Senior Corporate Counsel Quality Law
Bristol-Myers Squibb
Senior Corporate Counsel Quality Law
Job Description
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 Familiarity with Good Manufacturing Practices (GMP) preferable but not required 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 ability to provide clear, operational and effective legal advice that supports informed decisions Lead and organize functional or substantive working groups assessing significant legal issues Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. 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 is critical. Ability to discuss various topics with senior executive leadership is essential for success in this position. The ideal candidate must have excellent verbal and written communication and collaboration skills, be proactive, and be able to prioritize and manage multiple projects and clients. The candidate will operate as part of the Law Department focused on providing excellent, pragmatic, solutions oriented services to clients. Must be highly collaborative with the ability to garner the trust of others, build productive internal and external professional relationships, and operate effectively in a multi-cultural environment. Commitment to a diverse and inclusive workplace is critical. Superior personal integrity and ethics are required.
About the Role/Company
- The candidate will operate as part of the Law Department focused on providing excellent, pragmatic, solutions-oriented services to clients
Key Responsibilities
- Proactively advise and counsel clients in the Global Quality organization
- Provide strategic legal and regulatory advice across a diverse range of product categories, including small molecule, cell therapy, biologics, and medical devices
- Provide transactional legal support
- 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
- Provide clear, operational, and effective legal advice that supports informed decisions
- Lead and organize functional or substantive working groups assessing significant legal issues
Required Qualifications
- 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)
- Superior personal integrity and ethics
Preferred Qualifications
- Familiarity with Good Manufacturing Practices (GMP)
Skills Required
- 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 approach
- Ability to prioritize and manage multiple projects and clients
- Highly collaborative with the ability to garner the trust of others
- Ability to build productive internal and external professional relationships
- Ability to operate effectively in a multi-cultural environment
- Commitment to a diverse and inclusive workplace
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
Locations
- Princeton NJ, United States
Salary
Estimated Salary Rangemedium confidence
180,000 - 250,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to navigate complex legal issues while exhibiting sound judgment and objectivityintermediate
- Strong attention to detailintermediate
- Ability to discuss various topics with senior executive leadershipintermediate
- Excellent verbal and written communication and collaboration skillsintermediate
- Proactive approachintermediate
- Ability to prioritize and manage multiple projects and clientsintermediate
- Highly collaborative with the ability to garner the trust of othersintermediate
- Ability to build productive internal and external professional relationshipsintermediate
- Ability to operate effectively in a multi-cultural environmentintermediate
- Commitment to a diverse and inclusive workplaceintermediate
Required Qualifications
- Bachelor's or equivalent degree (experience)
- JD required (experience)
- Qualification, or ability to become qualified to practice in-house in New Jersey (experience)
- Knowledge of, and experience with, pharmaceutical industry and laws (experience)
- Minimum of 10 years of legal experience preferred (law firm, in-house, or government experience) (experience)
- Superior personal integrity and ethics (experience)
Preferred Qualifications
- Familiarity with Good Manufacturing Practices (GMP) (experience)
Responsibilities
- Proactively advise and counsel clients in the Global Quality organization
- Provide strategic legal and regulatory advice across a diverse range of product categories, including small molecule, cell therapy, biologics, and medical devices
- Provide transactional legal support
- 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
- Provide clear, operational, and effective legal advice that supports informed decisions
- Lead and organize functional or substantive working groups assessing significant legal issues
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
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Answer 10 quick questions to check your fit for Senior Corporate Counsel Quality Law @ Bristol-Myers Squibb.
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Senior Corporate Counsel Quality Law
Bristol-Myers Squibb
Senior Corporate Counsel Quality Law
Job Description
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 Familiarity with Good Manufacturing Practices (GMP) preferable but not required 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 ability to provide clear, operational and effective legal advice that supports informed decisions Lead and organize functional or substantive working groups assessing significant legal issues Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. 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 is critical. Ability to discuss various topics with senior executive leadership is essential for success in this position. The ideal candidate must have excellent verbal and written communication and collaboration skills, be proactive, and be able to prioritize and manage multiple projects and clients. The candidate will operate as part of the Law Department focused on providing excellent, pragmatic, solutions oriented services to clients. Must be highly collaborative with the ability to garner the trust of others, build productive internal and external professional relationships, and operate effectively in a multi-cultural environment. Commitment to a diverse and inclusive workplace is critical. Superior personal integrity and ethics are required.
About the Role/Company
- The candidate will operate as part of the Law Department focused on providing excellent, pragmatic, solutions-oriented services to clients
Key Responsibilities
- Proactively advise and counsel clients in the Global Quality organization
- Provide strategic legal and regulatory advice across a diverse range of product categories, including small molecule, cell therapy, biologics, and medical devices
- Provide transactional legal support
- 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
- Provide clear, operational, and effective legal advice that supports informed decisions
- Lead and organize functional or substantive working groups assessing significant legal issues
Required Qualifications
- 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)
- Superior personal integrity and ethics
Preferred Qualifications
- Familiarity with Good Manufacturing Practices (GMP)
Skills Required
- 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 approach
- Ability to prioritize and manage multiple projects and clients
- Highly collaborative with the ability to garner the trust of others
- Ability to build productive internal and external professional relationships
- Ability to operate effectively in a multi-cultural environment
- Commitment to a diverse and inclusive workplace
Benefits & Perks
- Paid national holidays and optional holidays
- Global Shutdown Days between Christmas and New Year's holiday
- Up to 120 hours of paid vacation
- Up to two (2) paid days to volunteer
- Sick time off
- Summer hours flexibility
Locations
- Princeton NJ, United States
Salary
Estimated Salary Rangemedium confidence
180,000 - 250,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to navigate complex legal issues while exhibiting sound judgment and objectivityintermediate
- Strong attention to detailintermediate
- Ability to discuss various topics with senior executive leadershipintermediate
- Excellent verbal and written communication and collaboration skillsintermediate
- Proactive approachintermediate
- Ability to prioritize and manage multiple projects and clientsintermediate
- Highly collaborative with the ability to garner the trust of othersintermediate
- Ability to build productive internal and external professional relationshipsintermediate
- Ability to operate effectively in a multi-cultural environmentintermediate
- Commitment to a diverse and inclusive workplaceintermediate
Required Qualifications
- Bachelor's or equivalent degree (experience)
- JD required (experience)
- Qualification, or ability to become qualified to practice in-house in New Jersey (experience)
- Knowledge of, and experience with, pharmaceutical industry and laws (experience)
- Minimum of 10 years of legal experience preferred (law firm, in-house, or government experience) (experience)
- Superior personal integrity and ethics (experience)
Preferred Qualifications
- Familiarity with Good Manufacturing Practices (GMP) (experience)
Responsibilities
- Proactively advise and counsel clients in the Global Quality organization
- Provide strategic legal and regulatory advice across a diverse range of product categories, including small molecule, cell therapy, biologics, and medical devices
- Provide transactional legal support
- 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
- Provide clear, operational, and effective legal advice that supports informed decisions
- Lead and organize functional or substantive working groups assessing significant legal issues
Benefits
- general: Paid national holidays and optional holidays
- general: Global Shutdown Days between Christmas and New Year's holiday
- general: Up to 120 hours of paid vacation
- general: Up to two (2) paid days to volunteer
- general: Sick time off
- general: Summer hours flexibility
Tags & Categories
Answer 10 quick questions to check your fit for Senior Corporate Counsel Quality Law @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs