MSD GRACS Operations Process & Systems OPS Hub Site Lead 

Cuba, Havana 

713495045

Job Description

The GRACS Operations, Process & Systems (OPS) Hub Site Lead role is responsible for (1) establishing and expanding the local GRACS OPS capabilities in coordination with OPS Functional Areas and (2) managing Regional Regulatory Operations staff located at the site execution regulatory operations activities (e.g. submissions planning & execution along with labeling and artwork coordination activities)

• OPS Site leadership is responsible for ensuring effective coordination of local site activities across all OPS functional areas. The individual will work closely with various OPS functional areas and collaborate with key stakeholders at global, region and headquarters. The Hub Site Lead is responsible for fostering a high-performing, collaborative, and inclusive environment that enables delivery excellence, innovation, and efficiency across GRACS OPS Hub functions.

• OPS Site Leadership will additionally have direct managerial responsibilities for Regional Regulatory Operations staff located at the hub site. This position will be responsible for executing regulatory operations activities. The role will be involved with assigned operational work e.g. Submission Planning as well as provide local managerial oversight on the execution of Regional Regulatory Operations hub work that encompasses submission planning and execution, and labeling and artwork coordination activities, while serving as the primary interface with internal stakeholders, site-level governance bodies, and functional leaders. The geographical scope of regional regulatory operations activities may support LATAM or other global capabilities with collaboration across local, regional & global stakeholders as needed.

Theinclude, but are not limited to:

O.P.S. Hub Site Lead: In collaboration with HQ and Regional functions, provide overall OPS direction for regulatory operations at the site, aligning local activities with GRACS global, corporate goals, and regulatory requirements.

• Serve as the primary point of contact for GRACS OPS at the Hub site. Serve as the O.P.S. escalation point for Hub-related challenges and support issue resolution within the OPS team.

• Stakeholder Communication

• General Administrative
  : Leads overall site administration by representing GRACS OPS in site-based activities and ensuring coordination across key support functions, including Facilities, IT, EHS, and Legal. Ensure adequate resource planning, office logistics, and local onboarding of new employees. Monitor organizational site metrics and assess opportunities for cross-OPS resource utilization as appropriate. Support Local HR Driven initiatives and ensure OPS practices remain consistent and aligned across different regions.

• Engagement Champion
  : Drives culture, communication, diversity & inclusion, talent development, and employee engagement initiatives to foster a strong, values-driven workplace in alignment with co-locating functions

• Training and Development
  : Implement training programs to ensure that team members are informed of current regulatory standards and best practices. Also, identify training needs across the Hub and support implementation. Promote cross-functional learning and knowledge-sharing.

Regulatory Regional Operations Manager:

• Lead and develop direct line reports at the Hub, creating an environment that fosters professional growth

• Accountable for Individual Work Tasks & Assignments, e.g., Submission Planning, ensuring these tasks are completed on time.

• Operational Execution & Delivery
  : Accountable for ensuring timely execution to high standards for quality & compliance for all RRO deliverables produced at the Hub, some of which will be worked on by the OPS Hub Lead themselves. Contribute to decision-making processes by providing insights and recommendations based on local expertise and operational needs

• Continuous Improvement
  : Drive process efficiency and operational excellence by establishing streamlined workflows for related activities, aligned with global processes and standards.

• Regulatory Compliance
  : Ensure that all regulatory activities comply with relevant laws, guidelines, and policies. This includes overseeing submissions and documentation and ensuring that appropriate inputs are provided to support audits or issue management.

• Talent Management
  : Support performance management and development plans as well as overall engagement for direct reports. Create an inclusive and collaborative work culture that supports engagement and innovation

• Support Regional Leads by providing essential site-related updates, logistical support, and insights into local country operational dynamics.

Education: Bachelor’s degree in a Life Science, Pharmacy, or Engineering-related field required.

• Advanced degree preferred

• A Project Management Professional certification (PMP) or Scrum Master certification (CSM) or a similar certification is preferred

Experience and Skills Required:

• At least 10 years' experience in the pharmaceutical industry, including 2 years in regulatory operations or regulatory affairs.

• 5+ years of experience in people management

• Excellent people management skills

• Strong written and oral communication skills in English.

• Proficient project management skills with the ability to handle multiple tasks and prioritize effectively.

• Very strong negotiation, communication, interpersonal, and reasoning skills

• Excellent presentation skills

• Growth mindset and bigger picture seeking individual

• Tech-savvy professional with Microsoft Suite and Power BI experience

• Demonstrated ability to analyze, define, and solve related problems, and advise functional area leads on managing risks

• Ability to work toward enterprise goals, using influence rather than control, and fostering a work environment based on trust, sharing, and collaboration.

• Ability to collaborate with diverse stakeholders in a variety of project environments

• Team player

• Proactive and action-oriented approach

Current Contingent Workers apply

No Travel Required

Not Indicated

Animal Vaccination, Animal Vaccination, Biopharmaceuticals, Biopharmaceutics, Common Technical Document, Cross-Functional Teamwork, Delivery Excellence, Document Control Systems, Electronic Submissions, Employee Training Programs, Management Process, Medical Device Regulations, Mentorship, Multi-Management, Operational Excellence, Operational Execution, Organization Administration, People Leadership, People Management, Project Management, Regulatory Affairs Compliance, Regulatory CMC, Regulatory Compliance, Regulatory Experience, Regulatory Strategy Development {+ 4 more}

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