Cronus Pharma is a fast-growing, privately held veterinary pharmaceutical company located in New Jersey, dedicated to providing innovative and cost effective products to the animal health market. Our team of seasoned industry professionals have been intimately involved in the establishment, and growth of several pharmaceutical manufacturing, and distribution firms in both the human and animal health pharmaceutical industries.
Hiring FR&D -Executive's- OSD/ Injectable (Role : Formulation Scientist)
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.
• 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 ail documents related to Formulation development.
• Perform Formulation optimization with special focus on manufacturability and biopharmacoutical 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 CFT s and timely escalation to ensure document approvals on time.
• Coordinate outsourced activities at the partnor 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/Guidelinos/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.
Walk in Interview
Date & Time : 21st December 2024- Saturday ; 9 AM to 4:00 PM
Interview Location / Work Location : Cronus Pharma Specialties India Pvt Ltd,
Plot No: 1-98/5/78, Jubilee Enclave,
Madhapur, Hitech City, R R (D),
Hyderabad, Telangana - 500081
hr@Cronuspharma.com / planthr@cronuspharma.com
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