Spvr Quality Control

Regeneron Pharmaceuticals, Inc (USA)

City of Rensselaer (NY)

Sur place

USD 79 000 - 129 000

Plein temps

Il y a 2 jours
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Avantages offerts par ce poste

annual bonuses or other incentivePlans
equity awards
pension or retirement benefits
401(k) company match
health and wellness programs
fitness centers
insurance benefits (e.g. medical, etc)

Résumé du poste

Regeneron Pharmaceuticals, Inc (USA) seeks a QC Supervisor to lead the QC Drug Product Packaging team on-site in Rensselaer, NY. You will provide front-line support for lab activities supporting testing and release of Drug Product Packaging and Medical Device Components.

You will supervise staff, review protocols, and ensure cGMP compliance while coordinating with QA and manufacturing. Excellent leadership and GMP experience are essential.

Qualifications

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

Responsabilités

  • 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 assay troubleshooting.
  • Performs personnel management functions including schedules and evaluations.
  • Writes and revises SOPs, methods, protocols, and reports.
  • Oversees daily operation of area activities.
  • Supports internal and regulatory audits.
  • Ensures proper training and safety standards.

Connaissances

Supervisory experience
Quality control
GMP experience
Project management

Formation

BS/BA in Life Sciences or related field
MS preferred

Description du poste

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.

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.

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 troubleshooting 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

Required: 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 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.

Salary Range (annually) $78,700.00 - $128,700.00.

Benefits
  • 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
  • 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/.

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.

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.

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician‑scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA‑approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.

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