R&D Quality Senior Manager

Phiture; Lisboa; Presencial; EUR 80 000 - 100 000; Tempo integral

Resumo da oferta

A leading healthcare innovation company in Lisbon seeks an R&D Quality Senior Manager. This role focuses on ensuring global regulatory compliance by leading inspection management efforts and developing cross-functional teams for inspections. The ideal candidate has extensive experience in the pharmaceutical industry and strong organizational skills. Join an inclusive team that values diverse contributions and offers flexible work arrangements.

Serviços

Generous Total Rewards Plan

Flexible work arrangements

Opportunities for career advancement

Qualificações

• Extensive experience in inspection management within the pharmaceutical or biotechnology industry.
• Strong knowledge of global regulatory requirements and inspection processes.
• Ability to travel domestically and/or internationally for inspections.

Responsabilidades

• Develop and execute inspection management plans.
• Manage R&D inspection framework and support Regulatory Inspection Intelligence processes.
• Act as subject matter expert for inspection management.

Conhecimentos

Inspection management

Regulatory compliance knowledge

Excellent communication skills

Project management skills

Problem-solving skills

Teamwork

Formação académica

Degree Educated

Ferramentas

SharePoint

Descrição da oferta de emprego

Join our team at Amgen Capability Center Portugal, the #1 company in Best Workplaces (201–500 employees category) in 2024 by the Great Place to Work Institute. With over 400 talented individuals from more than 40 nationalities, our Lisbon center thrives at the intersection of innovation, excellence, and inspiration. This is your opportunity to explore the future of healthcare through technology and digital innovation, supporting our mission To Serve Patients.

R&D QUALITY SENIOR MANAGER

What You Will Do

Let’s do this! Let’s change the world! In this vital role the R&D Quality Senior Manager will play a crucial part in ensuring global compliance with regulatory standards by preparing and coordinating cross-functional teams for Regulatory Health Authority inspections. Responsibilities include developing and executing inspection management plans, managing and enhancing the R&D inspection framework, ensuring appropriate resourcing and time zone alignment, and supporting Regulatory Inspection Intelligence processes while contributing to operational quality initiatives. As part of the diverse, international Clinical Quality Inspection team within the Global R&D Quality organization, this individual will help strengthen the R&D Quality Inspection Management System, provide oversight of R&D processes, and lead activities related to GCP regulatory inspections.

Responsibilities

• Ensures, that because of inspection preparation activities, story boards are being developed for key processes and activities. Organizes presentations of the story boards and mock interviews in preparation of potential Sponsor inspections.
• Ensures that a cross-functional team (e.g. Quality, Clinical Operations, other functional areas, PV/GPS, GRAAS, DTI, etc.) is fully informed and prepared to support any Regulatory Health Authority inspection, worldwide.
• Acts as the subject matter expert and primary point of contact for relevant functional areas on Inspection Management to provide real-time, proactive advice and guidance.
• Raises potentially significant inspection findings/compliance risks/impact to Senior Management.
• Develops the inspection management plan for each assigned and identified Regulatory Health Authority inspection, in conjunction with the applicable Cross-Functional Team.
• Manage the R&D inspection Framework (Calendars, Distribution Lists, Inspection notifications, SharePoint Sites, Training Content, etc…).
• Liaise with R&D Quality TA Leads to develop appropriate inspection resourcing/scaling and facilities across time-zones, and align TA compliance risk identified contact (CT-RACT, specific risk management items e.g. imaging approaches).
• Support Regulatory Inspection Intelligence processes and provide input into Operational Quality Initiatives.

What We Expect Of You

We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:

• Degree Educated.
• Extensive experience in inspection management within the pharmaceutical or biotechnology industry.
• Strong knowledge of global regulatory requirements and inspection processes.
• Excellent communication and presentation skills.
• Proven ability to work effectively in a cross-functional team environment.
• Strong organizational and project management skills.
• Experience with SharePoint and other inspection management tools.
• Ability to provide proactive advice and guidance on inspection management.
• Strong problem-solving skills and the ability to raise issues effectively.
• Ability to travel domestically and/or internationally, depending on business needs, to attend inspections as needed.

What you can expect of us

• Vast opportunities to learn and move up and across our global organization.
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.
• Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.
• Flexible work arrangements.

Apply Now

Objects in your future are closer than they appear. Join us.

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Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.