Job Description

Your Role As a member of cross-functional teams, you shape the US and global IP strategy for pharmaceutical development projects and commercial products. You will build and defend patent portfolios, manage freedom to operate, and advise on IP provisions in contracts. You are thus responsible for invention harvesting, patent drafting, prosecution, enforcement and invalidation proceedings, as well as legal opinions. Litigation will also be an important aspect of your role. In addition, you will perform IP due diligence on external business opportunities and, as a member of small deal teams, contribute to and negotiate license and other agreements. In your role, you will routinely interact with scientists of our pharmaceutical R&D organization, but also with colleagues from other functions including Regulatory Affairs, Commercial, Business Development and Legal. Providing strategic IP advice to senior leadership is an important aspect of the role. You will join an established international team of patent attorneys with global responsibility. Who You Are Minimum Qualifications: Juris Doctorate from an accredited law school and BA/BS degree in the chemical, biological or pharmaceutical sciences Admitted to at least one State Bar and registered to practice in front of the United States Patent and Trademark Office (USPTO). Gained considerable experience in a patent department in the pharmaceutical or biotech industry or in a law firm. Able to demonstrate patent drafting, prosecution and post-grant proceedings (PGR and IPR), as well as freedom-to-operate (FTO) analyses. Strong communicator and a team player. Experience in advising/counseling colleagues or clients in the healthcare business. Excellent organizational skills. Takes ownership of your work and its impact on our business. Comfortable managing competing priorities without losing sight of either essential details or the big picture. Preferred Qualifications: Litigation experience, more particularly experience in Hatch-Waxman litigation. Experience in due diligence projects and contract negotiation. Possess a sound understanding of the regulatory framework for pharmaceuticals. Location: Billerica, MA; Hybrid preferred; Open to Greater Boston Area Travel: Pay Range for this position: $183,100.00 - $274,700.00 Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses. The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination. #J-18808-Ljbffr Merck Gruppe

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