Vacancy for M.Pharm, B.Pharm, M.Sc in Purchase, Analytical Development at Bioplus Life Sciences

For over 75 years, Bioplus has served the pharmaceutical industry with high quality products, service, and technology. While continuing to build our global partnerships in Contract Manufacturing and EU / ANZ pharma generic pharmaceuticals, we are increasingly focused on utilizing our advanced skill set in Biotechnology. Today we are a late-stage clinical phase company with 2 programs for large global unmet needs both of which are Clinical phase 3 ready.

Post : Sr. Manager/ Manager / Sr. Research Associate / Research Associate

Sr. Manager/ Manager - Purchase
Department : Purchase
Total Experience : 14-15 Years in Pharmaceutical Purchase
Reporting to AGM - Purchase
Qualification : B.Pharm / B.Sc. / M.SC/ M.Pharma with MBA in Material Management / Supply Chain Management from premium institute
Mandatory Skills
• Good working knowledge in SAP
• Good communication Skill
Desirable Skills
• Multi-Tasking
• Go getter attitude

Job Description
• Identifying profitable suppliers and initiate business
• Analyzing quotations and bids etc., and preparation of comparative statement (quotation charts) and finalizing purchase details of orders and deliveries
• Monitoring market price trend for API, Excipients Solvents, Enzymes. Other chemicals
• Contract management and negotiation (Rate contract) and releasing purchase order as per the Company's requirement
• Sourcing the material (existing and new) from foreign countries and domestic suppliers as well as Strategic sourcing for critical commodities like API, Excipients Solvents, Enzymes. Other chemicals
• Understanding cost model and supporting cost implementation for given project
• Identifying profitable external manufacturers and suppliers, initiate business and organization partnerships with agreed terms and conditions as per company policy
• Negotiating with external manufacturers to secure advantageous terms
• Attending internal production, technical QA/QC meetings.
• Vendors visit along with QC lead for Vendor audit and supplier evaluation based on the VQ provided by the vendor, and commercial meeting
• Preparing Form-10 for import of the materials and working with CHA for clearance of import materials from customs by providing adequate data, as may be required from them
• Correspondence, coordination and dealing with suppliers carriers etc., regarding shortages, rejections and other issues reported by the QC/Production/stores Departments
• Coordinating with R&D department for any change in specification of existing material and for new material or new vendor development
• Vendor development for external manufacturers and existing/new raw material and sourcing from foreign counties and domestic, arranging samples
• Follow up for the test report if any new development raw material manufacturer samples sent to QC
• Regulatory documents follow up for API, Excipients & Solvents
• Preparing and supporting for monthly/yearly financial analysis and Procurement reports
• Maintenance of purchase records and relevant contractual documentation of CMOs preparing reports from SAP data

Sr. Research Associate / Research Associate - AR&D
Department : Analytical Development
Total Experience : 3-5 Years
Reporting to Team Leader / Department Head
Qualification : M.Pharm in Pharmaceutical Analysis from Top Colleges SCHOOL Preferably CBSE / ICSE Board students with good academic records

Job Description
• To Follow the SOPs and implementation as per GLP
• Analytical support for formulation development department in terms of analyzing in-process/finished products for drug release profiling, assay, content uniformity, blend uniformity, related substances, water content and other analysis
• Online documentation of analytical activities
• Perform day-to-day research activities to the timely completion of R&D objectives. Analytical method transfers to site Regular, API and Stability sample analysis as per stability protocol
• Regular checks during the analysis for correct method, sample, protocol usage and analysis. Ensure the availability of valid impurities & reference standards etc.
• To ensure the data/document generated in laboratory notebooks, ARDS and log books meet the quality norms as per regulatory / quality requirements
• Maintaining cleanliness and following GLP in the Lab Calibration of Analytical Equipment's and Instruments as per the Calibration Schedule