Batch Manufacturing Jobs

Job Title: Production Shift In-charge Location: Nandesari, VadodaraPositions: 2 Education: B.Sc. / M.Sc. / Diploma in Chemical Engineering.Experience: 5-10 years of working experience in an API (Active Pharmaceutical Ingredient) and intermediate plant, with a strong understanding and practical application of GMP (Good Manufacturing Practices)Job Summary:We are seeking a highly motivated and experienced Production Shift In-charge to join our team for Pharmaceutical Company. The successful candidate will be responsible for overseeing and managing all production activities during their assigned shift, ensuring efficient operation, adherence to quality standards, and compliance with all safety and regulatory requirements. This role requires a strong leader with proven experience in pharmaceutical manufacturing, specifically in API and intermediate production.Key Responsibilities:Shift Management: Lead and supervise a team of production operators and technicians during the assigned shift. Plan and organize daily production activities to meet targets and schedules. Allocate tasks and responsibilities to team members effectively. Monitor production processes and troubleshoot any issues that arise. Ensure smooth shift transitions and effective communication with incoming/outgoing shifts.Production Operations: Oversee the manufacturing of APIs and intermediates, ensuring processes are followed according to batch production records and standard operating procedures (SOPs). Monitor raw material consumption, in-process parameters, and finished product quality. Optimize production efficiency and minimize waste. Coordinate with other departments such as Quality Control, Quality Assurance, Maintenance, and Stores to ensure seamless operations.Quality and Compliance (GMP): Ensure strict adherence to Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. Oversee the accurate and timely completion of all production documentation, including batch records, logbooks, and deviation reports. Identify and report any deviations, non-conformances, or quality incidents, and participate in investigations. Implement corrective and preventive actions (CAPA) as required. Ensure equipment and facility are maintained in a state of readiness and compliance.Safety and Environment: Promote and enforce a strong safety culture within the production area. Ensure all team members follow safety procedures and use appropriate personal protective equipment (PPE). Report any safety hazards or incidents promptly. Ensure compliance with environmental regulations.Team Development: Provide training and guidance to production operators and technicians. Foster a positive and productive working environment. Conduct performance evaluations and provide feedback to team members.Reporting: Prepare daily, weekly, and monthly production reports. Communicate production status, challenges, and achievements to management.Skills and Qualifications: Proven leadership and supervisory skills in a manufacturing environment. In-depth knowledge of API and intermediate manufacturing processes. Strong understanding and practical application of GMP, GLP, and other relevant pharmaceutical regulations. Excellent problem-solving and decision-making abilities. Strong communication (verbal and written) and interpersonal skills. Ability to work effectively in a fast-paced, dynamic environment. Proficiency in using relevant computer software for data entry and reporting. Ability to work flexible shifts, including nights, weekends, and holidays, as required.

Responsible to maintain an optimum level of manpower and over timeResponsible to ensure all operation of production adherence to cGMP complianceResponsible on manpower development (training) for quality, productivity and cost consciousnessTo train the production personnel on cGMP Trend & regulatory requirement.Monitor the work of subordinates and ensure that the necessary assistance is provided to them for their timely, adequate and accurate completion of the assigned workAccountability to ensure production planning & timely delivery of high productivity and low cost products and with compliance to cGMP.Responsible for handling CAPA, Deviation, Change Control, URS, Contingency Plan and Investigation report.Responsible for Departmental Standard Operating Procedure update and revision execute within production in DCM.Responsible to carry out production operation as per production plan and delivery on time.Other instruction by superior.

Hi,I am hiring for Production Engineer in a manufacturing company.Location-Bidadi, BangaloreJob description B.E. in Chemical with good academic records from a reputed institute. No correspondence education. Professional experience 03 to 05 years with strong background of multi product manufacturing, batch Process, material planning, knowledge of chemical process and process hazard/Hazop study from Lubrication, Oil, Grease, Chemical industry. Age 26- 30 years 1. He will be responsible for Process & Production. 2. Handle a team of 5-7 members (Workmen). 3. To Manage Production & Execute Strategic Plan related to Production. 4. Should have sound knowledge of ISO / IATF systems & ERP process 5. Should have sound knowledge in high temperature and pressure reactions. 6. A sound knowledge in chemical reactions and kinetics is desirable. 7. Co-Ordination with Purchase / Planning /Sales For all production activities 8. Should have good planning capabilities, leadership qualities, communication and inter personal skills. 9. Knowledge & experience in Production process in a batch process chemical plant would be ideal. Job Location Bidadi Bengaluru Annual salary -7-7.5 lpa