Alternance - Apprenti(e) Assurance Qualité

TN France; Rueil-Malmaison; Sur place; EUR 50 000 - 90 000; Plein temps

Résumé du poste

An innovative company is seeking a Quality Senior Manager to oversee Quality System and Quality Operations at a pharmaceutical site. This role involves ensuring compliance with regulations and Good Practices, managing inspections, and supporting various quality-related activities. The position offers a unique opportunity to contribute to life-changing work in a collaborative environment, where your insights and expertise will help transform patient lives through science. Join a diverse team that values accountability, innovation, and integrity, and take your career to new heights.

Qualifications

• Experience in Quality System and Quality Operations.
• Ability to manage compliance with regulations and Good Practices.

Responsabilités

• Support Quality Assurance System and manage inspections.
• Ensure compliance with French and international regulations.

Connaissances

Regulatory Affairs

Microsoft Office

Attention to Detail

Teamwork

Multidisciplinary Collaboration

Positive Mindset

Idea Proposal

Description du poste

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Client:

Bristol Myers Squibb

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

831084f8dfef

Job Views:

2

Posted:

03.05.2025

Expiry Date:

17.06.2025

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Job Description:

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Responsible for activities related to Quality System and Quality Operations for the “Exploitant” Pharmaceutical site, in compliance with the Public Health Code, the French and international regulations, Good Practices and applicable Bristol Myers Squibb requirements as a Quality Senior Manager.

Support the Chief Pharmaceutical Officer (Responsible Pharmacist) and the Director of Quality and Pharmaceutical Affairs/Associate Director of Quality and Pharmaceutical Affairs for all Quality and pharmaceutical activities related to the Exploitant.

Support the Associate Director of Quality and Pharmaceutical Affairs for BMS France Business projects as needed.

As needed, support for Quality Assurance System :

• Documentation Quality System Management.
• Inspections, self-inspections, external audits and related action plans (CAPA) and improvements in the framework of “Exploitant process” to ensure compliance with French and international regulations, Good Practices and Bristol Myers Squibb requirements.
• Deviation / CAPA / Improvement initiatives
• Management of GXP Suppliers / Suppliers and Exploitant subcontractors.
• Change Control
• Promotional activities related to HAS Referentiel
• Business Continuity Plans
• Monitoring of new regulations and regulatory surveillance
• BMS France Business projects

Skills:

• Additional training in Regulatory Affairs
• Proficiency in Microsoft Office
• Great attention to detail
• Ability to work in a team and willingness to integrate into a group that relies on the commitment and responsibility of each individual
• Ability to work in multidisciplinary and international teams
• Positive and constructive mindset
• Strong ability to propose ideas

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and perspectives in an inclusive culture, promoting diversity in clinical trials, with shared values of passion, innovation, urgency, accountability, inclusion, and integrity that bring out the best in each of us.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based, and remote-by-design jobs. The occupancy type assigned depends on your role’s nature and responsibilities:

Site-essential roles require 100% onsite presence. Site-by-design roles may be eligible for a hybrid model with at least 50% onsite. Field-based and remote roles require ability to travel to visit customers, patients, or partners and attend meetings as directed.

BMS is committed to ensuring accessibility for people with disabilities through transparent recruitment, accommodations, and ongoing support. Applicants can request accommodations prior to accepting a job offer. For inquiries, contact . Visit to review our Equal Employment Opportunity statement.

BMS recommends full vaccination against Covid-19 and staying updated with boosters for employee and community safety.

We consider qualified applicants with arrest and conviction records, in accordance with local laws.

All data processed in connection with applications will be handled according to applicable privacy policies and regulations.