Senior Corporate Counsel Quality Law at Bristol-Myers Squibb

Princeton, New Jersey, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, BiotechnologyIndustries

Requirements

Bachelor’s or equivalent degree; JD required
Qualification, or ability to become qualified to practice in-house in New Jersey
Knowledge of, and experience with, pharmaceutical industry and laws
Minimum of 10 years of legal experience preferred (law firm, in-house, or government experience)
Ability to navigate complex legal issues while exhibiting sound judgment and objectivity
Strong attention to detail
Ability to discuss various topics with senior executive leadership
Excellent verbal and written communication and collaboration skills
Proactive, with ability to prioritize and manage multiple projects and clients
Highly collaborative with ability to garner trust, build productive internal and external relationships, and operate effectively in a multi-cultural environment
Commitment to a diverse and inclusive workplace
Superior personal integrity and ethics
Familiarity with Good Manufacturing Practices (GMP) preferable but not required

Responsibilities

Proactively advise and counsel clients in the Global Quality organization
Provide strategic legal and regulatory advice, and transactional legal support, across a diverse range of product categories, including small molecule, cell therapy, biologics and medical devices
Collaborate across business colleagues and Law Department matrix to ensure delivery of seamless, comprehensive legal advice
Anticipate and proactively identify legal issues applying an enterprise view, and provide clear, operational and effective legal advice that supports informed decisions
Lead and organize functional or substantive working groups assessing significant legal issues

Skills

Corporate Law

Quality Law

GMP

Regulatory Compliance

Manufacturing Law

Supply Chain Law

Product Development

EHS

Transactional Law

Small Molecule

Cell Therapy

Biologics

Medical Devices

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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