Director
Biotech & Pharmaceuticals

N/A

Associate Director, Shared Services Delivery Model (SSDM) Regulatory Oversight Lead, Regulatory Affairs International

Merck Sharp & Dohme
Bogota

2 years ago

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The SSDM Associate Director role reports to the SSDM (Sr) Director and will partner cross functionally within GRACS and cross divisionally where applicable to ensure the regulatory post-approval operations in scope of SSDM (i.e.: Renewals, Deletions, Mergers, Acquisitions, Transfers, Legal Entities changes, Site name changes, Tender Bids, CPPs, ancillary documents and artwork implementation) are planned, managed, and executed timely and accurately, issues are identified and resolved, and opportunities for improvement of the business processes are pursued.

  • Manages the selected business processes by providing governance, leadership, and end-to-end support (critical business decisions, changes that affect business processes, roles, and responsibilities)
  • Serve as the point of contact and acts as a resource for process(es) design and performance.
  • Interprets and applies process objectives and performance metrics (establishing a baseline and trending), monitors and reports process performance against metric targets.
  • Ensures process documentation updates and periodic revisions.
  • Supports training, education, knowledge sharing and communication activities for the process.
  • Assess regularly the E2E process and lead or contribute to improvement or re-engineering/ simplification of the business process and related tools.
  • Maintains an effective interface with other relevant cross-functional and cross-divisional processes.
  • Represents Regulatory in cross functional/divisional projects for the regulatory planning and implementation of Marketing Authorizations Transfers (MATs), legal entity changes, site name changes, mergers & acquisitions, and advice/facilitates product transition plans execution in close cooperation with country regulatory affairs.
  • Performs necessary impact assessments on the regulatory information, collects and analyses regulatory intelligence that is required to develop a regulatory transition strategy and integrates it into cross-divisional planning.
  • Identifies and reports regulatory risks.
  • Drives and oversees regional scheduling and planning activities, ensures high level accuracy, and minimizes disruptions by overseeing the connections between the different stakeholders.
  • Secure continuous follow-up & interaction with RAI stakeholders on execution status and on tracking milestones’ achievements of the project plans.
  • Manages the ongoing GRACS-Partner relationship with a focus on overall service delivery, issue management, resolution, and escalation, change management.
  • Defines and tracks the performance of the functional activities and service level targets by the Partner.
  • Maintain close and seamless working relations with the other members of the RAI community, RAI HQ teams, Regional and Country teams, Regulatory Operations, and Information Management teams and GRACS functional teams operating in the international space.
  • This position will manage a team of regulatory professionals.

Required Qualifications/Experience:

  • Bachelor’s degree in life science, engineering, business or a related field (ideally pharmaceutical science degree)
  • Master’s degree (desired)

Requirements

  • Minimum 5-7 years’ experience in pharmaceutical industry
  • Previous experience in Regulatory Affairs, CMC, compliance management or Quality, working with external partners and/or dealing directly with regulatory agencies is preferred.
  • It is recognized that this role will require knowledge of the business and organizational set-up, broad-range experience within and outside of Regulatory Affairs, understanding of Operational Excellence principles, ability to work through the matrix approach in a culturally diverse environment, learning agility, resilience, and emotional intelligence.
  • Good organizational skills with a proven ability to simultaneously balance diverse activities for multiple projects.
  • Strong interpersonal/communication skills and capacity to work across the geographies with the high number of stakeholders.
  • Detail oriented, problem solving, ability to accelerate the decision-making process, project management skills (providing guidance to others in task completion and on-time deliverables)
  • People management (desired)
  • Ability to communicate effectively, both verbally and written, with others across all levels of the organization
  • Ability to work in a matrix organization.
  • Technology proficient; Interest in new tools or automatization will be needed.
  • Innovative mindset and design thinking skills.
Salary
$
77011
-
$
236290
Responsibility
Scope
-
Workplace
-
Functions
Level
N-1
Travel
5%
Date Added
01-10-2024

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