\\nDescription Overview

As a major player in consumer health and cosmetics, Perrigo is an American pharmaceutical company committed to supporting the health and well-being of consumers through a unique portfolio of market-leading brands.

We\\xe2\\x80\\x99re currently recruiting for our recently acquired entity HRA Pharma Rare Diseases dedicated to bringing the best care and services to people living with rare diseases and is committed to supporting healthcare professionals all over the world.

We have over 15 years\\xe2\\x80\\x99 experience in rare and ultra-rare diseases with a portfolio of medicines that address Cushing\\xe2\\x80\\x99s syndrome and Adrenal Cortical Carcinoma.

We are passionate about improving the lives of people affected by these conditions. We recognize that people living with rare diseases often have severe and potentially life-threatening disabilities that impact not only their quality of life, but also the lives of those who care for them. Delays in diagnosis, together with the lack of effective treatments are just some of the challenges faced by people living with a rare disease.

We\\xe2\\x80\\x99re currently recruiting within our Global Scientific Affairs Team as Quality Manager/Officer.

In this role you will ensure that all pharmaceutical operations of the laboratory are done in compliance with applicable regulations and manage the quality and regulatory compliance of all pharmaceutical operations likely to affect the quality of marketed products and experimental drugs, such as by partners monitoring, pharmaceutical batches follow-up, handling of product defects (including pharmaceutical complaints).

Scope of the Role

Reporting to the Senior Quality Manager, your responsibilities will be:

Monitoring of the partners (manufacturers / distributors / carriers)

• Participate in writing of quality contracts, especially with manufacturers and distribution partners
• Implement a subcontracting control system and propose any improvement
• Contribute to the annual product quality review

Batch follow-up in partnership with manufacturers and distributors

• Manage the quality of products batches in liaison with the manufacturer (PQR, on-going stabilities, monthly defect product reviews)
• Validate documents relating to products quality in liaison with subcontractors (specifications, packaging instructions, ...)

Products defect management

• Ensure that the products defect management system is suitable, known to all and applied
• Work closely with the laboratory on the reporting information process
• Inform your manager in case of abnormal trends and a Qualified Person in case of critical quality issue

Batch recall

• Ensure the consistency and updating of the Laboratory \"product flows\"
• Support to the coordination of a batch recall, if necessary

Experience Required

PharmD, you have at least 3-5 years of experience providing quality support to GMP manufacturing operations and have a strong knowledge of pharmaceutical regulations, particularly of GMP& GDP.

Essential skills:

• Good level of autonomy
• Critical Thinking and Problem-Solving skills
• Good attention to detail
• An enthusiastic self-starter and team player with a positive and flexible approach to work
• Effective verbal and written communication skills
• Fluency in both French & English languages

We are a highly focused and agile company, committed to rare and ultra-rare diseases. By leveraging our strengths, we aim to become a company with truly sustainable growth and, ultimately, one of the most valued companies in rare disease field worldwide, come and join us!

Permanent position with a hybrid work model based in Chatillon, next to metro line 13 & T6 tramway.

At Perrigo we are seeking a diverse applicant pool to ensure the diversity of our team reflects the end consumers we serve through our self-care mission. We are proud to be an equal opportunity employer that celebrates our team\\xe2\\x80\\x99s differences. Individuals of all ethnicities, religious creeds, sexual orientations, genders, ages, mental and physical abilities are encouraged to apply. TOGETHER, we make lives better.\\n \\n \\n \\n \\n \\n

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