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 as
Manufacturing 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 Role
This 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 Responsibilities
* Execute 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 documentation
* Performs 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 area
Work Pattern:
3-week cycle on rotation
Week 1
Friday: Rest day
Saturday, Sunday, Monday: 07:00 – 19:00
Week 2
Friday: Rest day
Saturday, Sunday, Monday: 07:00 – 19:00
Week 3
Friday: 07:00 – 14:30
Saturday, Sunday, Monday : 07:00 – 19:00
Minimum
Qualifications & Experience
* Working 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.
Preferred
* Diploma 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.