Maintain information flow at the interfaces to internal parties like packaging materials management, transport management, quality department, procurement, serialization and AW. Manage the end to end execution cycle of a Purchase Order.
Monitoring of analytical functions and ensuring real-time analytical support to the cross-function team to achieve the timeline of different projects. Analytical method validation of drug substance and different dosage forms.
To prepare change control proposal and to initiate change control in SAP. To prepare the SOP as per approved change control and assign the trainings to concern persons as per TNI in Aspire LMS system. To initiate the incident/deviation/CAPA in SAP related to warehouse.
Responsible for all commercial responsibilities sales targets & negotiation activities with non-clinical stakeholders. Shape & Create business strategies in line with local and regional strategies to grow Ethicon business in a given territory, with compliance and respecting profitability objectives.
B.Pharmacy, M.Pharmacy; ROW Market. Collaborate with Cross-Functional teams. Market Analysis. Conduct Market Research to understand industry Trends. Excellent Communication & Problem-solving skills. Data Management.
Established during the Swadeshi Movement of India, Biological E. Limited (BE) started during a time when the nation sought access to critical healthcare products. Founded and led by Dr. DVK Raju, Biological E. Limited commenced its operations in 1953 as a biological products company manufacturing liver extracts and anti-coagulants. With an objective of transitioning from treating diseases to preventing them, Biological E.
Candidates with hands on experience with Stability, finished products analysis of formulation products will be given preference. Handling of batch manufacturing and filling activity with regulatory exposure 3 Piece, BFS eye drops and Injectable in Sterile area.
To ensure timely completion of analysis and data completion for the same. To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems. M.Sc / BPharm or any relevant degree
Hands on experience of CIP, SIP skid, Vessel Operations, Compounding, filtration and autoclave, filter integrity machine.
Exposure to Isolators, Lyophilizer, single use systems.