Supervisor Biotech Production - Downstream (Shift)

Initial Therapeutics, Inc.; Ireland; On-site; EUR 80,000 - 110,000; Full time

Job summary

Regeneron in Raheen, Limerick, Ireland is seeking a Supervisor Biotech Production to join the Manufacturing team. You will lead and develop a team responsible for commercial-scale production of recombinant proteins in a cGMP environment.

The role requires strong leadership, hands-on supervision, and collaboration with Facilities, Process Development, QA and Quality Control to ensure quality, safety and regulatory compliance.

Qualifications

• BS/BA in Life Sciences or related field with 5+ years of cGMP manufacturing experience.
• Previous supervisory or leadership experience.

Responsibilities

• Supervise commercial scale manufacturing of recombinant proteins according to approved protocols and schedule.
• Lead a team responsible for the manufacture of bulk drug substance in a cGMP environment.
• Ensure safety, housekeeping, and regulatory compliance across operations.
• Review and edit batch records in line with cGMP standards.
• Coordinate scheduling, equipment maintenance, and batch tasks with master production schedule.
• Perform cGMP audits of production areas and manage personnel development.
• Interface with Facilities, Process Development, QA, and Quality Control.

Skills

Team leadership

cGMP manufacturing

Analytical skills

Communication skills

Education

BS/BA in Life Sciences

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
• Interfacing 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 a 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.

Equal Employment Opportunity Statement

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.