Spvr Quality Control

Regeneron Pharmaceuticals; Rensselaer (IN); Presencial; USD 79.000 - 129.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual bonuses

Health benefits

401(k) company match

Paid time off

Family support benefits

Descripción de la vacante

Regeneron Pharmaceuticals, located in United States, seeks a QC Supervisor to join the QC Drug Product Packaging team onsite in Rensselaer, NY. You will oversee lab activities supporting testing and release of Drug Product Packaging and Medical Device Components.

The role involves supervising QC staff, ensuring cGMP compliance, writing SOPs, and contributing to audits and training. This is a hands-on leadership position within a fast-growing, science-driven organization.

Formación

• Requires BS/BA in Life Sciences or related field, MS preferred, with 5+ years of progressive experience.
• Supervisory/leadership experience required.
• Pharmaceutical/biotechnology industry experience preferred.

Responsabilidades

• Supervises QC staff, distributes workload, and monitors progress.
• Reviews study protocols and reports.
• Attends meetings to stay informed of development and manufacturing priorities.
• Ensures compliance with cGMP regulations and SOPs.
• Organizes lab investigations and troubleshooting as necessary.
• Writes and revises SOPs, methods, protocols, and reports.
• Supports internal and regulatory audits.
• Ensures proper training and safety standards.

Conocimientos

Quality control

People management

GMP compliance

SOP writing

Educación

BS/BA Life Sciences

MS Life Sciences

Descripción del empleo

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a QC Supervisor to join our QC Drug Product Packaging team, supporting our Quality Control organization in an on-site work model. In this role, you will provide front line support for laboratory activities to support the testing and release of Drug Product Packaging and Medical Device Components.

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

When & where:

• Location: Rensselaer, New York, United States
• Working model: Sunday – Thursday, 8AM – 4:30PM

Discover your role:

• Supervises QC staff, distributes workload, and monitors progress.
• Reviews study protocols and reports.
• Attends meetings to keep informed of development and manufacturing priorities and activities.
• Ensures compliance with applicable cGMP regulations and SOPs.
• Organizes lab investigation and assay trouble shooting as necessary.
• Performs personnel management functions including time sheet submissions, scheduling of vacations, personnel development, and performance evaluations.
• Writes and revises SOPs, methods, protocols, and reports.
• Oversees daily operation of activities in area.
• Supports internal and regulatory audits.
• Ensures personnel receive proper and prompt training.
• Ensures that safety standards are maintained.

This role might be for you if:

• You excel in a quality-driven organization
• You manage multiple assignments and shifting priorities with strong organizational and project-management skills
• You bring exceptional attention to detail and strong prioritization skills
• You communicate clearly and effectively with direct reports, peers, and leadership
• You have prior management or supervisory experience
• You adapt quickly to shifting priorities while juggling multiple tasks and deadlines
• You have experience working in a GMP environment

This role requires:

• Requires BS/BA in Life Sciences or related field, MS preferred, with 5+ years of progressive, relevant experience, preferably in the pharmaceutical or biotechnology industry. Or equivalent combination of education and experience
• Supervisory/leadership experience required

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)

$78,700.00 - $128,700.00