SR Quality Analyst

Ferring Holding SA; São Paulo; Presencial; BRL 50.000 - 90.000; Tempo integral

Resumo da oferta

Ein innovatives Unternehmen sucht einen Qualitätsmanager, der sicherstellt, dass Produkte den höchsten Qualitätsstandards entsprechen. In dieser Rolle sind Sie verantwortlich für die Überprüfung von Fertigprodukten, die Durchführung interner Audits und die Schulung neuer Mitarbeiter. Sie arbeiten in einem dynamischen Team, das sich für die Verbesserung der Lebensqualität von Menschen weltweit einsetzt. Wenn Sie eine Leidenschaft für Qualitätssicherung haben und in einem unterstützenden Umfeld arbeiten möchten, ist dies die perfekte Gelegenheit für Sie, Ihre Karriere voranzutreiben.

Serviços

Elternzeit für alle Mitarbeiter

Umfassende Unterstützung für Familienplanung

GMP-Schulungen

Diverse Arbeitsplatzkultur

Qualificações

• Mindestens 5 Jahre Erfahrung in der Pharmaindustrie.
• Erfahrung in Qualitätssicherung und Validierung.

Responsabilidades

• Genehmigung oder Ablehnung von Fertigprodukten gemäß GMP-Standards.
• Durchführung interner Audits und Unterstützung bei Inspektionen.

Conhecimentos

Qualitätskontrolle

Kommunikationsfähigkeiten

Interpersonelle Fähigkeiten

Englisch (fließend)

Formação académica

Universitätsabschluss

Wissenschaftlicher Hintergrund

Ferramentas

LMS (Learning Management System)

Descrição da oferta de emprego

time left to apply End Date: May 14, 2025 (4 days left to apply)

job requisition id R0033793

Job Description:

At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in reproductive and women’s health, gastroenterology, and urology. Ferring + You is about working together and sharing ideas to bring science to life for patients worldwide.

Every person at Ferring works together to change lives and help people build families. To reach our full potential, we collaborate, respect, and value diverse contributions to grow as an organization and as professionals. Together, we can influence the world around us to make life and work better.

Ferring+You

You’ll be responsible for verifying that products meet defined quality standards and perform as intended throughout all phases of the production lifecycle—from development and testing to final release—ensuring safety, reliability, and compliance for end users.

Your day at Ferring

Quality Assurance (QA):

• Approve or reject finished products and review batch release documentation in accordance with product registrations and GMP standards.
• Assess temperature data during product transportation and determine the final disposition of each shipment, including evaluating excursions using product stability data.
• Conduct internal audits and self-inspections; support health authority and corporate inspections.
• Manage change control processes, action plans, and Change Control Committee (CCC) meetings; track related KPIs and follow-ups.
• Prepare and review Standard Operating Procedures (SOPs); support the document management system.
• Organize and deliver GMP training sessions; manage quality KPIs and ensure continuous improvement.
• Open and review transportation deviations; manage related KPIs and corrective actions.
• Oversee quality integration and onboarding of new employees.
• Qualify and manage customer-related activities impacting GMP compliance.

Quality Systems & Documentation:

• LMS – Key User: Support users by clarifying doubts and helping implement improvements; report system issues to global teams and monitor progress. Create user profiles and request system/module access for new employees. Draft, review, and update controlled documents according to deadlines or regulatory updates. Ensure process alignment with business purposes; approve validity extensions and obsolescence. Promote global policies and procedures locally, ensuring timely and proper implementation.
• Archive Responsible Person: Ensure proper critical document archiving procedures are followed by all employees and departments.
• Complaint Management (Local Complaint Coordinator - LCC): Manage all product quality complaints in coordination with global teams, healthcare professionals, and regulatory authorities. Ensure timely, effective complaint handling and support investigations. Provide guidance to internal staff and local partners on managing quality complaints. Monitor and report complaint-related KPIs.

Behind our innovation…There’s you

• University Degree and Scientific background
• Minimum 5 years’ experience in pharmaceuticals industry
• Experience in QA and validation
• Good communication and interpersonal skills
• Fluency in English, both written and spoken

Get inspired by our commitment to advocate for everyone’s right to build a family, no matter who you are or where you live. Our inclusive support package – “Building Families at Ferring” – provides equal policies for all employees who wish to start their family journey, subject to a minimum employment period. It includes parental leave for both birthing and non-birthing parents, extended support on family-building, and more.

Making a difference in the lives of millions means working together. Our diverse backgrounds, experiences, and perspectives help us find solutions to challenging problems, and our success depends on each team member’s contributions. Imagine your career when it’s Ferring + You.

Behind our purpose… There’s you

If our mission and your vision align, please apply!

We are committed to maintaining an inclusive and diverse workplace with equal opportunities and mutual respect for all employees, regardless of backgrounds or socioeconomic status.

Note to agencies: This search is managed by Ferring’s Talent Acquisition team. Kindly do not send spontaneous profiles.