Senior Director, Associate General Counsel

Job description

Overview

At Pacira, innovation meets purpose.

Pacira BioSciences, Inc. is a pioneer in non-opioid pain management and regenerative health solutions. Today, we’re building on that legacy with next-generation innovations for chronic, postsurgical, and musculoskeletal pain. Our culture is built on collaboration, innovation, and a shared commitment to helping patients recover faster. We are redefining what’s possible in pain management—and we can’t do it without talented people like you.

Why Join Us?

At Pacira, every career is more than a job. Our mission drives us, and every day, we challenge ourselves to achieve the extraordinary. Integrity is at the core of who we are. We value diverse perspectives and the collective strength of a unified team. Join the team in making better possible for patients everywhere.

Summary

The purpose of this position is to support the Chief Legal Officer and Senior Management in managing certain legal functions of the company, with primary substantive responsibility for business development transactions, including M&A, licensing, and partnerships, and supervisory responsibility, strategic oversight, and escalation authority for the broader contracting function.

Essential Duties & Responsibilities

Oversee and take ownership of contracting function for business development transactions and M&A matters, including drafting, reviewing, negotiating, and advising on related agreements and transactions.

Oversee and take ownership of the contracting function and provide strategic direction on contract strategy, process, prioritization, and risk-based decision-making across the full contract group.

Serve as escalation authority for contracting matters handled by the broader contract group, including complex negotiations, non-standard terms, risk assessments, and business-sensitive issues.

Supervise and mentor direct reports to facilitate professional growth; identify training opportunities and provide mentoring to ensure individuals are appropriately developed in accordance with their roles and responsibilities.

Become a strategic partner with Regulatory, Finance, IT, Clinical, Manufacturing, Medical, and Commercial Groups to assist them with their various legal needs.

Review, draft, and implement corporate policies and procedures.

Advise Senior Management on legal issues and risk.

Assist General Counsel on other legal projects on as-needed basis.

Manage outside counsel relationships for transactions and M&A matters, including budgeting, workflow oversight, and quality control of external legal work product.

Supervisory Responsibilities

This position will have supervisory responsibilities.

Interaction

Will work closely with the Chief Legal Officer and customers, vendors, outside counsel and consultants. Business areas supported include: research and development, clinical trials (commercial products and potential pipeline products), medical affairs, market access, corporate communications, global supply chain and quality, manufacturing, commercial sales and marketing to healthcare providers, patients and payers (including U.S. Federal Government), business development, procurement, finance, compliance, and human resources.

Education and Experience

JD and a State Bar admission

Minimum 10 years of major law firm or in-house experience. Three years of in-house experience with a major pharmaceutical and/or biotech company is preferred but not necessary.

Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Knowledge, Skills, and Abilities

Exceptional English communication skills written and verbal, organizational abilities, decision making, and proven attention to detail.

Strong Microsoft Office skills: Word; Excel; Outlook.

Demonstrated ability to work effectively within a team environment.

Demonstrated ability to multi-task and produce quality work product in a fast-paced, stimulating environment.

Demonstrated experience managing or supervising legal professionals or contract specialists is strongly preferred

Experience in licensing, collaboration agreements, M&A transactions, or business development transactions in the life sciences industry

Demonstrated excellent business judgment and the ability to form strong working relationships with internal clients while maintaining adherence to legal standards.

Proven depth of knowledge of corporate legal issues, particular to the pharmaceutical and/or Biotech industry including contracts and compliance.

Ability to travel, sometimes frequently to headquarters in Brisbane, CA, up to 25% of the time.

Physical Demands

The employee is regularly required to travel by automobile as well as by airplane and other forms of public transportation. While performing the duties of this job, the employee is regularly required to sit, talk, move between spaces, reach with hands and arms. Close vision and the need to focus on computer screen, use of hands, fingers, and wrist to type on keyboard and manipulate mouse.

Work Environment

Typical office setting, office will be a cubicle, noise level is moderate with consistent printer, telephone ringing, and conversation. Hybrid work environment and employee is required to work in the Pacira office at least three days a week (no exception).

This position requires regular travel to Brisbane, CA at least once per month.

Benefits

Medical, Prescription, Dental, Vision Coverage

Flexible Spending Account & Health Savings Account with Company match

Employee Assistance Program

Mental Health Resources

Disability Coverage

Life insurance

Critical Illness and Accident Insurance

Legal and Identity Theft Protection

Pet Insurance

Fertility and Maternity Assistance

401(k) with company match

Flexible Time Off (FTO) and 11 paid holidays

Paid Parental Leave

Pay Transparency

The base pay range for this role is $203,000 per year to $267,000 per year. The range is what we reasonably expect to pay for this role. The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications. Depending on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered.

EEO Statement

Pacira is proud to be an Equal Opportunity Employer and does not discriminate against applicants because of race, color, religion, sex (including gender identity, sexual orientation, and pregnancy), national origin, age (40 or older), veteran status, disability or genetic information, or any other characteristic protected under applicable federal, state, or local law. At Pacira we are committed to intentionally cultivating a culture of inclusion where all feel welcomed and valued for their background, perspectives, and experiences. We hold one another accountable to promote trust and transparency in support of our communities and collective purpose.

Agency Disclaimer: Pacira Biosciences, Inc. (Hereafter, Pacira) does not accept unsolicited resumes from recruiters or employment agencies in response to the Pacira Careers page or a Pacira social media post. Pacira will not consider or agree to payment of any referral compensation or recruiter fee relating to unsolicited resumes. Pacira explicitly reserves the right to hire said candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Pacira.

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Who can apply

Review the original listing for work authorization, qualifications and employer requirements.