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Manufacturing Technologist
Job details
Job type
Shift and schedule
Full job description
Ready to make an impact in a fast-paced manufacturing environment?
Due to business demands and capacity increase requirement, we are seeking enthusiastic and detail-focused individuals to join our Blanchardstown manufacturing facility as Manufacturing Technologists, working 3 x 12 hr. shift premium– 38.5h in a three-week cycle (weekend 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.
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. 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: Three -week cycle on rotation
Week 1
Friday - Sunday: 19:00 – 07:00
Monday: Rest Day
Week 2
Friday - Sunday: 19:00 – 07:00
Monday: Rest Day
Week 3
Friday - Sunday: 19:00 – 07:00
Monday: 19:00 – 02:30
Qualifications & Experience
Minimum:
- 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 have the right qualification and/or relevant experience, and you’re ready to grow your skills in a GMP manufacturing environment, we’d love to hear from you.