Biocon is a research-driven, global healthcare company with a strong matrix of capabilities along the biopharmaceutical value chain. Focusing on unmet medical needs in cancer, diabetes and inflammatory diseases, it offers novel therapies on a platform of affordable innovation.
Biocon together with group companies employs more than 2500 employees with approxmimately Rs 1,000 crore turnover and is expected to grow further during the current financial year.
Post: Project Manager
Job Description:
*Managing all project activities relating to internal as well as external (out-licensed) development; from project selection to dossier submission for generic finished dosage products (FDP).
*Coordinating meetings with internal as well as external stakeholders and circulating minutes of meeting promptly.
*Coordinating activities with contract third party vendors, manufacturers, clinical research organizations (CRO) and other related functions.
*Working closely with R&D development team to provide end-to-end solution & project support from early formulation development, method development, pre-exhibit batch, exhibit batch, clinical batch, bio-study & regulatory submission activities.
*Regularly following-up with internal & external stake holders for predefined activities ensuring the project goals are met & deliverables are delivered in time.
*Working closely with commercial, operation and business development teams to provide end-to-end solution & project support from regulatory labelling, process validation, scale up, technology transfer and other related activities.
*Serving as primary support function to other project managers in advancing the development activities including PMs from CRO, CMO, third party vendors etc.
*Coordinating activities to support procurement of all finished dosage components, active & inactive ingredients, and labelling, packaging & other related components.
B.Pharm, B.Sc, B.Tech, M.B.A, M.Pharm, M.Sc, M.Tech, PGDBA, PGDBM, PGDM can apply.
Supporting regulatory affairs in filing of all dossiers for submissions & supplement / deficiency activities for regulated markets. Providing regular updates to senior management team as well as updating monthly reporting or other tracking database.
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Candidate Profile:
With a Graduate degree in Science/Technology and an MBA in project management from a Tier I institute, you have 5 to 10 years of relevant experience, specifically for pharmaceutical development in the regulated markets. You have prior experience managing different dosage forms and have handled formulation dosage products. You have displayed high levels of persistance and have a go-getter attitude with the ability to function exceptionally well in a high-pressure environment.
Skills: Good exposure on Pharma Projects (especially Formulation dosage products for regulated markets) with prior exposure to Intellectual Property Management
Additional Information:
Experience: 5-10 Years
Education: B.E, B.Pharm, B.Sc, B.Tech, M.B.A, M.Pharm, M.Sc, M.Tech, PGDBA, PGDBM, PGDM
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
End Date: 3rd Feb, 2013
Job ID: HC/JC/1281/12
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