Bharat Biotech International Limited Walk-in Interview .Bharat Biotech International Limited Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Job Location: Ankleshwar
- Experience Required: 0 to 5 Years
- Educational Qualification: B.Tech/B.E. in Any Specialization
- Department – Process Maintenance Management/Instrumentation and Control Systems/Water Systems Management
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Job Description: Greetings from Bharat Biotech International Limited .!!
Process Maintenance Management
- Ensure the proper operation and maintenance of equipment used in the production of vaccines and injectable, including sterile systems, filling lines, and aseptic processing equipment.
- Develop and implement preventive maintenance programs that adhere to GMP standards to minimize downtime and ensure continuous production.
- Manage maintenance activities for critical production and utility systems, including HVAC, autoclaves, sterilization systems, and other aseptic equipment.
- Lead troubleshooting efforts for any process or equipment failures, ensuring prompt corrective actions are taken while complying with safety and regulatory standards.
Instrumentation and Control Systems
- Supervise the installation, calibration, and ongoing maintenance of all instrumentation and control systems in the plant, including those that monitor and control critical manufacturing parameters.
- Ensure compliance with GMP, FDA, and other regulatory standards for instrumentation used in the production of vaccines and injectables.
- Collaborate with quality assurance (QA) and validation teams to validate control systems and instrumentation for accuracy, reliability, and compliance with regulatory requirements.
- Lead troubleshooting and maintenance activities for any failures in instrumentation, ensuring immediate corrective action and minimal impact on production.
Water Systems Management
- Oversee the operation, maintenance, and monitoring of water systems, including water for injection (WFI) systems, ensuring that they meet the required pharmaceutical-grade quality and regulatory standards.
- Ensure compliance with regulatory requirements for water quality, including microbial control and endotoxin levels.
- Manage water treatment and distribution systems, coordinating routine cleaning, sanitization, and validation of these systems.
- Ensure water systems are maintained to prevent contamination and safeguard product quality.
Utility Systems Management
- Manage and maintain critical utility systems, including steam, compressed air, HVAC, and cooling systems, ensuring they meet stringent pharmaceutical manufacturing standards.
- Implement and maintain energy efficiency and sustainability practices, in line with regulatory standards and corporate sustainability goals.
- Oversee the maintenance and calibration of systems used in temperature and humidity control, which are critical for sterile production environments.
Regulatory Compliance & WHO Audits
- Lead preparation for WHO audits, FDA inspections, and other regulatory audits, ensuring all maintenance practices, systems, and equipment are fully compliant with GMP and regulatory requirements.
- Ensure the engineering and maintenance documentation, including calibration logs, preventive maintenance records, and validation documents, are accurately maintained and ready for audit.
- Collaborate with the QA team to support the resolution of audit findings and the implementation of corrective actions.
- Stay up to date on the latest regulatory changes and industry standards, ensuring the plant operates in full compliance at all times.
Validation and Qualification
- Oversee the qualification and validation of critical equipment, systems, and processes to ensure they meet all required regulatory and operational standards.
- Work closely with the validation team to develop, execute, and maintain qualification protocols for equipment, systems, and utilities.
- Ensure that all maintenance activities are aligned with the requirements of the validation master plan (VMP) and that any changes are appropriately documented and validated.
Time and Venue
14th June , 9.30 AM – 2.30 PM
CHIRON BEHRING: Plot No. 3502, GIDC Estate, Ankleshwar, Gujarat 393002
Contact – Jayjit Parmar ( 6357087017 )