Production Technologist

IRL - 1500 Takeda Ireland Limited; Ireland; On-site; EUR 30,000 - 41,000; Full time

Job summary

Takeda Ireland Limited in Bray, Ireland, is seeking a production-focused employee to manufacture and package products in line with GMP and BMR procedures. You will ensure strict cGMP adherence, complete checks, and maintain a high-quality attitude in a fast-paced manufacturing environment.

The role requires 1 year in a pharmaceutical setting, basic PC literacy, and a willingness to learn new tools. A Leaving Certificate or equivalent is required, with a fixed-term, full-time work arrangement in

Qualifications

• Minimum 1 year previous experience in a Pharmaceutical environment.
• A third level science qualification (Cert./Diploma) would be an advantage.
• Leaving Certificate qualification or equivalent.

Responsibilities

• Manufacture/Packaging of product according to the production schedule and GMP.
• Maintain adequate stock levels of production consumables.
• Work with engineering to resolve downtime and maximise productivity.
• Carry out visual inspection of finished product in packaging/processing areas.
• Adhere to company policies and participate in cross-functional training.
• Promote safety culture and complete accident/near-miss reports.

Skills

Basic PC literacy

Interpersonal / communications

Willingness to learn / apply new tools

Education

Leaving Certificate

Job description

Job Description

JOB PURPOSE

This brief demands a commitment to the Production effort, i.e., the production of finished pharmaceutical products of the required quality.

RESPONSIBILITIES

Quality /Safety/5S: Compliance with TIL quality standards and cGMP pertaining to Production. Manufacture of product in strict compliance with procedures and batch manufacturing records (BMR’s), incorporating cGMP and safety procedures. Accurate and timely completion of all relevant checks as per Electronic Batch Records and ancillary paper documents. Maintain an awareness of the focus areas for bGMP to ensure the correct attitudes and behaviors towards GMP are maintained within your work centre. Generation of relevant Standard Operating Procedures and Manufacturing Batch Records as required Maintain your work place to a high degree of GMP adherence with particular attention to the company 5S program. Ensure all relevant equipment and in-process test equipment is in calibration. Strict compliance with all safety procedures including the reporting of all accidents / near misses. Full cooperation with all onsite safety initiatives. Performance & Continuous Improvement Maintain a flexible approach to the daily tasks assigned to you within your work centre. Achievement of the Key Performance Indicator targets. Strong willingness to learn / apply new tools / techniques. Practical application of Lean Tools; SMED, RCA, Kaizen, FMEA & 5S. Actively participate in the achievement of the relevant KPI’s for your work centre as outlined in the Continuous Improvement Program Employee participation in cross functional training Active participation in performance dialogues. Process: Manufacture/Packaging of product according to the production schedule and GMP. Ensure that adequate stock levels of production consumables for selected work-centre(s) are maintained at all times Work closely with engineering to ensure the timely resolution of downtime issues so as to maximize the productivity of your assigned work centre. Active participation in addressing processing/packaging issues in conjunction with other departments as required. Carry out visual inspection of finished product in the packaging/processing areas as required. General: Strict adherence to all company policies with particular focus on all Leave, Employment & Employee Benefits policies GENERAL RESPONSIBILITIES: Participate fully in any cross functional training initiatives. Drive and promote the corporate values of Takeda-ism within the workplace. 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 that Accident Reports / Near Miss Forms are completed in a timely manner after an event. Ensure timely completion of all SOP, reading, training and assessment. Other duties as required and directed by the Manager, Production or other Officer appointed by the Board of Directors.

EDUCATIONAL REQUIREMENTS

Leaving Certificate qualification or equivalent

RELEVANT EXPERIENCE

Minimum of 1 year previous experience in a Pharmaceutical Environment preferable. A third level science qualification (Cert./Diploma) would be an advantage.

SKILLS/COMPETENCIES

Basic PC literacy essential Good interpersonal / communications skills Willingness to learn / apply new tools / techniques essential

Locations

Bray, Ireland

Base Salary Range

€29,800.00 - €41,030.00 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.

Worker Type

Employee Worker Sub-Type Fixed Term (Fixed Term) 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 an equal opportunity employer.

If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability