Manufacturing Technologist

Title:

Company:

About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.

Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram.

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.

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.