Functions, Duties, Tasks:
- Elanco Manufacturing-TSMS: Responsibilities include: a) ensuring that products and manufacturing processes are in control, capable, compliant and continuously improving, b) ensuring that the TS/MS external manufacturing organization meet the Global Quality and Global Contract Manufacturing Standards. The network TSMS Sr. Director is responsible for ensuring that the right TS functional capability is in place at each of the designated internal sites.
- Elanco’s commercialization process as it relates to new products introduced to manufacturing units: Responsibilities include: a) ensuring the robust implementation and hand-over per the manufacturability review process and b) ensuring that the right technical capability (TS/MS) is in place for Elanco commercial hand-over activities within the manufacturing units. c) ensuring that robust manufacturing processes are installed and maintained throughout the product lifecycle.
- Potential Business Development and Acquisitions: Responsibilities include: a) assessing technical capabilities / gaps of potential business deals or acquisitions, b) assisting in the development of Quality/Technical and Commercial Agreements, c) reviewing and approving technical transfer plans or other technical elements to do with acquisitions.
- Partner with the wider TSMS team to grow the talent pipeline within the function
- Partner with R&D to assure appropriate allocation of support for commercialization activities as it pertains to the Pilot Plant Mission in Huningue.
Minimum Qualification (education, experience and/or training, required certifications):
- Given the anticipated agenda both drug substance and drug product experience is desired.
- Effective communication in multi-cultural settings
- Ability to influence people
- Ability to build collaborative relationships with areas inside and outside of Elanco
- Familiarity with the Elanco Global Quality Standards
- Experience in corporate TS/MS business processes
- Bachelor in a Scientific Field. Advanced Degree (Master, PhD) or equivalent experience preferred.
- Minimum of 15 years of relevant pharma/biopharma experience, including Contract Manufacturing Support / Management
- Experience in a variety of manufacturing technologies and platforms, e.g. large molecule API, small molecule API, liquids, parenteral, oral solid dose, etc.
- On-site experience as member of manufacturing site lead-team
Additional Preferences:
- Domestic and/or international travel required
- No medical sensitivities to Elanco Animal Health products
- Shift: Monday-Friday, normal flexible hours
Other Information:
- Direct reports: 3-10, 5-6 matrixed/dotted line reports
- Travel: Directors visit each of their network’s manufacturing sites and need to be available for travel to support significant investigations.
What we offer:
- Strong value-based culture
- Dynamic environment in a flat hierarchy
- Personal and organizational development
- Possibility to influence the design and strategic direction of the organization
- Flexible working / partially home office
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
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