Assoc. Director Regulatory Affairs, Marketed Products – EUCAN

Zurich, Switzerland

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• Overview


• Success


• Life at Takeda


• Opportunity


• Responsibilities


• Map

Overview

Takeda fosters a collaborative and stimulating work environment filled with opportunity and the chance to make a difference in people's lives. It is a workplace driven by integrity, one of Takeda’s long-held values that extends to both the patients we serve and our employees who develop and deliver medicines. Across our company, Takeda employees bring together diverse strengths that together create a stronger whole.

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Success

What makes a successful member of our team?

We take action and make decisions by focusing on our four priorities in this order:

• 1

  Putting the patient
  at the center



• 2

  Building trust
  with society



• 3

  Reinforcing our
  reputation



• 4

  Developing the
  business

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Life at Takeda

• Our people

  To keep delivering new value to patients, we provide growth opportunities for every employee according to their abilities and passions, and together are building a stronger organization.




• Anders Tellefsen

  Procurement Lead, Northern Europe

  “Takeda is a unique place to work as there is no ‘every-day routine’ around here – it’s very a dynamic environment where change of plans and adjustments of approach are the constants... This allows for interesting cross-function collaboration and – if you’re up for it - a high degree of influence on your daily job and workplace.”



• Yves Leurquin

  Regional Head, Europe, Vaccines

  “Takeda is a great place to work as the company invests in the continuous development of its employees offering training, coaching, mentoring and open exchanges between all levels of the organization. Also, it is fulfilling to know that, within the Vaccine Business Unit, we are developing and delivering innovative vaccines impacting the lives of millions of people around the world.”

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Opportunity

• Inclusive

  Here, you will feel welcomed, respected, and valued as a vital contributor our global team.



• Collaboration

  A strong, borderless team, we strive together towards our priorities and inspiring mission.



• Innovation

  Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.



• Values-Led

  Since 1781, the values of Takeda-ism (Integrity, Fairness, Honesty, and Perseverance) have guided everything we do—from decision-making to interacting with patients.



• People-First

  Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.



• Empowerment

  Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.

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Assoc. Director Regulatory Affairs, Marketed Products – EUCAN

Apply NowJob ID R0013506Date posted 12.17.2020Location Zurich, Switzerland

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice, Privacy Policy and Terms of Use.

Job Description

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an Associate Director, EUCAN (Europe & Canada) Regulatory Affairs Strategy Lead, Marketed Products in our Zurich office.

Here, you will be a vital contributor to our inspiring, bold mission.

OBJECTIVE:

• Collaborates to define, develop and lead regional strategies to maximize regulatory and patient access success to enable patient access to meaningful medicines in alignment with program objectives. Effectively communicates objective assessments of the likelihood of success of these regulatory strategies. Provides strategic and tactical advice and guidance to teams to achieve timely and efficient conduct of development programs, while maintaining full compliance with applicable regulatory requirements.


• Provide regulatory expertise for multiple projects and/or one highly complex project for assigned development project of responsibility.


• Mentors team members, if required, to support scope of project work.


• May be called upon to act as deputy to the regional therapeutic area lead and/ or Region regulatory head, attending internal leadership team meetings, as appropriate


• Monitors and informs on emerging trends, regulations and changes, with emphasis on those related to project areas and/ or region of responsibility enabling proactive approach and planning to future business requirements.


• For centralized products is the primary EMA contact for project(s)/products of responsibility or can delegate with oversight. Informs the business. Manages interactions with EMA and national health authorities (and HTAs jointly with value and access team in context of parallel consultation) in the Europe Union and European Economic Area for specific product(s).

ACCOUNTABILITIES:

• Leads the regulatory working team for Europe region submissions  and represents as needed at project team and ensures regional regulatory lifecycle management strategy and submission planning written and executed according to plan –


• Partner with the regional/LOC market access and LOC RA colleagues to understand market access and reimbursement topics and support opportunities to drive consolidated inputs into regional product development plans.


• For the project(s)/product(s) of responsibility, collaborates with Global and Regional colleagues for the authoring of global regulatory strategies and ensures own critical deliverables as agreed within the global regulatory strategy and planning.


• Accountable for working with other RA functions and/or vendor to ensure that regulatory submissions and approvals are achieved on schedule within region (s) of responsibility (E.g. EMA submissions for Europe). Understands importance of regulatory documents for value and access discussions and partners with access functions to support access applications as needed.


• Identifies relevant regional regulatory requirements and provides regulatory guidance, and expertise to internal team on the assigned project(s) of responsibility.  Authors and reviews regional regulatory strategies as well as executes day-to-day activities for projects or may delegates oversight.


• Leads and manages meetings and / or interactions with regulatory authorities and agency meetings.


• Regulatory reviewer in due diligence for licensing opportunities, development and /or   marketed product opportunities.


• Proactively builds/strengthens external stakeholder (Regulatory Agency, external experts, industry organizations, etc) contacts/influence to achieve Takeda strategic goals and objectives.


• Identifies regulatory requirements and trends across area(s) of responsibility, and provides regulatory guidance, and expertise to global development team and/or higher governance bodies in these areas, as requested.


• Identifies and proposes solutions to the management of resource gaps for areas of responsibility.   


• Presents to senior management as requested.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: 

• BSc degree or equivalent in science; advanced degree preferred


• Considerable pharmaceutical industry experience.  This is inclusive of thorough regulatory experience or a solid combination of regulatory and/or related experience in both development and /or post-marketing phases. 


• Ideally some experience of working oncology products


• Solid working knowledge of regulations and guidance governing drugs and biologics in all phases of development, including post-marketing, in EU (A good understanding of basic regulatory requirements in emerging markets preferred. Awareness of evidence requirements beyond the regulators (e.g. HTA bodies)


• Understands and interprets complex scientific issues across multiple projects as it relates to regulatory requirements and strategy.


• Preferred experience in managing major regulatory filing(s); and significant contributor to regulatory and/or development strategies


• Generally strong in most and acceptable in all basic skill sets such as oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability.


• Generally strong and independent skills in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.


• Generally strong in working well with others and within global teams; and acceptable at communicating with senior leadership


• Generally strong leader who is effective manager and is able to bring working teams together for common objectives. Able to mentor and develop skills of team members.


• Experience in managing personnel a plus; experience managing relationships with CROs and/or contractors also preferred.

TRAVEL REQUIREMENTS:

• Willingness to travel to various meetings, including overnight trips.


• Requires approximately up to 10-30% travel. 

WHAT TAKEDA CAN OFFER YOU

At Takeda, we are transforming the pharmaceutical industry through our R&D- driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering Our People to Shine

Discover more at takedajobs.com

*LI-TC2-EUR

Locations

Zurich, Switzerland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job ID R0013506

Apply NowEmail Me

Back to Job Navigation (Responsibilities)

Assoc. Director Regulatory Affairs, Marketed Products – EUCAN

Apply NowJob ID R0013506Date posted 12.17.2020Location Zurich, Switzerland

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that I agree with Takeda’s Privacy Notice, Privacy Policy and Terms of Use.

Job Description

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an Associate Director, EUCAN (Europe & Canada) Regulatory Affairs Strategy Lead, Marketed Products in our Zurich office.

Here, you will be a vital contributor to our inspiring, bold mission.

OBJECTIVE:

• Collaborates to define, develop and lead regional strategies to maximize regulatory and patient access success to enable patient access to meaningful medicines in alignment with program objectives. Effectively communicates objective assessments of the likelihood of success of these regulatory strategies. Provides strategic and tactical advice and guidance to teams to achieve timely and efficient conduct of development programs, while maintaining full compliance with applicable regulatory requirements.


• Provide regulatory expertise for multiple projects and/or one highly complex project for assigned development project of responsibility.


• Mentors team members, if required, to support scope of project work.


• May be called upon to act as deputy to the regional therapeutic area lead and/ or Region regulatory head, attending internal leadership team meetings, as appropriate


• Monitors and informs on emerging trends, regulations and changes, with emphasis on those related to project areas and/ or region of responsibility enabling proactive approach and planning to future business requirements.


• For centralized products is the primary EMA contact for project(s)/products of responsibility or can delegate with oversight. Informs the business. Manages interactions with EMA and national health authorities (and HTAs jointly with value and access team in context of parallel consultation) in the Europe Union and European Economic Area for specific product(s).

ACCOUNTABILITIES:

• Leads the regulatory working team for Europe region submissions  and represents as needed at project team and ensures regional regulatory lifecycle management strategy and submission planning written and executed according to plan –


• Partner with the regional/LOC market access and LOC RA colleagues to understand market access and reimbursement topics and support opportunities to drive consolidated inputs into regional product development plans.


• For the project(s)/product(s) of responsibility, collaborates with Global and Regional colleagues for the authoring of global regulatory strategies and ensures own critical deliverables as agreed within the global regulatory strategy and planning.


• Accountable for working with other RA functions and/or vendor to ensure that regulatory submissions and approvals are achieved on schedule within region (s) of responsibility (E.g. EMA submissions for Europe). Understands importance of regulatory documents for value and access discussions and partners with access functions to support access applications as needed.


• Identifies relevant regional regulatory requirements and provides regulatory guidance, and expertise to internal team on the assigned project(s) of responsibility.  Authors and reviews regional regulatory strategies as well as executes day-to-day activities for projects or may delegates oversight.


• Leads and manages meetings and / or interactions with regulatory authorities and agency meetings.


• Regulatory reviewer in due diligence for licensing opportunities, development and /or   marketed product opportunities.


• Proactively builds/strengthens external stakeholder (Regulatory Agency, external experts, industry organizations, etc) contacts/influence to achieve Takeda strategic goals and objectives.


• Identifies regulatory requirements and trends across area(s) of responsibility, and provides regulatory guidance, and expertise to global development team and/or higher governance bodies in these areas, as requested.


• Identifies and proposes solutions to the management of resource gaps for areas of responsibility.   


• Presents to senior management as requested.

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: 

• BSc degree or equivalent in science; advanced degree preferred


• Considerable pharmaceutical industry experience.  This is inclusive of thorough regulatory experience or a solid combination of regulatory and/or related experience in both development and /or post-marketing phases. 


• Ideally some experience of working oncology products


• Solid working knowledge of regulations and guidance governing drugs and biologics in all phases of development, including post-marketing, in EU (A good understanding of basic regulatory requirements in emerging markets preferred. Awareness of evidence requirements beyond the regulators (e.g. HTA bodies)


• Understands and interprets complex scientific issues across multiple projects as it relates to regulatory requirements and strategy.


• Preferred experience in managing major regulatory filing(s); and significant contributor to regulatory and/or development strategies


• Generally strong in most and acceptable in all basic skill sets such as oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability.


• Generally strong and independent skills in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.


• Generally strong in working well with others and within global teams; and acceptable at communicating with senior leadership


• Generally strong leader who is effective manager and is able to bring working teams together for common objectives. Able to mentor and develop skills of team members.


• Experience in managing personnel a plus; experience managing relationships with CROs and/or contractors also preferred.

TRAVEL REQUIREMENTS:

• Willingness to travel to various meetings, including overnight trips.


• Requires approximately up to 10-30% travel. 

WHAT TAKEDA CAN OFFER YOU

At Takeda, we are transforming the pharmaceutical industry through our R&D- driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Empowering Our People to Shine

Discover more at takedajobs.com

*LI-TC2-EUR

Locations

Zurich, Switzerland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job ID R0013506

Apply NowEmail Me

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