Regional Head Regulatory & Scientific Affairs (RSA), EU
Neuchatel, Switzerland
vor 13 Tg.

UNLIMIT YOURSELF Are you up for a challenge?

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We’re currently looking for :

Regional Head Regulatory & Scientific Affairs (RSA), EU With the following requirements :

  • Master’s Degree in lifehealth sciences (e.g.
  • Pharmacy, Biology, Clinical pharmacology).

  • Substantial experience in regulatory affairs for regulated therapeutic products (pharmaceuticals, medical devices, combination products, modified-risk tobacco products)
  • Proven experience leading registration strategies and direct interaction with regulatory authorities for successful new product application, approvals and post-marketing changes
  • Understanding of Quality Management Systems (QMS) and pharmacovigilance.
  • Ability to build effective teams and foster a strong collaborative culture internally and with external partners
  • Strong problem solving and organizational capabilities coupled with proven leadership skills
  • Demonstrated ability to communicate, present and influence credibly and effectively at all levels of the organization
  • Strong reputation in engaging in proactive behavior and seizing opportunities
  • Fluent in English (both written and oral) If you are also detail and customer oriented with strong business acumen, strategic, with good planning ability and providingcommunicating solutions, a team player comfortable with different externalinternal stakeholders interactions and management, you are the one we want for our RSA Team, in Philip Morris International Management S.
  • A., Research & Development (R&D) in Neuchâtel, Switzerland. As a Regional Head RSA EU you will lead respective affiliates in the region and direct all activities related to the development and implementation of regulatory strategies for NGPs to obtain registration.

    You will also provide direction to the Central Regulatory & Scientific Affairs function in order to establish registration requirements and define submission strategies, as well as work closely with Marketing and Sales to understand market prioritization for registration purposes.

    Specific responsibilities :

  • Provide regulatory oversight and support to Product Development and R&D efforts in the development across PMI’s RRP platforms by participating and leading regulatory input into cross-functional project teams
  • Engage with senior management across PMI to provide directioninput on matters related to the regulatory requirements for MRTP-
  • NCPs and ensure on-going products compliance of the RRP portfolio marketed in the region

  • Effectively manage relationships with the RSA group within PMI and relationships with regulatory authorities, where necessary, to ensure PMI regulatory applications are strategically aligned with regulators’ expectations
  • Provide leadership to the central regulatory affairs function in defining and implementing the registration activities in support of product registrations
  • Recruit, develop and maintain high caliber regulatory professionals to support individual country RA activities Why work for us?
  • Here are 3 reasons PMI is the ultimate Employer :

    1.We’re international :

    you work with clients and learn on-the-job from team members from all over the world2.We’re flexible :

    your work fits you and not the other way round, thanks to our Flexible Work Arrangement Program and3.We’re a certified top employer :

    we consider our employees to be our strongest asset, and we are developing talent throughout all levels of the organization.

    As the first multinational company in Switzerland to obtain the Equal-Salary label, for men and women, our competitive salary and compensation package is for all our employees.

    JOIN A GLOBAL MARKET LEADER If you wish to contribute to the future of our business and to the new scientific journey of the industry, please apply online.

    PMI is the world’s leading international tobacco company, with six of the world's top 15 international brands and products sold in more than 180 markets.

    In addition to the manufacture and sale of cigarettes, including the number one global cigarette brand, and other tobacco products, PMI is engaged in the development and commercialization of Reduced-Risk Products ( RRPs ).

    RRPs is the term we use to refer to products that present, are likely to present, or have the potential to present less risk of harm to smokers who switch to these products versus continued smoking.

    We have a range of RRPs in various stages of development, scientific assessment and commercialization.

    Because our RRPs do not burn tobacco, they produce far lower quantities of harmful and potentially harmful compounds than found in cigarette smoke.

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