Regulatory Affairs Manager

1970-01-01Davis Companieshttp://daviscos.com/wp-content/themes/davis_theme/assets/images/logo.svg325 Donald J. Lynch Boulevard, Suite 201MarlboroughMA01752USAcustomer support[+800-482-9494][+508-481-8519]
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Regulatory Affairs Manager

  • Specialty:

    Engineering
    • City:

    • State:

  • Assignment Type:

    Direct Hire
  • Job Id:

    55413
  • Payrate:

    $64.90

Description

Regulatory Affairs Manager, Canton Ma

Job Summary 

The Regulatory Affairs Manager will support regulatory activities for Vaccines Business Unit as the regulatory representative on assigned Product Team(s).  He/she will work with functional line management and team members across multiple disciplines including nonclinical, clinical and CMC to develop regulatory strategies and manage regulatory submission activities. The RA manager will take the lead on regulatory activities, including the management of authoring, review, and coordination of submissions, as well as planning and executing meetings with regulatory agencies.

 

Essential Functions   
•    Represent Regulatory Affairs as the SME on assigned product/ project teams and ensure timely communication of regulatory strategy and plans to team members and line management
•    Develop regulatory strategy for assigned products and/or country
•    Plan and coordinate the preparation of regulatory submissions including meetings with health authorities and routine correspondence
•    Provide critical review of all documentation supporting regulatory applications
•    Provide gap analysis of submissions based on regulatory requirements; anticipate Health Authority responses and communicate areas of risk to project teams and line management
•    Plan, coordinate, prepare and support meetings and teleconferences with regulatory agencies and submission meetings; may also be required to work with government funding agencies
•    Prepare responses to complex questions and comments from regulatory agencies
•    Ensure regulatory product compliance for product (e.g. agency commitments)
•    As required, provide regulatory assessment for deviations, change controls and manage associated regulatory activities to ensure compliance
•    Conduct and analyze regulatory research to understand competitor activity 
•    Interact with company partners and consultants for various regulatory matters as needed
•    As required, develop procedures to support the regulatory affairs department
•    Maintain awareness of new and developing legislation, policy and technical regulatory guidance relating to assigned programs. Interpret existing regulations and guidance documents for regulatory department and/or project teams
•    May be responsible for a functional area and/or have direct reports


The above statements are intended to describe the general nature of work performed by those in this job.  It is not an exhaustive list of all duties, and other duties may be assigned.

 

Minimum Education, Experience, Skills
•    Bachelor’s degree in a life sciences or related discipline required.  Approximately 8+ years of relevant pharmaceutical industry experience, with minimum 5 years in Regulatory Affairs.  Less experience acceptable for suitable candidates with relevant industry experience and skill sets.
•    Must have experience interacting with the FDA, EMA, Health Canada and/or other agencies as required
•    Ability to work on problems of diverse scope
•    Identifies priorities and key issues in complex situations and solves with minimal assistance
•    Exercises judgement within generally defined regulatory practices and policies
•    Experienced in leading cross-functional interactions related to regulatory matters
•    Effective in both written and oral communication
•    Is able to direct work as required and manage complexity
•    Thorough knowledge of the development of one or more types of Health Authority regulated products (drugs, biologics, medical devices, combination products)
•    Ability to anticipate and prevent potential issues
•    Understanding of regulatory issues and their touch points 

There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate.

Reasonable accommodations may be made to enable individuals with disabilities to perform all essential functions.
 

Emergent BioSolutions is an Equal Opportunity/Affirmative Action Employer and values the diversity of our workforce.  Emergent does not discriminate on the basis of race, color, creed, religion, sex or gender (including pregnancy, childbirth, and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, age, national origin, ancestry, citizenship status, marital status, physical or mental disability, military service or veteran status, genetic information or any other characteristics protected by applicable federal, state or local law.
 

Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy .
 

Emergent BioSolutions does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Emergent BioSolutions’ approved agency list. Unsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions’ approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency.

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