Sandy V.
Formulation Scientist Manager @Opella
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WORK HISTORY
Formulation Scientist Manager @Opella
Compiègne, FR
Competencies & Responsibilities • Manage a formulation team of three experienced technicians: coordinate daily lab activities, set priorities, provide scientific guidance, and foster skill development. • Own the formulation workstream for assigned brands (solids, liquids…): design and execute lab programs. • Lead end to end development from lab prototypes to pilot and scale-up/tech transfer, partnering closely with Process/Industrialization to define CMAs and CPPs. • Ensure compliance & quality: develop and maintain methodical documentation (protocols, reports, batch records), align to GMP, and contribute to regulatory deliverables and change controls. • Follow up stability & performance testing • Drive cross-functional collaboration with regulatory, quality, procurement, marketing, and manufacturing internal and CDMOs to keep timelines on track. • Champion consumer-centric design, translating insights and marketing trends into product requirements (claims, sensorials, usage), aligning scientific choices with brand positioning. • Steer project delivery, identifying plan resources and timelines for my portfolio, manage risks-mitigations and report progress/milestones to governance. • Monitor external landscape and feed innovation opportunities into the pipeline.
EDUCATION
Universidad Central de Venezuela
Bachelor of Pharmacy (B.Pharm.), Industrial Technology/Technician
Schulich School of Business - York University
Master of Business Administration (MBA), Business
Université Grenoble Alpes
Ingénierie pour la Santé et le Medicament, Pharmacie Industrielle, Formulation Procédés Production
IESA
Master of Business Administration (MBA), Business Administration and Management, General
ABOUT SANDY V.
Bachelor of Science in Pharmaceutics with a Concentration in Industrial Pharmaceutical Technology, holding a Master of Business Administration degree triple-crown accredited (AACSB, EQUIS, AMBA) as well as NASPAA accredited. Also holding a Pharmaceutical Engineering Master, mention Industrial Pharmacy, Formulation, Processes and Production.Over ten years of experience in scheduling, inventory management and production process, two and a half years of experience as Regional Regulatory Affairs Specialist in Procter and Gamble where I was able to understand a broader view of the entire process involved with bringing a new product into the market, especially in the current conditions of the industry. I worked as an intern during 6 months in the department of Lean Manufacturing in Sanofi where I had the opportunity to deepen and put into practice all the acquired knowledge. Currently I am working as Project manager for new products in Delpharm - Lille. During these last 2 years, I have been able to concatenate all my experience to achieve the deployment of the projects. Abilities include focus on working under pressure and being able to meet established deadlines in order to stay in track of the planning.Career preferences include Project planning, in the area of supply chain and lean manufacturing. Interaction with a multidisciplinary team with different capacities will help to me to define my personal leadership and extend my knowledge across a wide range of interests to obtain personal and professional growth.
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