobWe are seeking a highly skilled Validation Process Expert to join our team. The successful candidate will have a strong background in...