Ipsen in Ireland is represented by a dynamic state-of-the-art manufacturing facility dedicated to producing Active Pharmaceutical Ingredients (API's) for our core product portfolio.Due to business demands and capacity increase requirement, we are seeking enthusiastic and detail-focused individuals to join our Blanchardstown site asManufacturing Technologists, working 3 x 12 hr. shift premium– 38.5h in a three-week cycle (no nights).This 18-month fixed-term position is an excellent opportunity for anyone eager to build experience in pharmaceutical manufacturing. The role provides hands-on training, a 25% weekend shift allowance, and the chance to develop valuable industry experience. Successful applicants should be ready to start a training program beginning in January 2026. The program will run alongside the current downstream team - (4 Day working week Mon – Thurs & Tues – Fri) with the first working weekend commencing on March 27th, 2026.About The RoleThis weekend shift position plays a key role in maintaining continuous manufacturing operations and supporting overall site production throughput. As a member of the dedicated weekend team, you will ensure the seamless execution of GMP-compliant processes across multiple manufacturing platforms.Working within a regulatory environment, you will support both upstream and downstream processing activities and receive cross-functional training across Synthesis, Purification, and Cleanroom operations. This exposure offers the opportunity to develop a broad technical skillset and contribute directly to the manufacture of high-quality therapeutic products.Participate in structured training across both downstream and upstream operations, scheduled according to the current downstream work pattern (4 Day working week Mon – Thurs & Tues – Fri) This initiative aims to build cross-functional knowledge and enhance operational flexibility.Key ResponsibilitiesExecute daily production operations as directed by the Shift Lead and/or Manufacturing Manager, ensuring productivity, timeliness, and cost-efficiency while adhering to GMP and EHS standards.Oversee prompt and accurate completion of all batch related documentationPerforms daily production operations, as outlined by the shift lead and/or manufacturing manager, with a view to meeting the overall objectives of productivity, timeliness and cost while following GMP and EHS expectations.Carry out routine cleaning, sanitisation, and environmental control procedures.Support upstream and downstream activities, including synthesis, purification & lyophilisation.Complete batch record documentation and in-process checks in line with GMP standards, with a focus on submission to quality in a timely manner.Assist with equipment setup, operation, calibration, and troubleshooting.Participate in SOP revisions and continuous improvement initiatives.Adhere to all EHS and safety procedures, including risk assessments and deviation reporting.Rotate across functional areas (Synthesis, Purification, Cleanroom) as required to support production schedules and site priorities.Ensure high standards of housekeeping are maintained in the areaWork Pattern:3-week cycle on rotationWeek 1Friday: Rest daySaturday, Sunday, Monday: 07:00 – 19:00Week 2Friday: Rest daySaturday, Sunday, Monday: 07:00 – 19:00Week 3Friday: 07:00 – 14:30Saturday, Sunday, Monday : 07:00 – 19:00MinimumQualifications & ExperienceWorking knowledge of cGMP, EHS, and operational excellence principles.Ability to work both independently and collaboratively in a fast-paced, regulated environment.Demonstrated adaptability and teamwork across functional areas.Strong documentation accuracy and communication skills.PreferredDiploma in science related discipline, Ideally BSc. in science.2+ years' experience in a GMP-regulated environment.Familiarity with processing equipment, automation systems and peptide manufacturing.Experience with MES, SAP, and electronic batch record systems.Knowledge of Operational excellence and/or Lean Six Sigma.If you can point to an appropriate qualification and/or relevant experience, we would be delighted to engage with your application.