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QC Manager

沃特福德, 爱尔兰 Permanent 发布于   Mar. 26, 2025 申请截止于   Apr. 04, 2025
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Quality Control Manager

About the job


At Sanofi, we’re committed to providing the next-gen healthcare that patients and customers need.

To lead a section of Quality Control organisation for the Waterford site.  To ensure the provision of an efficient, independent product assessment capability to verify that all products are manufactured consistently, meeting pre-defined specifications and requirements.  To provide analytical support to Manufacturing on quality related issues.  Ensure that the requirements of cGMP are met at all times.  To develop the skills, capabilities and contribution of direct reports via the performance management processes.  To develop the succession potential of all employees within the group via established talent management processes.

For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 works together at a state-of-the-art biopharmaceutical and medical device campus. Recognized through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical Center that underpin a strong commitment to health and wellbeing.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities:

  • To lead all aspects of product quality testing proactively and in accordance with cGMP.  To ensure the availability of adequate facilities, trained personnel and approved procedures for sampling, inspecting and testing starting materials, packaging materials, intermediate, bulk and finished products and monitoring environmental conditions for GMP purposes.  To be responsible for improvement in cycle times in all QC related activities.  To ensure spending is forecasted and executed in accordance with agreed budgets.
  • To ensure that the customer requirements for the QC organisation are clearly understood and agreed and are consistently and reliably met.  To provide people leadership to the team, including developing and maintaining succession plans for the QC teams.  To be an active contributor to the QO&MPT Leadership team.
  • Ability to work contribute as part of the management ream to the overall success of the site and build strong cross functional relationships.
  • To ensure effective flexible and efficient deployment of available resources, including the proactive transfer to resources between QC teams to meet varying workloads.
  • To provide a proactive and effective support for operational cGMP compliance activities and HSE initiatives in line with site systems.
  • To manage the safety performance of QC according to national legislation, site procedures and other initiatives.

About you

To excel in this role, you will need to have:

  • Significant Experience of working in a cGMP manufacturing environment.
  • Degree in Science (Chemistry, Microbiology or Pharmacy preferred).
  • Post-graduate studies as appropriate to augment primary degree is preferred.
  • Previous Lab Management or Team Leader experience is essential.
  • Operational experience of quality laboratories in a fast-moving manufacturing environment.
  • Detailed knowledge of quality management systems.
  • Effective technical knowledge of pharmaceutical plants.
  • Knowledge of requirements for cGLP, pharmacopeial methods and stability.
  • Full understanding of relevant quality and compliance regulations.
  • Able to manage projects to plan/budget.
  • Effective facilitator.
  • Good communication skills at organisation, team, and individual levels.
  • Understands KPI’s for the site.

Why choose us?

  • Bring the miracles of science to life alongside a supportive, future-focused team.
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

追寻 发展探索 菲凡

进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。

在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。

观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!

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我们的产品设计师负责帮助人们提高免疫力,物流专家负责将药物送到需要的人手中,而数据分析师则借助先进的技术改善人们的生活。在医疗健康领域,每一次进步都离不开所有人的努力。您可以自由选择自己的职业发展道路。Gig零工项目将帮助您尝试更多岗位,个性化指导将为您挖掘自己从未被发现的优势。加入我们,开启菲凡的职业发展之路。您到底可以走多远?让我们拭目以待!

体验可能性

  • 为什么选择我们?

    我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。

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  • 心怀梦想,成就一番事业

    我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。

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  • 您和我们相互依存,共同成长

    我们精心打造薪酬体系,为您的身心健康、财务健康与社交健康提供全面保障。我们有着海纳百川的包容性团队文化,无论您在哪个岗位,都能展翅高飞。

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