Supervisor Biotech Production - Downstream (Shift)

Regeneron Pharmaceuticals, Inc; Munster; On-site; EUR 54,200 - 88,400; Full time

Benefits offered by this job

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Supervisor Biotech Production to join our Manufacturing team in Raheen, Limerick. The role offers an opportunity to lead a team responsible for commercial scale production of recombinant proteins in a cGMP environment.

You will supervise batch records, coordinate maintenance, schedule tasks, and mentor staff while upholding safety and quality standards. The position requires a BS/BA in Life Sciences and 5+ years of cGMP manufacturing experience with

Qualifications

• Requires BS/BA in Life Sciences or related field with 5+ years of relevant cGMP manufacturing experience.
• Experience in supervision/leadership roles.
• Strong analytical and communication skills.

Responsibilities

• Supervising commercial scale manufacturing of recombinant proteins in a cGMP environment.
• Leading a team responsible for bulk drug substance production and ensuring schedules are met.
• Reviewing and editing batch records in line with cGMP standards.
• Ensuring availability of production batch records for upcoming lots and coordinating scheduling.
• Overseeing equipment readiness, maintenance, and calibration; troubleshooting as needed.
• Conducting cGMP audits of production areas and enforcing safety standards.
• Managing people, including time sheets, vacations, training, and performance evaluations.
• Interfacing with Facilities, Process Development, Regulatory, QA and QC.

Skills

Team leadership

cGMP manufacturing

Quality coordination

Batch records review

Problem solving

Communication skills

Education

BS/BA in Life Sciences or related field

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Supervisor Biotech Production to join our Manufacturing team.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Location: Raheen, Limerick
• Other information: You will be required to work shift (days, nights, weekends)

What you’ll do:

• Supervising commercial scale manufacturing of recombinant proteins according to approved protocols, regulation, and schedule
• Supervising a team responsible for the manufacture of bulk drug substance in a cGMP regulatory environment
• Ensuring that the highest safety and housekeeping standards are maintained
• Supervising all aspects of respective areas of operations
• Reviewing and editing batch records in accordance with cGMP standards
• Ensuring availability of production batch records for upcoming lots
• Scheduling duties and batch tasks based on master production schedule
• Ensuring equipment readiness and coordinating regular equipment maintenance and calibrations; troubleshooting equipment
• Performing cGMP audits of production area
• Performing people management duties including time sheet submissions, scheduling of vacations, personnel development, disciplinary actions, hiring, terminations, and performance evaluations
• Scheduling individual and ongoing training
• Interfaces with other departments, such as Facilities, Process Development, Process Analytical Sciences, Regulatory, Quality Assurance and Quality Control

The environment and physical rhythms of this role:

• You possess logical troubleshooting and problem‑solving skills
• You have excellent analytical, written and oral communication skills
• You demonstrate an ability to work with and supervise a successful team

Let’s find out if we’re a fit:

• Requires BS/BA in Life Sciences or related field with 5+ years of relevant cGMP manufacturing experience and some previous supervisory/leadership experience. Will substitute relevant experience in lieu of educational requirement.

Thrive today. Grow tomorrow.

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.

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/.

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 (annually)

€54,200.00 - €88,400.00