New York State Insurance Fund
Executive Director, Legal Counsel,M&A
New York State Insurance Fund, Trenton, New Jersey, United States,
Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women’s health. Our first Research and Development facility in the US is located in Coral Springs, Florida which focuses on generic and branded orally inhaled and nasal drug products. Somerset, New Jersey is home to one of Fifteen commercial manufacturing sites globally and the only commercial manufacturing facility in the United States for Lupin, as well as additional Research and Development teams. Lupin is prided on being people-focused and centered around how impactful we are with our customers. Dollars are not a measure of success but rather the people we help along the way.
ResponsibilitiesPurposeThe purpose of this role is to drive the strategic & business planning function for the US Generics business, through ongoing assessment and forecasting of key assets, help de-risk key assets, accelerate approvals for complex programs, assist with launch planning of these key assets, and lead integrated efforts for assuring the delivery of the strategic plan for the US Generics business.
Role And ResponsibilitiesLead strategic transactions for the Company, including leading negotiations for corporate M&A and complex licensing and collaboration transactions.Structure, draft, and negotiate complex transactional agreements related to the same.Manage internal and external deal processes and drive deal execution (including form documentation).Plan, assist, and coordinate due diligence exercises as needed. The majority of transactions will focus on the United States market; however, the targeted geographies include Canada, Europe, Mexico, Brazil and other Latin American countries.Led the drafting of general corporate contracts – drafting, negotiating, and reviewing a wide variety of corporate contracts, including confidentiality, consulting, services, manufacturing, clinical trial, basic licensing, and related agreements.Work closely with Business Development, Finance/Accounting, Commercial, and Specialty Businesses to assist in their day-to-day operations/functions.Research, report and recommend corporate actions based on applicable laws and regulations affecting company projects, deployments, business development, accounting, tax, facilities, and administration.Review and revise company policies and procedures as required by applicable law and regulations, and internal requirements.Support Senior Vice President – Legal Affairs in other tasks, including review and negotiation of lender and other strategic agreements.Advise senior management and business personnel, as required.Assist with regulatory and other legal pharmaceutical compliance matters, as required.Manage outside advisors, including active management of outside counsel.Scope and Size
Direct reports: None.Geographic coverage: US.Success Metrics
Feedback from key business stakeholders in Technical, Regulatory, and Commercial teams.Timely approval of key assets / complex products.Successful launch of key assets – timelines, sales, etc.Quality of support provided towards business development.Stakeholder Network
Internal: R&D teams (Americas and EMEA), Commercial, Regulatory, Supply chain, Somerset site leadership team, etc.External: Customers (Retail chains, Wholesalers, GPOs / Hospitals, etc.), R&D consultants, Business partners, FDA, etc.Qualifications
JD degree from an ABA-accredited law school with strong academic credentials.BA/BS from an accredited institution.Ten years of law firm and/or in-house, pharmaceutical legal experience.Member of at least one state bar.Candidates must be able to demonstrate a robust understanding of pharmaceutical business transactions and regulatory issues, intellectual property law, licensing, and mergers and acquisitions.Will be responsible for leading in-licensing, out-licensing, and acquisitions of the company.Experience and familiarity with foreign jurisdictions, especially Europe, is a plus.Awareness of Federal and State healthcare laws and regulations, including Medicare, Anti-kickback, Antitrust.Excellent communication skills (both verbal and written).History of self-motivation, sound judgment, and excellent interpersonal relations.The position requires initiative, responsibility, creativity, motivation, flexibility, and the ability to work independently with minimal supervision.Experience with drafting and negotiating M&A documents, commercial contracts, and pharmaceutical licensing agreements.Ability to communicate effectively with a variety of constituents including executive management, company associates, outside counsel, outside organizations, and agencies.Demonstrate broad business orientation and ability to quickly establish credibility as an attorney and business partner with a cross-functional perspective.Responsiveness and adaptability.Integrity and strong ethics.Ability to travel periodically as needed.Willingness and interest in learning and continuing to develop one’s career and skills.Lupin
is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran’s status, or any other classification as required by applicable law.#J-18808-Ljbffr
ResponsibilitiesPurposeThe purpose of this role is to drive the strategic & business planning function for the US Generics business, through ongoing assessment and forecasting of key assets, help de-risk key assets, accelerate approvals for complex programs, assist with launch planning of these key assets, and lead integrated efforts for assuring the delivery of the strategic plan for the US Generics business.
Role And ResponsibilitiesLead strategic transactions for the Company, including leading negotiations for corporate M&A and complex licensing and collaboration transactions.Structure, draft, and negotiate complex transactional agreements related to the same.Manage internal and external deal processes and drive deal execution (including form documentation).Plan, assist, and coordinate due diligence exercises as needed. The majority of transactions will focus on the United States market; however, the targeted geographies include Canada, Europe, Mexico, Brazil and other Latin American countries.Led the drafting of general corporate contracts – drafting, negotiating, and reviewing a wide variety of corporate contracts, including confidentiality, consulting, services, manufacturing, clinical trial, basic licensing, and related agreements.Work closely with Business Development, Finance/Accounting, Commercial, and Specialty Businesses to assist in their day-to-day operations/functions.Research, report and recommend corporate actions based on applicable laws and regulations affecting company projects, deployments, business development, accounting, tax, facilities, and administration.Review and revise company policies and procedures as required by applicable law and regulations, and internal requirements.Support Senior Vice President – Legal Affairs in other tasks, including review and negotiation of lender and other strategic agreements.Advise senior management and business personnel, as required.Assist with regulatory and other legal pharmaceutical compliance matters, as required.Manage outside advisors, including active management of outside counsel.Scope and Size
Direct reports: None.Geographic coverage: US.Success Metrics
Feedback from key business stakeholders in Technical, Regulatory, and Commercial teams.Timely approval of key assets / complex products.Successful launch of key assets – timelines, sales, etc.Quality of support provided towards business development.Stakeholder Network
Internal: R&D teams (Americas and EMEA), Commercial, Regulatory, Supply chain, Somerset site leadership team, etc.External: Customers (Retail chains, Wholesalers, GPOs / Hospitals, etc.), R&D consultants, Business partners, FDA, etc.Qualifications
JD degree from an ABA-accredited law school with strong academic credentials.BA/BS from an accredited institution.Ten years of law firm and/or in-house, pharmaceutical legal experience.Member of at least one state bar.Candidates must be able to demonstrate a robust understanding of pharmaceutical business transactions and regulatory issues, intellectual property law, licensing, and mergers and acquisitions.Will be responsible for leading in-licensing, out-licensing, and acquisitions of the company.Experience and familiarity with foreign jurisdictions, especially Europe, is a plus.Awareness of Federal and State healthcare laws and regulations, including Medicare, Anti-kickback, Antitrust.Excellent communication skills (both verbal and written).History of self-motivation, sound judgment, and excellent interpersonal relations.The position requires initiative, responsibility, creativity, motivation, flexibility, and the ability to work independently with minimal supervision.Experience with drafting and negotiating M&A documents, commercial contracts, and pharmaceutical licensing agreements.Ability to communicate effectively with a variety of constituents including executive management, company associates, outside counsel, outside organizations, and agencies.Demonstrate broad business orientation and ability to quickly establish credibility as an attorney and business partner with a cross-functional perspective.Responsiveness and adaptability.Integrity and strong ethics.Ability to travel periodically as needed.Willingness and interest in learning and continuing to develop one’s career and skills.Lupin
is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion, age, disability, veteran’s status, or any other classification as required by applicable law.#J-18808-Ljbffr