Legal Specialist

MSN Pharmaceuticals Inc.; Piscataway Township (NJ); On-site; USD 90,000 - 150,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Job summary

A pharmaceutical company in Piscataway Township, NJ seeks an entry-level Legal Associate to develop expertise in intellectual property law and ANDA litigation. Responsibilities include analyzing patents, drafting legal documents, and supporting IP due diligence processes. Applicants should have a JD degree and 2 to 8 years of relevant experience. The role requires strong analytical skills and proficiency in legal drafting, offering benefits like medical insurance, vision insurance, and a 401(k).

Qualifications

• 2 to 8 years of experience in ANDA litigation and FDA regulatory law.
• Experience in IP due diligence, settlement and licensing agreements is a plus.
• Experience with IP due diligence, settlements, licensing, deposition, and trial prep is a plus.

Responsibilities

• Conduct detailed analysis of patents and technical documentation.
• Draft and review freedom-to-operate and invalidation opinions.
• Prepare and draft notice letters and statements.
• Contribute to IP due diligence processes for settlements and agreements.
• Support business development by providing IP assessments.
• Collaborate while handling tasks independently.

Skills

Strong analytical skills

Proficient in drafting legal documents

Ability to work independently and in a team

Education

Juris Doctor (JD) degree

Bachelor’s, Master’s, or Ph.D. in Pharmaceuticals or Chemistry

Job description

We are seeking a Legal Associate with foundational experience in intellectual property law and a keen interest in ANDA litigation.

This role is ideal for an entry-level attorney eager to develop their expertise in IP law, working alongside experienced professionals in a dynamic team.

Job Title: Legal Associate – IPM

Key Responsibilities:

• Conduct detailed analysis of patents, file histories, technical documentation, and expert opinions.
• Draft and review freedom-to-operate and invalidation opinions.
• Prepare and draft notice letters and detailed statements.
• Contribute to IP due diligence processes, including preparation for settlements, licensing agreements, depositions, and trial preparation.
• Support business development and research initiatives by providing IP assessments.
• Collaborate effectively within the team while also handling tasks independently as required.

Qualifications:

Educational Background:

• Juris Doctor (JD) degree (US).
• Bachelor’s, Master’s, or Ph.D. in Pharmaceuticals or Chemistry preferred.

Experience:

• 2 to 8 years of experience in ANDA litigation, with a basic understanding of FDA regulatory law.
• Experience in IP due diligence, settlement and licensing agreements, deposition, and trial preparation is a plus.

Skills and Competencies:

• Strong analytical skills with the ability to assess complex patent and technical documents.
• Proficient in drafting legal documents with accuracy and clarity.
• Ability to work both independently and as a collaborative team member.

Note:

• U.S. citizenship or permanent authorization to work in the U.S. is mandatory.
• This job description is not all-inclusive and serves as a guideline. Responsibilities may evolve based on business needs, with additional duties assigned as necessary.
• We are an Equal Opportunity Employer. We welcome applicants from all backgrounds, including minorities, women, veterans, individuals with disabilities, and members of the LGBTQ+ community.

Medical insurance, Vision insurance, and 401(k) are offered.