Supernus Pharmaceuticals, Inc.

Senior Manager Regulatory Affairs CMC

Supernus Pharmaceuticals, Inc.  •  $135k - $155k/yr  •  Rockville, MD (Onsite)  •  5 months ago
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Job Description

The Senior Manager, CMC is responsible for managing the regulatory aspects of projects/products including the preparation and submission of correspondence and applications to regulatory agencies.

Essential Duties & Responsibilities:

  • Identifies, obtains, compiles and reviews regulatory documents concerning CMC-related issues that are needed for FDA submissions including IND, NDA, NDA supplements and briefing packages for agency meetings.
  • Facilitates preparation of IND/NDA annual reports and keep other annual updates or reports current.
  • Review and assess the regulatory impact of routine proposed manufacturing related changes, non-conformance events and other GMP related documents; researches topics when requested by supervisor.
  • Work directly with the contract electronic publisher to get submissions published and submitted.
  • Tracks, documents and communicates progress of regulatory submissions and approvals.
  • Orders, tracks and process CMC-related regulatory submission documentation (e.g. certificates, declarations, sample requests and COAs).
  • With appropriate supervision from senior management, interfaces cross-functionally with CMC stakeholders (e.g. manufacturing, supply chain and quality) in the context of major manufacturing initiatives.
  • Under supervision, evaluate and communicate impact of relevant regional regulations, guidance and current regulatory environment.
  • Other Duties as Assigned.

Supervisory Responsibilities:

  • N/A.

Knowledge & Other Qualifications:

  • Relevant Ph.D. with minimum 3+ years or Master’s/ Bachelor’s with minimum 6+ years relevant experience in pharmaceutical regulatory affairs.
  • Previous experience with global regulatory submissions a plus.
  • Solid knowledge of eCTD Quality sections and regulatory submissions experience.
  • Excellent knowledge and understanding of FDA/ICH regulations and relevant guidance (CMC).
  • Proficient in Microsoft Windows applications.

Other Characteristics:

  • Ability to work independently and as part of a team and maintain high ethical standards of integrity and quality.
  • Ability of having an innovative and dynamic approach to work.
  • A self-starter able to work independently but comfortable working in a team environment.
  • Ability to consistently exhibit Supernus Values in interactions with employees at all levels of the organization, vendors, customers and others.
  • Capable of performing other duties as assigned by Management.
  • Authorized to legally work in the United States without visa sponsorship.

Physical Requirements/Work Environment/Travel Requirements:

  • Sedentary work. Exerting up to 10 pounds of force occasionally and/or carrying objects. Sedentary work involves sitting most of the time.
  • The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer screen, iPad, or other electronic device; and extensive reading.
  • The worker is not substantially exposed to adverse environmental conditions.

Compensation:

At Supernus, we offer a competitive compensation package that reflects your experiences and contributions. The expected salary range for fully qualified candidates applying for this role is $135,000 to $155,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual’s salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.

Base salary is one part of the overall compensation package, which includes the opportunity to participate in employee stock purchase programs and performance-based bonus programs.

Supernus Pharmaceuticals is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, disability, protected veteran status, age or any other characteristic protected by law.

Supernus Pharmaceuticals, Inc.

About Supernus Pharmaceuticals, Inc.

We are a pharmaceutical company focused on developing and commercializing products for the treatment of central nervous system (CNS) diseases. Our extensive expertise in product development has been built over the past 30 years: initially as a standalone development organization, then as a U.S. subsidiary of Shire plc and, in late 2005, as Supernus Pharmaceuticals Inc. We market our products in the United States through our own specialty sales force and seek strategic collaborations with other pharmaceutical companies to license our products outside the United States.

We market Qelbree® (viloxazine extended-release) for the treatment of attention deficit/hyperactivity disorder (ADHD) in children ages 6 to 17. Trokendi XR® (extended-release topiramate) for the prophylaxis of migraine and the treatment of epilepsy, Oxtellar XR® (extended-release oxcarbazepine) for the treatment of epilepsy, Apokyn® (apomorphine hydrochloride injection) for the acute treatment of hypomobility in advanced Parkinson’s disease (PD), Myobloc® (rimabotulinumtoxinB) for the treatment of cervical dystonia and treatment of chronic sialorrhea in adults, and Xadago® (safinamide) as an adjunctive treatment to levodopa/carbidopa in PD patients with hypomobility.

We are also developing several product candidates to address large market opportunities in the CNS market, including SPN-812 for the treatment of ADHD in adults, apomorphine infusion pump for hypomobility in PD, SPN-820 (NV-5138) for treatment-resistant depression, and SPN-817 for the treatment of epilepsy.

Industry
Chemicals & Materials
Company Size
501-1,000 employees
Headquarters
Rockville, Maryland
Year Founded
2005
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