Director, Analytical Team Leader

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership – Leveraging our collective expertise to connect people to products and services.
Every day, we rise to the challenge to make a difference and here’s how the Director, Analytical Team Leader role will make an impact:


Key responsibilities for this role include:

  • Lead the delivery of all analytical activities to take a portfolio of new respiratory products to clinical studies and commercialization
  • As a portfolio lead, support the planning and execution of experiments to generate scientific understanding in development of analytical methods, formulations and processes.
  • Ensure  the  smooth  transfer  of  project  analytical  methodologies  to  Viatris’s  commercial manufacturing facility.
  • Lead the review and approval of data, interpretation of results and reporting of experimental outcomes to project development teams.
  • Ensure that analytical activities carried out within the team with potential impact on quality of clinical supplies or product approval are delivered in accordance with cGMP requirements.
  • As a member of the analytical leadership team, take shared accountability for driving high standards of scientific excellence, cGMP compliance and safety within the Analytical function.  Contribute to strategic business development and management of resources to deliver the project portfolio on time and within budget.
  • Lead scientific input to troubleshooting and investigations.
  • Review  and  approve  documentation  (e.g.  protocols,  reports,  procedures,  specifications)  as required.
  • Lead the delivery of analytical input to investigational and commercial drug product regulatory filings.
  • Take responsibility for performance management and professional development of staff within the team.
  • Lead the improvement of departmental capabilities, e.g. by implementation of new technologies.
  • Adhere to all applicable policies and procedures, including those relating to EHS, GMP, GCP,
  • Quality and Compliance, consistent with the role and any associated responsibilities, including people management where applicable.
  • Shape formulation design and scale up strategies and overall project plans through input and leadership at matrix team technical discussions.
  • Perform other duties as assigned consistent with the grade of the role.


The minimum qualifications for this role are:

  • Has substantial experience of the application of analytical chemistry to product development, including practical experience of modern laboratory techniques (e.g. drug product testing, API characterisation).
  • Has  substantial  experience  in  the  management  of  analytical  activities  to  achieve  project deliverables.
  • Has substantial experience in performance management and personal development of others.
  • Has   substantial   experience   in   authoring   GMP   documentation   and   preparing   regulatory submissions
  • Has substantial experience of the challenges involved in the validation and transfer of complex analytical methods to commercial facilities
  • Able to lead the interpretation of complex data to solve product development issues.
  • Able to proactively identify and address barriers to collaborative working with internal and external partners.
  • Able to work autonomously to deliver multiple tasks of high complexity across a portfolio of products, working with team leaders to plan work across multiple teams to consistently achieve output of high quality results in a timely manner.
  • Has  a  good  understanding  of  cGMP requirements for  analytical work  in support of  clinical studies and product registration.
  • Has substantial experience of the specific challenges involved in the development, approval and commercialization of inhaled products, including dry powder inhalers.
  • Has a good understanding of material properties that impact dry powder inhaler performance in vitro and in vivo.
  • Familiar with the use of project management tools, e.g. Microsoft Project.
  • Effective verbal and written communication skills.
  • Occasional business travel as required.


At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer.

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