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.
Walk-in Interview - Injectable / OSD Formulation
QA - (Only Experience) - Validation
Experience : 3 Years to 7 Years
Job Responsible of Executive/Sr. executive for the Validation Activities
Primary Job Responsibilities Validation :
• Responsible for validation management of OSD & injectable lines.
• Responsible for process validation and cleaning validations and respective documentation.
• Responsible for Equipment and utilities qualification and periodic validation.
• Responsible for validation management of General and cephalosporin Block
• Responsible for preparation & review of Validation protocol, sampling plan and report before its final approval.
• Responsible for preparation of SOPs and other documents related to validations & qualifications of Injectables lines.
• To Review/approve URS, DO, FAT protocols for facility/equipments/utilities and coordinate for procurement of equipment
• Coordinate with External agencies for qualifications requalification activity.
• To ensure preparations of qualification planner for each month
• To ensure qualification programme with respect to planned schedule for each month Responsible for escalation of any non-conformances and its remediations along with QMS team.
• Responsible timely closure of QMS documents related validation management and implementation respective corrective and preventive actions.
• Review of calibration certificates and Review of work orders Training of Qualification planner
Production
Experience : 5 to 8 years
Qualification : B.Pharm/M.Pharm/Bsc/Msc/B.Tech
Injectable Shift Supervisor JD :
• Supervision and Leadership: Supervising and leading a team of operators and technicians to ensure efficient and compliant production of injectable medications. This includes assigning tasks, providing guidance, and monitoring performance to achieve production targets and maintain quality standards.
• Production Planning and Coordination: Planning and coordinating production schedules to meet production goals while ensuring adherence to production timelines and regulatory requirements. This involves coordinating with other departments such as planning, quality control, and maintenance.
• Quality Assurance and Compliance: Ensuring all production activities comply with Good Manufacturing Practices (GMP),
Standard Operating Procedures (SOPs), and regulatory guidelines. Conducting regular inspections and audits to verify adherence to quality standards and addressing any deviations or non-conformances.
• Training and Development: Providing training and development opportunities for team members to enhance skills, knowledge of aseptic techniques, and understanding of regulatory requirements. Ensuring that all team members are adequately trained and competent in their roles.
• Documentation and Record Keeping: Overseeing the accurate completion of production documentation, including batch records, production reports, and logbooks. Reviewing and approving documentation to ensure completeness, accuracy, and compliance with regulatory requirements.
• Equipment and Facility Management: Monitoring and ensuring the proper operation, cleaning, and maintenance of production equipment, cleanrooms, and facilities. Coordinating with maintenance personnel for repairs, upgrades, and preventative maintenance to minimize downtime.
• Safety and Risk Management: Promoting and maintaining a culture of safety within the production team. Ensuring that safety protocols and procedures are followed, conducting safety audits, and investigating incidents or near misses to implement corrective actions and prevent recurrence.
• Continuous Improvement: Leading and supporting continuous improvement initiatives aimed at enhancing production efficiency, product quality, and cost-effectiveness. Implementing process improvements, lean manufacturing principles, and other initiatives to optimize production operations.
• Communication and Collaboration: Facilitating effective communication and collaboration between shifts, departments, and management. Participating in meetings, providing updates on production status, addressing concerns, and fostering a positive and cooperative work environment.
• Emergency Response: Acting as a point of contact and providing leadership during emergencies or unforeseen events that impact production. Implementing contingency plans and coordinating response efforts to minimize disruption and ensure continuity of operations.
Walk in Interview
Date : 6th October 2024 (Sunday)
Time : 10:00 AM to 4:00 PM
Venue : Hotel Address:- Capital O Hotel Millennium Grand Miyapur
1-72, Sriven Mall, Boliaram Rd, Jaya Prakash Narayan Nagar, Miyapur, Telangana 500049.
Send your CV : hr@Cronuspharma.com / planthr@cronuspharma.com
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