Cronus Pharma, situated in New Jersey, is a swiftly developing generic veterinary pharmaceutical company that is privately owned. Our primary goal is to offer innovative and cost-efficient products to the animal health market. The team at Cronus Pharma consists of seasoned industry professionals who have played crucial roles in the establishment and growth of various pharmaceutical manufacturing and distribution companies in both the human and animal health pharmaceutical sectors.
Greetings from Cronus Pharma!
We are conducting walk-in interview for Production Injectable (Filling Operator) & Formulation Scientist – Injectable & OSD on 21st Dec 2024
Walk-in interview details:
Date & Time: 21st December , 9.30 AM – 5.30 PM
Venue: SURVEY NO-67, 5th FLOOR, K V PLAZA, PLOT NO 78 & 79, H NO-1, 98/5/78 & 79, Jubilee Enclave Rd, Madhapur, Hyderabad, Telangana 500081.
Contact – HR (7337445197)
Open Positions
Walk In Drive For Production Injectable (Filling Operator)
Cronus Pharma invites you to a Walk-In Drive for Filling Operator roles in Production. Candidates with 2-6 years of experience and ITI/Diploma/B.Sc./B. Pharm are welcome. Explore career opportunities at Cronus Pharma! Attend our Walk-In Drive for Filling Operator positions in Production, seeking candidates with 2-6 years of experience.
We are hiring for following positions
Department: Production
Role: Filling Operator
Preferred candidate profile
- Experience required: 2 to 6 years
- Education Qualification required: ITI/ Diploma/ B.Sc. / B. Pharm
Role & responsibilities
- Setup and Operation of Equipment: Operating aseptic filling equipment such as filling machines, capping machines, and sterilization units autoclaving in accordance with standard operating procedures (SOPs) and regulatory guidelines.
- Sterilization and Sanitization: Ensuring all equipment and materials used in the filling process are properly sterilized and sanitized to maintain aseptic conditions and prevent contamination.
- Quality Assurance: Conducting in-process checks and inspections to verify product integrity, including visual inspections, measurement checks, and sampling for microbiological testing.
- Documentation and Record Keeping: Maintaining accurate records of production activities, including batch records, equipment logs, and deviation reports, to ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
- Cleaning and Maintenance: Performing routine cleaning, maintenance, and calibration of equipment to ensure optimal performance and minimize downtime.
- Safety and Compliance: Adhering to safety protocols, including wearing appropriate personal protective equipment (PPE), and following all SOPs and regulatory guidelines to maintain a safe working environment and product integrity.
- Problem Solving and Troubleshooting: Identifying and resolving equipment malfunctions, process deviations, or quality issues promptly to prevent product loss and ensure consistent product quality.
- Team Collaboration: Collaborating with other operators, supervisors, quality control personnel, and maintenance technicians to coordinate production activities, address issues, and support continuous improvement initiatives.
- Training and Development: Participating in training programs to stay updated on new equipment, processes, and regulatory requirements, and continuously improving skills and knowledge related to aseptic filling operations.
- Continuous Improvement: Contributing to process improvement initiatives by suggesting and implementing efficiency enhancements, quality improvements, and cost-saving measures to enhance overall production effectiveness.
Walk-in drive for Formulation Scientist – Injectable & OSD
Explore opportunities as a Formulation Scientist in Injectable and OSD at our walk-in drive. Candidates with M. Pharm or Ph.D. and relevant experience are encouraged to apply. Join our walk-in drive for Formulation Scientists specializing in Injectable and OSD. Ideal candidates hold an M. Pharm or Ph.D. with 3-7 years of experience.
Role: Formulation Scientist – Injectable & OSD
Preferred candidate profile
- 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.
Role & responsibilities
- 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 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 CFT s 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.
- Calibration of instrument/equipment pertaining to the department.
- 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.
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