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Associate Biotech Production Specialist

Regeneron

Associate Biotech Production Specialist

full-timePosted: Aug 4, 2026Updated: Sep 1, 2026Limerick

Job Description

Build our future together:Within this role you will be working as part of the Manufacturing Team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors. Where: Location: Raheen, LimerickShift: 24/7What you’ll do:Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and SupervisorsMonitoring production processesParticipating in equipment start-up, commissioning, and validation activitiesAssisting with troubleshooting in case of equipment failurePerforming manufacturing level maintenance on equipmentAdhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasksPerforming equipment cleaning, preparation and execution as well as completing associated documentationPerforming various tests and in-process samplingReviewing, editing and revising completed batch records, logbooks, and SOPs in accordance with cGMP standardsMaintaining housekeeping in designated area and adhering to the clean standards of the facilityThe environment and physical rhythms of this role:You possess excellent verbal and written communication skillsYou enjoy problem solvingYou demonstrate a can-do attitudeYou are proficient in Microsoft Word, Excel, PowerPoint, and OutlookYou demonstrate an ability to work within a successful teamYou can adapt to a changing environment and have the ability to adhere to a scheduleLet’s find out if we’re a fit:To be considered for this opportunity you should have a BS/BA in Life Sciences or a related field. Relevant experience may be substituted in lieu of the educational requirementOur site operates on a 24/7 basis, and we offer a number of different shift working patterns that could fit with your lifestyleWhat is on offer? You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:Competitive SalaryShift PremiumsAnnual BonusStock SchemesEmployer Pension Contributions Education AssistanceGenerous Annual & Flexible Leave Programs Competitive Private Medical, Dental & Vision PlansCareer & Personal DevelopmentWellness Programs - Onsite Gyms & Fitness Classes Concierge Services – Onsite Beauty Therapist / BarberCommunity VolunteeringEmployee Interest Groups / Employee Teams & ClubsEmployee & Family EventsThrive today. Grow tomorrow.#LI-Onsite #JOBSIEST #REGNIELSM #IRELIMDoes this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.For jobs in Canada: this posting is for an existing position.Salary Range (hourly)€16.42 - €25.59

Locations

  • Limerick

Responsibilities

  • Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors
  • Monitoring production processes
  • Participating in equipment start-up, commissioning, and validation activities
  • Assisting with troubleshooting in case of equipment failure
  • Performing manufacturing level maintenance on equipment
  • Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks
  • Performing equipment cleaning, preparation and execution as well as completing associated documentation
  • Performing various tests and in-process sampling
  • Reviewing, editing and revising completed batch records, logbooks, and SOPs in accordance with cGMP standards
  • Maintaining housekeeping in designated area and adhering to the clean standards of the facility
  • Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors
  • Monitoring production processes
  • Participating in equipment start-up, commissioning, and validation activities
  • Assisting with troubleshooting in case of equipment failure
  • Performing manufacturing level maintenance on equipment
  • Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks
  • Performing equipment cleaning, preparation and execution as well as completing associated documentation
  • Performing various tests and in-process sampling
  • Reviewing, editing and revising completed batch records, logbooks, and SOPs in accordance with cGMP standards
  • Maintaining housekeeping in designated area and adhering to the clean standards of the facility

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