Supervisor Biotech Production - Downstream (Shift)

Regeneron; Limerick; On-site; EUR 54,200 - 88,400; Full time

Job summary

Regeneron is seeking a Supervisor Biotech Production to join the Manufacturing team in Raheen, Limerick. The role involves supervising commercial-scale manufacturing of recombinant proteins, ensuring cGMP compliance and timely execution of the master production schedule.

The ideal candidate will have a BS/BA in Life Sciences, 5+ years of cGMP manufacturing experience, and prior supervisory experience. The position requires day/night/weekend shifts and a strong focus on safety and team leadership.

Qualifications

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

Responsibilities

• Supervise commercial-scale manufacturing of recombinant proteins per approved protocols and schedules
• Oversee batch records in a cGMP regulatory environment and ensure readiness of production batch records
• Ensure equipment readiness, calibration, and maintenance; coordinate maintenance activities
• Conduct cGMP audits of production areas and enforce safety and housekeeping standards
• Manage personnel including timesheets, vacations, training, development and performance reviews

Skills

Troubleshooting

Analytical skills

Team leadership

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 edits 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 coordinates regular equipment maintenance and calibrations; troubleshoots 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.

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.

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