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Cronus-Walk-In’s on12th to 15th November 2024
Cronus
FR&D -Executive’s- OSD/ Injectable – 3 Years to 7 Years
⚫ Job description:
Perform formulation development activities on differentiated formulations and innovative technologies to achieve Product development. Submission of documents and coordination with liaison personnel for procuring required licenses for carrying out the development work.
Pharma
Carry out /Support Scientific literature search (Articles/patents/publications/books) and compilation of experimental data, which will facilitate decision making to achieve Product development.
• Preparation of Master formula card (MFC), scale up BMR, process evaluation plan, exhibit batch protocols, stability protocol, Dissolution profiling report, Assessment report, Tablet sub division study summary report and all documents related to Formulation development.
• Perform Formulation optimization with special focus on manufacturability and biopharmaceutical properties of drug products to achieve successful commercial drug product.
• Preparation of product development reports (PDR).
• Compilation, interpretation and review of analytical results and stability data
Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments.
• Carryout & Support Writing and Review of protocols, reports, validation plans and development report to achieve product development in compliance to quality systems Coordinate with CFTs and timely escalation to ensure document approvals on time.
• Coordinate outsourced activities at the partner site by a regular communication plan. Provide timely technical inputs and timely escalation to ensure successful task completions.
• Ensure the activities are carried out in compliance with various quality, regulatory and EHS norms.
⚫ 20. Calibration of instrument/equipment pertaining to the department.
⚫ 21. Preparation and processing of department SOPs/Guidelines/Operating instructions.
• Support and coordinate application of various regulatory licenses required for R&D, clinical, import activities. Ensure timely availability of such licenses.
• Support in Developing, maintaining, and upgrading lab facility and support facility team to maintain and run lab effectively.
• Support in Technical troubleshooting/ root cause identification/Investigation/Corrective Action and Preventive Action pertaining to product development or manufacturing activities.
Qualifications:
⚫ M. Pharm or Ph.D. in Pharmacy with minimum industrial experience of 3 to 7 years in pharmaceutical development and scale-up of products.
• Preferred area of expertise is Oral Dosage forms and Injectable formulations.
Global Product Development Experience is preferred while the core area should be the US.
• Experience of working with CROS/CDMOs would be preferred.
Interview Location / Work Location: Cronus Pharma Specialties India Pvt
Ltd, GMR Hyderabad Aviation SEZ, Mamidipally (V), Balapur (M), RR (D),
• Role: Formulation Scientist
• Industry Type: Pharmaceutical & Life Sciences Department: Research & Development
• Employment Type: Full Time, Permanent
• Role Category: Pharmaceutical & Biotechnology
Walk-In’s – 2024 – Time: 10 AM to 4:00 PM 12th November to 15th November
hr@Cronuspharma.com/planthr@cronuspharma.com
More Information HR 7337445157/7337445197