Senior Manager, GMP Facilities at Bristol-Myers Squibb

Summit, New Jersey, United States

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, PharmaceuticalsIndustries

Requirements

Leadership experience in managing 24/7 Facilities and Maintenance teams in GMP manufacturing environments
Expertise in Safety and Environmental regulations, Good Manufacturing Practices (GMP), Governing Building Codes, and pharmaceutical industry regulations
Ability to develop and implement short- and long-term strategies aligned with site and business objectives
Skills in team development, including hiring, talent development, coaching, and performance management to foster inclusive environments
Knowledge of systems and processes to minimize equipment inconsistencies or defects
Experience implementing and tracking maintenance and reliability KPIs with review processes
Capability to collaborate on reliability strategies ensuring equipment operates per design specifications
Familiarity with predictive analytics for facilities and equipment management

Responsibilities

Member of the Site Safety Committee
Champion safety and compliance within the Facilities & Engineering Department; set expectations and ensure adherence to Safety, Environmental regulations, GMP, Building Codes, and industry regulations
Ensure support structures are in place for compliance; support development of procedures and programs, implement, monitor performance, identify opportunities, and prepare action plans
Set short- and long-term strategies for the team aligned with Facilities & Engineering and Summit West Cell Therapy objectives; communicate clear vision
Develop and manage the team through hiring, talent development, coaching, and performance management in an inclusive environment
Develop and implement systems and processes to minimize inconsistencies or defects in equipment leading to variability
Implement and track best-in-class maintenance and reliability KPIs; ensure review processes to address performance issues
Collaborate with Reliability to define and implement strategies for reliable equipment operation per design specifications
Identify opportunities to implement and utilize predictive analytics (including machine learning)

Skills

Key technologies and capabilities for this role

GMPFacilities ManagementMaintenanceCell Therapy ManufacturingEngineeringTeam LeadershipOperational ReadinessInspection Readiness

Questions & Answers

Common questions about this position

What is the work schedule for this position?

The shift available is Monday - Friday, onsite day shift from 7:30 a.m. - 4 p.m.

Is this role remote or onsite?

This is an onsite position at the Summit West Site.

What are the main responsibilities of this role?

The role involves providing leadership to the 24/7 Facilities and Maintenance team, ensuring GMP facilities and equipment are maintained for operational and inspection readiness, and implementing a strategic plan for efficiency, quality, safety, and environmental protection.

What does the company culture at Bristol Myers Squibb emphasize?

The culture is described as challenging, meaningful, and life-changing, with opportunities to grow alongside high-achieving teams, a focus on balance and flexibility, and a commitment to reimagining cell therapy to help patients.

What benefits does Bristol Myers Squibb offer?

The company offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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