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Smoking Cessation Process Science Cluster Lead

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ID:
2507041506W

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Smoking Cessation Process Science Cluster Lead

我們做什麼

Kenvue,我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎,植根於科學,是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

我們是誰

我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成,他們的職場文化中,每個聲音都很重要,每一個貢獻都受到讚賞。 我們熱衷於洞察, 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心,成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本,熱切關懷,以科學贏得信任,以勇氣解決——有絕佳的機會等著您!加入我們,塑造我們和您的未來。有關更多資訊,請按兩下 here.

Role reports to:

EMEA Tech Ops Head

位置:

Europe/Middle East/Africa, Sweden, Skane, Helsingborg

工作地點:

完全現場

你會做什麼

As part of the Kenvue EMEA Technical Operations team (EMEA Tech Ops), the Smoking Cessation Process Science Lead manages and oversees the Life Cycle Management, Technical Transfer and Process/Packaging/Cleaning Validation providing leadership, direction and technical expertise for a series of projects associated with the Nicorette Products.

The role is based in our Helsingborg Site in Sweden

 

The role includes the following activities:

  • Lead a Team of Process Scientists managing Process Science activities at internal and external manufacturing sites of the assigned cluster.

  • Provide leadership and technical oversight in strategic Technology Transfer projects, including preparation of product/process risk assessments, definition of de-risking strategies and alignment with all involved functions on the transfer plan.  

  • Lead team towards Manufacturing Process and Product Troubleshooting activities, as well as various Continuous Improvement initiatives. Drive efficient prioritization decision-making and ensure Process Science technical voice is in place in applicable site project governance forums.

  • Ensure compliance and relevance of validation strategies defined and executed by the process science team.

  • Responsible for the development of all employees within the team to meet current and future business needs: Responsible to develop technical and leadership capabilities, skills and competencies of his/her team members to make sure the Process Science Team is equipped and has the right competences across all technologies in scope (liquid, solid and gum) and is well prepared for the future product pipeline coming at the sites.

What we expect

  • Master of Science within a relevant chemistry or pharmaceutical area.

  • More than 10 years of experience in OTC and/or Pharma Manufacturing Process, Troubleshooting Management and Site Transfers Strong expertise in pharmaceutical dosage forms, such as solid dosage forms, liquids and gum (which is a plus)

  • Broad knowledge of process development and validation requirements across Process, Packaging and Cleaning.

  • Understanding of regional and global regulatory requirements related to OTC products.

  • Strong complexity and risk management skills. Ability to work and make decisions independently and on multiple projects. Problem solving.

  • Proactive strategic thinking. Strong leadership skills and Servant Leadership Attitude.

  • Experience in people leadership and development.

  • Excellent written and verbal communication, interpersonal skills and diplomacy, with ability to engage, influence and align with diverse and dispersed organizations, seniority levels and functions.

  • Flexible and persistent, with good conflict handling and negotiation skills.

  • Proficiencies in English and Microsoft Office applications are required.

What’s In It For You

  • Competitive Benefit Package
  • Paid Company Holidays, Paid Vacation, Volunteer Time, Flexible Ways of Working & More!
  • Learning & Development Opportunities
  • Employee Resource Groups 

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