Plant Technologist
IRL - 1500 Takeda Ireland Limited
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Job summary
Takeda Ireland Limited, Grange Castle, Ireland, is seeking a Plant Technologist (Operator) to support 24hr manufacturing operations. The role is shift-based, requiring flexibility to work various shifts as part of our continuous production.
You will operate across processing, utilities, warehouse and inventory tasks, following BMR/SOPs, and contribute to problem solving, continuous improvement and process validation.
Qualifications
- Leaving Certificate or equivalent; 3rd level qualification is an advantage.
- 3 years experience in pharmaceutical industry, API experience preferable.
- Experience handling hazardous chemicals.
- Distributed Control System (DCS) experience preferable.
Responsibilities
- Perform duties across manufacturing areas including processing, utilities, warehouse and inventory.
- Operate and monitor manufacturing processes per BMR/SOPs or other protocols.
- Participate in problem solving and continuous improvement with cross-functional teams.
- Support introduction of new processes and process validation.
- Ensure facilities run at optimum efficiency and keep areas clean.
- Take samples to laboratory and perform in-process testing as required.
Skills
Education
Tools
Job description
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.
- 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.
- 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.
- Notify the Manufacturing Operations Manager/Designee (or other appropriate responsible person) in a timely and comprehensive manner of any 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.
- 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.
- 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.
- 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.
Leaving Certificate or equivalent, Relevant 3rd level or technical qualification (is an advantage)
- 3 years experience in pharmaceutical industry, API experience preferable
- Experience handling and working with hazardous chemicals
- Distributed Control System (DCS) experience preferable.
- 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
- 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.
Grange Castle, Ireland
€36,100.00 - €49,610.00
Employee Worker Sub-Type Regular Time Type Full time
Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.
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.
Takeda is an equal opportunity employer.
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.
For applicants of U.S and Puerto Rico positions: Learn about our commitment to Equal Employment Opportunity (EEO).
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