Director, EHS External Manufacturing at Bristol-Myers Squibb

Lawrence Township, 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

Pharmaceuticals, Biotechnology, ManufacturingIndustries

Requirements

Proven track record in EHS at a global scale
Experience driving continuous improvement
Ability to create a safety-first mindset
Forward-thinking leadership skills

Responsibilities

Lead the development and execution of the company’s EHS strategy for external development & manufacturing and approach to TPS EHS Assessments, ensuring alignment with business objectives and regulatory requirements
Further develop and enhance EHS policies and standards to define scope, expectations, roles & responsibilities, and provide a structured process for all stages of the TPRM lifecycle for TPS
Ensure the TPRM program provides a structured process for identifying, assessing, and proactively mitigating EHS risks; communicating and escalating significant/critical risks; and reporting relevant TPS risks for informed decision making
Lead the TPS EHS due diligence and assessment program as part of new supplier selection/RFP process and periodic assessment of existing suppliers
Ensure EHS requirements and performance expectations are clearly defined in TPS contracts and service agreements during new contract awards/renewals with Procurement
Establish a governance structure and reporting process with stakeholders to oversee TPS EHS risks, monitor process metrics/KPIs and trends, and escalate issues
Leverage digital platforms, AIT tools, and data-driven insights & feedback to improve process efficiency, refine program and EHS goals, and drive continuous improvement in EHS performance across the TPS network
Support process to co-ordinate interactions of associated BMS functions (e.g., Product Stewardship, Product Accountability & D)

Skills

EHS

Third-Party Risk Management

TPRM

Regulatory Compliance

Global Supply Chain

Procurement

Product Stewardship

Leadership

Stakeholder Management

Risk Assessment

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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