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Salary
$41k – $56k per year
Location
In office (Ireland)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 21, 2026. First seen by Alion on Oct 12, 2026. Takeda Pharmaceutical scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Takeda Pharmaceutical Company Limited is a global biopharmaceutical enterprise specializing in the research, development, and commercialization of targeted human therapeutics. The company focuses on core therapeutic areas including oncology, rare diseases, neuroscience, gastroenterology, plasma-derived therapies, and vaccines. Headquartered in Tokyo, Japan, it maintains extensive research, manufacturing, and commercial operations across more than 80 countries in Asia-Pacific, North America, Europe, and Latin America.

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

JOB PURPOSE:

Reporting to Plant Team Leader the Plant Technologist (Operator) has a very important role to play in Grange Castle’s commitment to quality and efficient manufacturing operations.

This is a shift-based role, requiring flexibility to work various shifts as part of our 24hr manufacturing operations

Responsibilities:

  • Perform duties as directed in whatever area of manufacturing operations they are currently assigned to. This would include (but not be limited to) processing, utilities, warehouse and inventory management as well as waste processing and management.
  • Carry out and monitor manufacturing operations (including all control system activities) as directed by, and in strict compliance with, the relevant manual or electronic Batch Manufacturing Instruction and Record (BMR) and Standard Operating Procedures (SOPs) or other Protocol.
  • Actively participate in problem identification, problem solving and change initiatives in cooperation with other teams and services. Continuous improvement with a cross functional focus is a core activity.
  • Actively support and contribute to the introduction of new processes and the execution of process validation by and under the direction of the relevant support personnel.
  • Ensure that the manufacturing and ancillary facilities are operated to optimum efficiency.
  • Ensure that the workplace and ancillary facilities are maintained in a clean and tidy state at all times and particularly during manufacturing activities.
  • Ensure that housekeeping duties are completed as assigned including the physical cleaning of process and ancillary facilities
  • Ensure that changeovers of both equipment and production areas are carried out in an efficient and effective manner.
  • Take and deliver samples to the laboratory; and if required complete any in-process testing assigned to them.
  • Carry out minor repairs/adjustments to plant and ancillary equipment where possible and as authorised.

Environmental, Health & Safety

  • Actively foster, in cooperation with other TILGC staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
  • Adhere fully to all safety policies, procedures and regulations.
  • Notify the Manufacturing Operations Manager/Designee (or other appropriate responsible person) in a timely and comprehensive manner of any:
  • Breach of HSE policy, procedure or regulation.
  • Potential hazard which could have a serious impact on safety or result in serious injury.
  • Ensure that Unplanned Event Forms are completed in a timely manner after an event.
  • Play an active role in the Site emergency response team and complete ERT training as required.

Quality Systems and GMP

  • Preparation of reports in relation to deviations and/or investigations, as required.
  • Proactively participate in auditing programmes as required but particularly in relation to contracted engineering and related services.
  • Notify the Manufacturing Operations Manager/Designee (or other appropriate responsible person) in a timely and comprehensive manner of any deviations from defined manufacturing processes or other established procedures. Any abnormal occurrences or observations should also be reported.
  • Generate documentation associated with their activities as required by cGMP, Health and Safety and Environmental regulations or management systems.
  • Ask, if in doubt, about any particular practice or unusual finding.

Training

  • Ensure that staff are well trained to safely and effectively carry out their roles. Develop training for relevant personnel with a particular focus on direct operational and technical support personnel.
  • Lead/actively participate in all training and assessment activities (internal and external) in relation to themselves, contractors or other employees.
  • Preparation and delivery of training materials.
  • Ensure timely completion of all SOP training and assessment tasks.
  • Ensure that all training and assessment is accurately and promptly recorded for themselves and other relevant personnel in accordance with TILGC procedures.
  • Maintain and improve their professional knowledge base. Keep up to date with all current trends and relevant legislation

General Responsibilities:

  • Participate fully in any cross functional training initiatives.
  • Drive and promote the corporate values of Takeda-ism within the workplace.
  • Drive and promote a culture of continuous improvement through all areas of the business
  • Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
  • Ensure timely completion of all SOP, reading, training and assessment.
  • Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.

Educational Requirements:

  • Leaving Certificate or equivalent,
  • Relevant 3rd level or technical qualification (is an advantage)

Relevant Experience:

  • 3 years experience in pharmaceutical industry, API experience preferable
  • Experience handling and working with hazardous chemicals
  • Distributed Control System (DCS) experience preferable.

Skills/Competencies:

  • Flexible, willing and positive attitude / mindset
  • Excellent verbal and written communication skills
  • Excellent planning, scheduling and prioritisation ability
  • Excellent documentation skills and attention to detail.
  • Excellent PC and systems skills.
  • Experience with Automation Production Systems e.g. MES

What you can look forward to with us:

  • Competitive Salary: Including performance-based bonuses.
  • Retirement Plan: Employer contributions to your retirement plan.
  • Comprehensive Insurance: Employer-funded private medical insurance with dependants’ cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
  • Electric Charging Points: Available at parking locations.
  • Employee Assistance Program: Support for personal and professional challenges.
  • Wellbeing and Engagement: Dedicated teams to support your wellbeing.
  • Family-Friendly Policies: Supportive policies for a balanced work-life.
  • Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
  • Development Opportunities: Coaching, mentoring, educational programs, and formal training.
  • Subsidized Canteen: Enjoy meals at a reduced cost.
  • Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering our people to shine:

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.

If you are interested in this opportunity, we look forward to receiving your application via our online tool!

Locations

Grange Castle, Ireland

Base Salary Range:

€36,100.00 - €49,610.00

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.

For information about our benefits, please click here.

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
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