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Lead Specialist, Safety Vigilance

Stryker

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Stryker

Lead Specialist, Safety Vigilance

Onsite Tokyo, Japan Full Time Mid-Level
Posted 5 months ago
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Job Details

Key Areas of Responsibility:

  • Develops and implements processes involved with maintaining annual licenses, registrations, and listings
  • Reviews and approves advertising and promotion to ensure regulatory compliance
  • Assures post-market regulatory requirements are met (e.g. required reports, supplemental submissions and other post-marketing commitments)
  • Submits notifiable changes and supplemental dossiers to the appropriate regulatory authorities to update product information and/or instructions for use to reflect current state of product knowledge
  • Participates in implementation of regulatory strategy and processes for handling recalls and communication to stakeholders (e.g. HCP, patient, distributor, and health authorities)
  • Reports product safety issues to regulatory authorities as required, to comply with local, regional, and global regulations
  • Provides required information in support of product reimbursement requests
  • Provides regulatory input and appropriate follow-up for inspections and audits
  • Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies
  • Evaluates the regulatory environment and contributes to providing internal advice throughout the product lifecycle (e.g., concept, development, manufacturing, marketing) to ensure product compliance
  • Anticipates regulatory obstacles and emerging issues throughout the product lifecycle and develops solutions
  • Identifies requirements and potential obstacles for market access distribution (federal, provincial/territorial state, reimbursement, purchasing groups, etc.)
  • Assists in the development of regulatory strategy and updates strategy based upon regulatory changes
  • Evaluates proposed products for regulatory classification and jurisdiction
  • Determines requirements (local, national, international) and options for regulatory submission, approval pathways, and compliance activities
  • Provides regulatory information and guidance for product development and planning throughout the product lifecycle to the regulatory groups and others within the organization
  • Compares regulatory outcomes with initial product concepts and recommends changes or refinements based on initial regulatory outcomes
  • Negotiates with regulatory authorities throughout the product lifecycle
  • Identifies the need for new regulatory procedures, SOPs, and participates in development and implementation
  • Helps train stakeholders on current and new regulatory requirements to ensure organization-wide compliance
  • Assists other departments in the development of SOPs to ensure regulatory compliance

Education / Work Experience:

  • BS in Engineering, Science, or related degree; or MS in Regulatory Science                 
  • Typically a minimum of 4 years' experience
  • MS or RAC(s) preferred

Knowledge / Competencies:

  • Strong project management, writing, coordination, and execution of regulatory items
  • Emphasis on technical and scientific regulatory activities
  • Demonstrate knowledge and skills in areas such as regulatory pathways, risk-benefit analysis, communication and collaboration internally and externally, submission, registration, obtaining approval, documentation, compliance, post-marketing surveillance/vigilance and distribution
  • Under general supervision, plans, conducts and supervises assignments
  • Reviews progress and evaluates results
  • Recommends changes in procedures
  • Operates with appreciable latitude for unreviewed action or decision
  • Reviews progress with management
  • May direct work of Specialist or Sr. Specialist
  • Seeks out diverse ideas, opinion, and insights and applies them in the workplace
  • Connects and relates well with people who think and act differently than oneself
  • Embraces scrutiny and accepts feedback as opportunity to learn and improve
  • Chooses the best alternative to achieve desired outcome or effect, giving consideration to risks, tradeoffs, timing, and available resources
  • Navigates the dynamics, alliances, and competing requirements of the organization or business
  • Willingly accepts challenging assignments and new career opportunities that stretch and build capabilities
     
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Required Skills
  • regulatory compliance
  • regulatory strategy
  • regulatory intelligence
  • product lifecycle
  • market access
  • regulatory submission
Company Details
Stryker
 Kalamazoo, MI, United States
Work at Stryker

Stryker is a global leader in medical technologies and, together with our customers, we are driven to make healthcare better. We offer innovative... Read more

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