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A career at Resilience is more than just a job – it’s an opportunity to change the future.

Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

For more information, please visit www.resilience.com

Resilience is looking for an attorney with significant commercial contracting and deal management experience in the life sciences industry to support its diverse array of transactions with customers, strategic partners, innovators, and academic institutions. Key to this role are strong fundamentals in the areas of contract drafting, negotiation and deal management; an ability to analyze and synthesize complex matters into concise verbal and written communications; and the provision of strategic and timely advice to key decision-makers. The ideal candidate will have significant experience in negotiating pharma or biopharma manufacturing services and supply agreements and a working understanding of one or more of the following modalities: gene therapies, cell therapies, nucleic acids, vaccines and biologics.

Responsibilities

• Serve as legal counsel to Resilience’s Commercial Teams, helping to build and sustain Resilience’s relationships with customers, strategic collaborators and technology partners.
• Work closely with the heads of Resilience’s various franchises to structure and negotiate agreements for the manufacture and supply of material for research, clinical trials and commercial sale.
• Draft, review and advise on all matter of business agreements relating to the establishment, expansion or change in customer relationships, such as customer proposals, letters of intent, term sheets, project agreements and change orders.
• Draft, review and negotiate a variety of commercial agreements typical for the biotech and pharmaceutical manufacturing industry.
• Support planning and procurement strategies to meet the needs of customers efficiently and effectively.
• Support the integration of new manufacturing facilities into the Resilience network, including due diligence, implementation of network policies and procedures, and updating of form agreements.
• Develop strong understanding of the various proprietary services and manufacturing technologies under development by Resilience and its collaborators and cooperate with IP counsel to consistently implement the company’s IP strategy across all contractual relationships.
• Develop, share, and deploy knowledge and best practices for working with customers, strategic collaborators and innovators.
• Manage outside counsel to ensure timely and knowledgeable support of critical deals.
• Provide additional legal support on other matters and assume other responsibilities, as assigned, including but not limited to general support of the company’s other contracting matters.

Minimum Qualifications :

• Juris Doctorate and Bar admission
• Scientific background
• Significant experience advising on, drafting and negotiating GMP manufacturing agreements for the supply of clinical and commercial quantities of drug substance and/or drug product and other complex agreements involving scientific subject matter and/or intellectual property (including licensing, collaboration, and/or other corporate or commercial transactions).
• Excellent legal drafting and analytical skills required.
• Detail-oriented, organized, efficient, and resourceful with strong follow-through skills.
• Business-minded and practical in addressing legal issues.
• Impeccable professional ethics, integrity, and judgment.
• Strong computer skills, including MS Word, PPT, Excel, and Litera.

Preferred Qualifications:

• Large law firms and prior in-house experience.
• 5 years of relevant experience in Life Sciences industry, including manufacturing.
• Advanced degree or equivalent combination of education and scientific experience in the areas of biotechnology, bioengineering, biological chemistry, gene therapy or cell therapy.
• Ironclad experience.
• Thrive working on a team in a fast-paced environment with priorities that frequently change and occasionally compete.
• Great communicator and solid project manager, able to effectively prioritize and advance many deals happening simultaneously, often under time pressure.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.

Resilience offers employees a robust total rewards program including equity, an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $180,000.00 - $240,000.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.