Head of Quality Assurance Operation
Riells i Viabrea, 西班牙 Permanent 发布于 Mar. 18, 2026 申请截止于 Apr. 08, 2026Head of Quality Assurance Operations
Location:Riells i Viabrea
Job type:Permanent
Grade level: 2
Full time
About the job
Our Team:
We are the Quality Assurance Operations team at Sanofi's site in Riells i Viabrea, dedicated to ensuring that every product we release meets the highest quality and safety standards. Our team plays a critical role in bridging production and quality, working closely with manufacturing units to guarantee compliance with Good Manufacturing Practices (GMP) and Sanofi Group regulations. We are a team driven by rigor, collaboration, and a shared commitment to patient safety.
Main responsibilities:
Compliance & Safety
- Ensure compliance with labor, quality, environmental, and safety regulations
- Apply HSE protocols including PPE usage, risk prevention, and legal certifications
Quality Management
- Define and drive Quality objectives in alignment with the Production Control Unit (PCU)
- Contribute to the site's Quality Plan
- Create, approve, and maintain general quality procedures for the PCU
- Approve manufacturing and packaging guidelines
- Manage deviations and investigations; propose and follow up on corrective and preventive actions (CAPAs)
- Participate in OOS/OOT investigations related to production
- Lead and facilitate RQN meetings when required
- Monitor change controls and follow up on actions arising from complaints
- Participate in projects, validations, and qualifications within the PCU
- Support internal and external inspections and self-inspections
Daily Operations
- Participate in daily Visual Management meetings with the PCU
- Coordinate daily work plans according to logistics priorities
- Monitor PCU activity and manage incidents
Product Release
- Act as Deputy Technical Director: release batches of medicinal products to market
- Review release documentation (manufacturing and packaging guidelines)
- Verify closure of deviations prior to release
- Record relevant data in LUNA system
- Ensure compliance with GMP, distribution requirements, and applicable regulations
Team Leadership
- Lead and develop the team, fostering a culture of growth and accountability
- Ensure team knowledge, training compliance, and adherence to procedures
- Participate in talent management initiatives
About you
- Experience:Background in Quality Assurance within the pharmaceutical industry, ideally in a production environment, with previous experience in team leadership or supervisory roles
- Technical skills:
- Hands-on knowledge of pharmaceutical manufacturing processes
- Familiarity with QMS (Quality Management Systems) and LIMS
- Experience with ERP systems (SAP preferred)
- Knowledge of GMP, ICH guidelines, and quality certifications (ISO 9001) is a plus
- Soft skills:
- Strong communication and stakeholder management skills
- Analytical thinking and problem-solving mindset
- Ability to make decisions under pressure
- Results-oriented with a continuous improvement approach
- Adaptable and open to change
- Education:Degree in Pharmacy or related life sciences field. A Master's in Pharmaceutical Quality, Regulatory Affairs, or similar is a plus
- Languages:Advanced English is required; Spanish is essential for this role
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Nota para los candidatos:
El centro de Riells, actualmente propiedad de Sanofi, forma parte de este acuerdo transaccional y está previsto que sea transferido a Adamed. Los candidatos contratados durante este período se incorporarán inicialmente con un contrato laboral de Sanofi y posteriormente serán transferidos a Adamed una vez se complete la transacción.
Al solicitar este puesto, sus datos personales serán procesados únicamente con el propósito de evaluar su candidatura. Sus datos personales serán gestionados conjuntamente por las dos empresas participantes, Adamed y Sanofi, ambas manejarán su información de forma segura y en pleno cumplimiento con el RGPD, y se conservarán únicamente durante el tiempo necesario para completar el proceso de selección.
null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!
最终薪酬将根据经验、技能、专业能力、工作地点等因素综合确定。员工可能有资格参与公司的员工福利计划。
查看所有职
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
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Sustainable and Green
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我们的故事
我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。
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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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勇敢追梦,奔赴美好未来
想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。
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我们的办公地点
我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。
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我们的人与文化
我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。
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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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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。