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Director, Regulatory Affairs - Advertising and Promotion

Company: Abbott Laboratories
Location: Santa Clara
Posted on: November 22, 2021

Job Description:

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.
Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.
Our location in Santa Clara CA , currently has an opportunity for a Director, Regulatory Affairs. The function of a Director Regulatory Affairs is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. Additionally, the individual may develop and supervise regulatory professionals. We are looking for a seasoned regulatory leader ideally with experience in global regulatory operations, advertising & promotional review (ad promo), and pre-market and post-market activities in the medical device industry. The individual has division level influence and is generally considered a key opinion leader and an expert resource both within Abbott and externally. The individual may influence changing regulations and guidance, interface with outside regulatory agencies and trade associations and provide executive management with regulatory metrics/information. The individual may plan, direct, coordinate and control the regulatory affairs activities related to products worldwide.

  • Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
  • Identify need for new regulatory policies, processes and SOPs and approve them.
  • Develop and advance the organization's policy and procedures for regulatory affairs and compliance to establish a compliant culture.
  • Anticipate regulatory and related obstacles and emerging issues throughout the product lifecycle.
  • Analyze and compare regulatory outcomes with initial product concepts and recommend future strategies and actions.
  • Develop global regulatory strategies and update based upon regulatory changes.
  • Conduct regulatory due diligence for potential and new acquisitions and advise management.
  • Sets quality and accuracy standards.
  • Anticipate emerging issues and develop solutions to them.
  • Develop solutions to address issues with other members of management and stakeholders.
  • Create and develop product positioning strategies based upon regulatory requirements.
  • Integrate regulatory considerations into the corporation's global product entry and exit strategy.
  • Recruit, develop, and mentor regulatory professionals.
  • Provide guidance for resource and development planning.
  • Participate in applicable trade association/industry working groups to influence policy/rule-making in alignment with business strategies.
  • Premarket: Communicate application progress to internal stakeholders. Negotiate with regulatory authorities during the development and review process to ensure submission approval. Provide strategic input and technical guidance on regulatory requirements to development teams. Ensure preapproval compliance activities are completed. Formulate company procedures to respond to regulatory authority queries.
  • Postmarket: Oversee regulatory aspects of business relationships to ensure compliance and protect corporate interests. Ensure a system is in place to manage access to information requests. Provide regulatory input for follow-up to inspections and audits to minimize potential for findings of noncompliance. Ensure crisis management program implemented and functioning. Identify and present option for risk mitigation to decision makers. Represent regulatory affairs in product recall and recall communication process. Ensure adverse events are reported to regulatory agencies and internal stakeholders. Manage processes involved with maintaining annual licenses, registrations, listings and patent information. Ensure compliance with product postmarketing approval requirements.
  • Review and approve advertising and promotional items to ensure regulatory compliance.
  • Review and approve publicly disseminated information to minimize regulatory exposure. review product claims, and preserve confidentiality of applicable product information
  • Job specific responsibilities may include (choose applicable areas and expand as appropriate). Medical writing Advertising and promotion. Labeling. Controlled substances (e.g. DEA). Restricted substances (e.g. REACH). Compendial / standards. Import / export. Country specific regulatory support.
  • Must assure that all deadlines are met and provide effective leadership without direct authority. Completed work is checked through consultation and agreement with others rather than by formal review of superior.
  • ork is performed without appreciable direction and exercises significant latitude in determining technical objectives of assignments; assignments are often self-initiated; determines and pursue courses of action necessary to obtain desired results. Individual is recognized as a key opinion leader and resource in regulatory affairs.Influence/Leadership: Develops, communicates, and builds consensus for operating goals that are in alignment with the division and corporation. Provides leadership by communicating and providing guidance towards achieving department, division and/or corporate objectives. Interfaces with a variety of management levels including senior management on significant matters, often requiring the coordination of activity across organizational units. May lead a project team or initiative within department or cross-functions/divisions. Provides technical leadership to business units. Acts as a mentor to less-experienced staff internal and external to the department/division. Exercises judgment independently. Leads assigned departments by developing, communicating, and building consensus for goals and programs that support division, business unit and company objectives. May participate / lead external industry working groups to influence advocacy in alignment with business strategies. Planning/Organization: Creates mid- to long-range plans to carry out objectives established by top management. Develops and calculates a budget for one or more departments to meet organizational goals. Forecasts future departmental or group needs including human and material resources and capital expenditures. Determines and establishes organizational structure and supervisory relationships subject to top management approval.
    Decision Making/Impact: Assignments are expressed in the form of objectives. Work is performed without appreciable direction. Makes decisions regarding work processes or operational plans and schedules in order to achieve the program objectives established by senior management. Consequences of erroneous decisions or recommendations would normally include delays and modifications to projects or operations with substantial expenditure of time, human resources, and funds, and may jeopardize future business activity.
    • Bachelors Degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields OR an equivalent combination of education and work experience.
    • 7-10 years experience in a regulated industry (e.g., medical products, nutritionals). 7-10 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.
    • Regulatory history, guidelines, policies, standards, practices, requirements and precedents --- Regulatory agency structure, processes and key personnel --- Principles and requirements of applicable product laws --- Submission/registration types and requirements --- GxPs (GCPs, GLPs, GMPs) --- Principles and requirements of promotion, advertising and labeling --- International treaties and regional, national, local and territorial trade requirements, agreements and considerations --- Domestic and international regulatory guidelines, policies and regulations --- Ethical guidelines of the regulatory profession, clinical research and regulatory process.
    • Technical/Business Knowledge: --- Monitor costs of projects and of human and material resources within a department or unit --- Monitor company-wide indicators such as market share and profitability --- Develop least cost, least time means to provide optimal regulatory support for new products --- Monitor external environment in area of technical or professional responsibility --- Direct and manage the preparation of technical strategic regulatory documentation for agency submission. --- Understand of reimbursement.
    • Communication Skills or Ability to: --- Communicate effectively verbally and in writing --- Communicate with diverse audiences and personnel --- Write and edit technical documents --- Work with cross-functional teams --- Work with people from various disciplines and cultures --- Write and edit technical documents --- Ability to prepare and present written and oral reports and other presentations to internal and external audiences..... click apply for full job details

Keywords: Abbott Laboratories, Santa Clara , Director, Regulatory Affairs - Advertising and Promotion, Advertising , Santa Clara, California

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