Principal Engineer - Process Validation - Leinster - beBeeEquipment

Job summaryThis job is an excellent opportunity to join a high-performing site where validation plays a strategic role in operational excellence. · Qualifications3+ years' experience in GMP pharmaceutical manufacturing · ...

Talent Crest is currently supporting a leading sterile pharmaceutical manufacturing site in Dublin with 2 positions within their Validation Department: Process Validation & Change Control. The roles sit at the core of GMP compliance, working closely with QA, Engineering, Manufact ...

Senior Validation Engineer - 2 Year Fixed Term Contract - Dublin (Hybrid) · Position Summary · Provide continuity for the validation program for assigned plant or functional area by writing, reviewing and approving validation documentation. Other duties may be assigned · Accounta ...

This role will require the candidate to provide process development support to new product introductions (NPI), technology transfer, lifecycle changes to syringe products, · provide subject matter expertise for product formulation, filling and characterisation to support producti ...

This role will provide process development support to new product introductions and lifecycle management changes. · -Support and lead new product introductions from concept to PPQ form a Process Development perspective · -Be accountable for the success of the product transfer pro ...

This role will require the candidate to provide process development support primarily to new product introductions (NPI) and lifecycle management (LCM) changes. · ...

Join an international team working to improve the future of healthcare at Grifols, a global healthcare company. · ...

We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. · Would you like to join an international team working to improve the future of healthcare? Do ...

The successful candidate will focus on the validation activities for a range of equipment solutions within a regulated Med Tech environment.You will both have responsibility for a number of activities and pieces of equipment while also supporting the wider Validation function and ...

We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. · Implement and execute tasks relating to Process, Facility and Equipment Development at PCI Pharma Services sites. · Ensure safe work practices are being followed at all time ...

We are seeking a Senior CQV Engineer to support our client's CAPEX projects in pharmaceutical manufacturing environment. The ideal candidate will have experience in validation, operations, engineering, and technical writing of GMP related documentation. · Prepare, review and appr ...

The validation department performs equipment utility facility cleaning and sterilization validation activities to ensure compliance with company procedures industry standards in support of Operations Quality Systems for Drug Product Manufacturing. · An exciting opportunity has op ...

We are currently recruiting for a CSV Engineer for our biopharmaceutical client in Dublin. This is an initial 12-month contract role. · ...

+An exciting contract opportunity for an experienced Senior Validation Engineer to support a large-scale Fill Finish pharmaceutical project. · + · +Develop and review User Requirement Specifications (URS) and Quality Risk Assessments for Equipment and Automated Systems (QRAES) · ...

We are looking for a Validation Engineer to join our team in Dublin, Ireland. The role involves supporting site validation activities and developing the site Validation Master Plan. · ...

+Join the Site Engineering Services department within the Small Molecule business unit of a leading pharmaceutical manufacturer as a CQV Engineer. · +Lead commissioning and qualification lifecycle ensuring all equipment meets cGMP standards. · Deliver high-quality technical docum ...

We are looking for a Senior Quality Assurance specialist in Dublin, Ireland. · ...

LSC have a great contract opportunity for a Cleaning Validation Engineer to join a Dublin based Biopharmaceutical company. · Performing all aspects of cleaning sampling required for cleaning validation for a new product. · ...

An External Manufacturing Lead is required for a biopharmaceutical company supporting commercial and clinical drug substance manufacturing. · ...

We are looking for a Validation Engineer to join a Pharmaceutical Company in Dublin to lead the commissioning, · validation and assembly documentation for a key project finalization. · ...

· Job Description · Job Opportunity: Quality Assurance Technician – Food Production · Location: Rathmooney, Dublin · About the Role: · Our client are seeking a dedicated and detail-oriented Quality Assurance Specialist to join their team within a leading food manufacturing compa ...