Quality Management and Regulatory Compliance Officer
2 weeks ago
In the context of our growing activities, we are looking for a Regulatory Affairs Specialist to join our teams in Spain.
You will integrate a team of Regulatory Affairs professionals dedicated to Southern Europe and will have the mission to develop PLG’s local Spain Regulatory Affairs presence, taking responsibility for new regulatory activities related to Spain for several clients.
Contribute to the regulatory activities performed. Regulatory activities include pre licensing activities, new registration (sites and medicinal products) and post-approval applications.
Management of artwork generation/ labelling/creation/update of product information: provide review of packaging texts, provide format review of Summary of Product Characteristics, Patient Information Leaflets, and labelling (e.g., QRD compliance check).
Responding to internal requests for technical and/or regulatory information.
Ensuring compliance with all regulatory processes, in readiness for both internal and external audits.
Use a variety of software packages to produce correspondence and documents, maintain spreadsheets and databases, and locate information and data eg Microsoft Office Suite, Veeva Vault (or comparable EDMS), LorenZ, Trackwise, PromoMat etc
General regulatory administration duties and compliance requirements
Document and track regulatory submissions and regulatory authority approval.
Contribute to data entry in PLG tools enabling measurements of KPI, metrics for regulatory services
At least a Bachelor’s Degree in Life Sciences, ideally a Pharmacy Degree
At least 5 years of experience in RA in a Pharmaceutical Company or Service Provider
Experience in regulatory lifecycle maintenance activities for drug products (Renewals, PI updates, technical variations) in Spain and ideally EU markets.
Knowledge of ES regulation for pharmaceuticals (NCE, Biologicals and Biotech), Medical Devices, Combination products and Cosmetics
Strong computer skills, including MS Office applications, data and document management systems
Experience in project management
Fluency in Spanish and English
A proven ability to consistently deliver to tight timelines, without negatively impacting on quality or departmental budget
ProductLife Group provides world-class regulatory outsourcing and consulting services for the global life sciences industry. Headquartered in Paris, ProductLife Group has offices in countries across Europe, the Middle East, Asia, Africa, Latin America, and North America.
ProductLife Group was founded in 1994 and has since become a global industry leader, thanks to the firm’s driven and talented employees, who are always motivated by a supportive team environment as well as opportunities to learn and to grow professionally. Employees and company partners are located in offices worldwide to support clients and drive continued growth.
If you’re enthusiastic, if you welcome challenges, and if you want to grow professionally with a management team committed to your development, apply to join us.
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