Legal Counsel

Bora Pharmaceuticals•Maple Grove, MN

1d•Hybrid

About The Position

The Upsher-Smith Legal Counsel will provide strategic, proactive legal counsel to ensure compliant growth and risk management across the organization. This role enables the business to execute commercial strategies while meeting U.S. and global regulatory requirements. This position will be onsite/hybrid with residency in the Twin Cities metropolitan area. Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Bora Pharmaceuticals is focused on developing and manufacturing branded, generic and over the counter (OTC) healthcare and pharmaceutical products for patients around the globe. At Bora Pharmaceuticals, we see it as our mission and our duty to make our mutual success more certain. As an ambitious, future-focused company, we know better than most that our own success is shaped by our partners victories. At Bora, our values guide everything we do — from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone.

Requirements

A Juris Doctor (JD); admitted to practice in Minnesota.
10 years of legal experience in the pharmaceutical, healthcare or medical device industry.
3 years In-House counsel experience.
Experience with commercial litigation and litigation strategy.
Technical expertise in contracts, promotional review, pricing/market access, HCP engagements, distribution/trade, and compliance frameworks.
Business-oriented judgment, negotiation excellence, stakeholder management, crisp written/oral communication, and project prioritization.
Track record of collaborating well with cross-functional colleagues.
Knowledge and ability to understand and apply laws and regulations; ability to analyze a situation and generate solutions.

Nice To Haves

Prior experience with generics and branded pharmaceuticals.
Experience with pre-launch commercialization, generic and rare specialty products.
Familiarity with global frameworks (e.g., HIPAA/Privacy, transparency regimes).
Exposure to digital and field sales promotion (social media, field CRM enablement, speaker programs, congresses) within regulated constraints.
Experience with supply chain, distribution and other 3rd party agreements.
Experience working in a global organization.

Responsibilities

Draft, review, and negotiate: Sales & Distribution agreements (wholesalers, GPO’s, drug chains, specialty distributors, 3PLs) Market access agreements (rebate, chargeback, payer contracting) Promotional services (agencies, speakers bureaus, MSL collaboration boundaries) CDAs and the management of USL and 3rd Party confidential information Vendor MSAs/SOWs, HCP consulting and advisory agreements, event sponsorships Patient support program agreements (hubs, copay vendors, affordability programs) Supply Chain (supply agreements, manufacturing agreements) Purchase agreements including acquisition and divestiture agreements Licensing and Development Agreements including external drug development and co-development agreements; Strategic Partnership Agreement
Maintain contract playbooks and clause libraries; align with Finance and Compliance.
Serve as legal reviewer on Drug Promotion Review Team for claims substantiation, fair balance, use of real-world evidence, social/digital campaigns, and field tools.
Ensure alignment with FDA/FTC guidelines, product labeling, and risk communications.
Provide training to assure legal and regulatory compliance anti-trust, foreign and domestic anti-corruption laws, government programs including Medicare/Medicaid, FDCA, DSCSA, PDMA, Sunshine Laws, and other applicable state and federal laws, regulations and industry guidelines applicable to the Company and its Affiliates.
Interpret and operationalize False Claims Act, Sunshine Act/Open Payments, state marketing codes, and privacy requirements impacting commercial activities.
Partner with Director of Compliance to Advise on HCP interactions, meals/sponsorships, grants & donations, speaker programs, and field force conduct.
Partner with Director of Compliance to update policies, SOPs, and monitoring plans.
Work with, or oversee the work of the Legal Affairs.
Review pricing strategies, rebate structures, patient affordability programs, and value-based contracting (as applicable).
Support trade strategy: GPO/IDN contracting, Retail/Wholesale GPO’s, specialty pharmacy agreements, chargeback/reconciliation frameworks.
Lead internal fact-finding for commercial incidents, coordinate outside counsel for disputes, general litigation or regulatory inquiries.
Oversee and manage general litigation activities including counsel selection, budgeting, litigation strategy, document production and interactions with outside counsel.
Manage legal holds, document preservation, and remediation plans.
Deliver onboarding and periodic training for Commercial teams.
Establish governance cadence (monthly risk reviews, quarterly policy updates) with Commercial leadership.
Recognize and anticipate a wide, and broad, variety of legal issues and business risks; communicate Company leadership the nature of issues and risks and recommend remediation plans.
Develop legal and business strategies with respect, or in response, to proposed business opportunities, legal developments and proposed legislation.
Stay abreast of and communicate industry laws, legal matters and regulations that impact strategy and business operations.
Responsible for maintaining a positive corporate legal posture and advising the leadership team on risk management.