Please Note: Please rename your Resume/CV to your first name + Job Title (EHS MGR) to avoid spamming or being quarantined by the system. Job Title: Manager / Assistant Manager – Environmental, Health, and Safety (EHS) Location: Tumkur, Karnataka Department: Environment Health and Safety (EHS) Reporting To: Site Head and Managing Director Experience Required: 8 to 10 years Industry Preference: API / Pharmaceutical Manufacturing Employment Type: Full-time About Natural Biogenex Private Limited (NBPL): Natural Biogenex Private Limited is a growing entity in the pharmaceutical sector committed to innovation, quality, and sustainability. At NBPL, we prioritise the safety and wellbeing of our people, the environment, and the communities we serve. As part of our commitment to responsible operations, we are seeking a dynamic and experienced EHS professional to lead and strengthen our environmental, health, and safety practices. Role Overview: The EHS Manager/Asst. Manager will be responsible for ensuring strict adherence to all applicable environmental, health, and safety regulations and standards within the facility. The role involves comprehensive risk assessments, implementation of preventive measures, emergency preparedness, and maintaining full compliance with statutory requirements. Key Responsibilities: Ensure compliance with all EHS policies , statutory and regulatory requirements (Factories Act, CPCB/SPCB, PESO, etc.) Issue and monitor Permit to Work (PTW) for various high-risk activities. Conduct and organise Safety Committee meetings , Mock Drills , Fire Drills , and Monthly Plant Safety Inspections (PSI) . Oversee the daily maintenance and operational checks of safety equipment (Fire hydrants, FAS, Sprinkler systems, Smoke Detectors, PA systems). Investigate and report unsafe acts/conditions (UA/UC) , near-misses, incidents, and accidents. Implement Corrective and Preventive Actions (CAPA) . Facilitate and participate in risk assessments including HIRA, HAZOP, QRA, JSA, and PSSR . Monitor and maintain emergency response equipment (eye wash stations, spill kits, fire extinguishers). Ensure compliance with PESO regulations , handling of Gas Bank Stations, LN2, and non-PESO solvents . Supervise testing and inspection of lifting tools, tackles, hoists, lifts, and pressure vessels. Manage and renew licences/NOCs related to Fire Safety, OSEP , and other statutory clearances. Prepare, review, and update EHS and Environment-related SOPs . Conduct On-site and Off-site Emergency Preparedness exercises , including liaison with government authorities and mutual aid teams. Oversee ETP, STP, UF, RO, MEE & ATFD operations , including troubleshooting and cost optimisation. Ensure timely submission of environmental reports to SPCB and CPCB (monthly, half-yearly, and annually). Oversee safe handling and disposal of hazardous waste , including biomedical, battery, and e-waste as per guidelines. Operate and monitor systems involving SCADA, PLC, and HMI related to waste treatment technologies. Maintain and submit reports for ESG and ESAP metrics and impact tracking. Maintain strong documentation, compliance tracking, and internal/external audit readiness. Key Competencies: Strong knowledge of environmental laws, EHS frameworks , and statutory compliance Proficient in risk identification, mitigation , and safety audits Hands-on experience with effluent treatment systems and automation tools Excellent communication, documentation , and analytical skills Leadership in emergency preparedness and crisis management Qualification: Bachelor’s/Master’s Degree in Environmental Science, Industrial Safety, Civil Engineering (M. Tech -Environment Engg) , or related field Diploma in Industrial Safety (DIS) - Preferred Certified in HIRA / HAZOP / NEBOSH / ISO 45001 – Preferred Why Join Us? 🔹 Be a part of a leading API manufacturing company with cutting-edge technology and compliance standards. 🔹 Work in a state-of-the-art Quality Control Laboratory with global regulatory standards. 🔹 Opportunity to contribute to regulatory audits and pharmaceutical quality excellence. 🔹 Competitive salary and professional development opportunities. Show more Show less

Please Note: Please rename your Resume/CV to your first name + Job Title (RAM) to avoid spamming or being quarantined by the system. Job Title: Regulatory Affairs Manager Location: Vasanthnarasapura KIADB Industrial Area, Tumkur, Karnataka Experience: 5 - 7 years experience Qualification: Bachelor’s / Master's degree in pharmacy. Industry: API (Active Pharmaceutical Ingredient) Manufacturing Compensation: - Compensation commensurate with the experience and qualifications of the candidate About Natural Biogenex Pvt. Ltd. (NBPL) Natural Biogenex Pvt. Ltd. (NBPL), a subsidiary of Natural Capsules Limited, is committed to quality, compliance, and innovation. Our state-of-the-art facility in Tumkur, Karnataka, operates under stringent Good Manufacturing Practices (GMP), ensuring the highest quality standards for pharmaceutical ingredients. To strengthen our Quality Control team, we are seeking a highly motivated and detail-oriented Executive QC who will play a crucial role in ensuring the quality, compliance, and accuracy of laboratory operations under cGMP and regulatory requirements. Position Summary: The Regulatory Affairs Manager oversees the regulatory submission processes, ensures compliance with all applicable regulations, and manages the regulatory strategy for pharmaceutical products. This role involves working closely with various departments, including R&D, Quality Assurance, and Marketing, to facilitate the development and commercialization of pharmaceutical products. Key Responsibilities: Regulatory Strategy Development: Develop and implement regulatory strategies for drug development and approval. Guide regulatory requirements and compliance to internal teams. Submission Management: Prepare and submit regulatory documents to health authorities (e.g., IND, NDA, BLA). Ensure timely and accurate submission of regulatory applications and amendments. Communication with Regulatory Authorities: Act as the primary point of contact with regulatory agencies. Manage and facilitate interactions with regulatory authorities, including meetings and responses to inquiries. Regulatory Compliance: Monitor changes in regulations and guidance to ensure compliance. Conduct audits and assessments to ensure adherence to regulatory requirements. Cross-Functional Collaboration: Work closely with R&D, Quality Assurance, and Marketing teams to ensure regulatory considerations are integrated into product development. Provide training and support to staff on regulatory processes and compliance. Project Management: Manage multiple regulatory projects simultaneously, ensuring timelines and deliverables are met. Coordinate with cross-functional teams to facilitate project milestones. Documentation and Record-Keeping: Maintain accurate records of regulatory submissions and communications. Prepare and review regulatory documentation for accuracy and completeness. Qualifications: Education: Bachelor’s / Master's degree in pharmacy, Experience: Minimum of 6-8 years of experience in regulatory affairs within the pharmaceutical industry for filing of products in various regulatory agencies. Knowledge: Strong understanding of regulatory guidelines and compliance requirements (FDA, EMA, etc.). Skills: Excellent communication, organizational, and project management skills. Ability to work collaboratively in a fast-paced environment. Why Join Us? 🔹 Be a part of a leading API manufacturing company with cutting-edge technology and compliance standards. 🔹 Work in a state-of-the-art Quality Control Laboratory with global regulatory standards. 🔹 Opportunity to contribute to regulatory audits and pharmaceutical quality excellence. 🔹 Competitive salary and professional development opportunities. Show more Show less

Please Note: Please rename your Resume/CV to your first name + Job Title (PM) to avoid spamming or being quarantined by the system. Job Title : Production Manager - API Location : Vasanthnarasapura KIADB Industrial Area, Tumkur, Karnataka Experience : 10 - 15 years experience Qualification : MSc.(Organic Chemistry)/ MTech – Chemical (Technology)/ BSc.(Chemistry) Industry : API (Active Pharmaceutical Ingredient) Manufacturing Compensation: - Compensation commensurate with the experience and qualifications of the candidate About Natural Biogenex Pvt. Ltd. (NBPL). Natural Biogenex Pvt. Ltd. (NBPL), a subsidiary of Natural Capsules Limited, is committed to quality, compliance, and innovation. Our state-of-the-art facility in Tumkur, Karnataka, operates under stringent Good Manufacturing Practices (GMP), ensuring the highest quality standards for pharmaceutical ingredients. Job Description: We are seeking an experienced Production Manager to oversee and manage API production operations. The ideal candidate will have in-depth knowledge of utility operations, shop floor management, batch planning, and execution. Responsibilities include troubleshooting production issues, ensuring the production of quality products in line with GMP standards, and maintaining compliance with international regulatory bodies such as USFDA, WHO, and ICH-Q7A. Key responsibilities include : Supervision of day-to-day shop floor operations and workforce management. Ensuring batch planning, timely execution, and adherence to production timelines. Troubleshooting production and operational issues efficiently. Ensuring compliance with quality guidelines and regulatory standards (GMP, ICH-Q7A, USFDA). Experience in unit operations, including reactors (GLR, SSR, Hastelloy Autoclave), clean room operations, jet mills, AHU, and related utilities. Handling steroidal and anticancer molecules, including operations and safety protocols. Managing documentation according to SOP and GMP guidelines. Leading customer and regulatory audits, including USFDA, TGA, and WHO Geneva. Training and developing team members to enhance departmental performance. Coordination for BOQ preparation and store management. Overseeing finished goods handling and ensuring customer requirements are met. Qualifications: Education : MSc.(Organic Chemistry)/ MTech – Chemical (Technology)/ BSc.(Chemistry) Experience : Minimum of 12 - 15 years of experience Knowledge : Strong understanding various production compliances and production strategies. Skills : Excellent communication, organizational, and project management skills. Ability to work collaboratively in a fast-paced environment. Why Join Us? 🔹 Be a part of a leading API manufacturing company with cutting-edge technology and compliance standards. 🔹 Work in a state-of-the-art Quality Control Laboratory with global regulatory standards. 🔹 Opportunity to contribute to regulatory audits and pharmaceutical quality excellence. 🔹 Competitive salary and professional development opportunities.

As a Production Manager at Natural Biogenex Pvt. Ltd. (NBPL), a subsidiary of Natural Capsules Limited, located in Vasanthnarasapura KIADB Industrial Area, Tumkur, Karnataka, you will play a crucial role in overseeing and managing API production operations. With 10-15 years of experience in the industry and a background in MSc.(Organic Chemistry)/ MTech Chemical (Technology)/ BSc.(Chemistry), you will ensure the highest quality standards for pharmaceutical ingredients in compliance with international regulatory bodies such as USFDA, WHO, and ICH-Q7A. Your responsibilities will include supervising day-to-day shop floor operations, workforce management, batch planning, and execution. Your expertise in utility operations, shop floor management, and troubleshooting production issues will be essential in maintaining compliance with GMP standards and regulatory guidelines. You will lead customer and regulatory audits, oversee finished goods handling, and ensure customer requirements are met. Key Responsibilities: - Supervision of day-to-day shop floor operations and workforce management. - Ensuring batch planning, timely execution, and adherence to production timelines. - Troubleshooting production and operational issues efficiently. - Ensuring compliance with quality guidelines and regulatory standards (GMP, ICH-Q7A, USFDA). - Experience in unit operations, including reactors, clean room operations, jet mills, AHU, and related utilities. - Managing documentation according to SOP and GMP guidelines. - Leading customer and regulatory audits, including USFDA, TGA, and WHO Geneva. - Training and developing team members to enhance departmental performance. - Coordinating for BOQ preparation and store management. - Overseeing finished goods handling and ensuring customer requirements are met. Qualifications: - Education: MSc.(Organic Chemistry)/ MTech Chemical (Technology)/ BSc.(Chemistry) - Experience: Minimum of 12 - 15 years of experience - Knowledge: Strong understanding of various production compliances and strategies. - Skills: Excellent communication, organizational, and project management skills. Ability to work collaboratively in a fast-paced environment. Join us at NBPL to be a part of a leading API manufacturing company with cutting-edge technology, global compliance standards, and the opportunity to contribute to regulatory audits and pharmaceutical quality excellence. Competitive salary and professional development opportunities await you in our state-of-the-art Quality Control Laboratory.,

As the Regulatory Affairs Manager at Natural Biogenex Pvt. Ltd. (NBPL), you will be responsible for overseeing the regulatory submission processes, ensuring compliance with all applicable regulations, and managing the regulatory strategy for pharmaceutical products. Your role will involve working closely with various departments such as R&D, Quality Assurance, and Marketing to facilitate the development and commercialization of pharmaceutical products. Your key responsibilities will include developing and implementing regulatory strategies for drug development and approval, guiding regulatory requirements and compliance to internal teams, preparing and submitting regulatory documents to health authorities, managing communication with regulatory authorities, monitoring changes in regulations to ensure compliance, working collaboratively with cross-functional teams, managing multiple regulatory projects simultaneously, and maintaining accurate records of regulatory submissions and communications. To excel in this role, you should possess a Bachelor's or Master's degree in pharmacy, along with a minimum of 12 - 15 years of experience in regulatory affairs within the pharmaceutical industry for filing products in various regulatory agencies. You should have a strong understanding of regulatory guidelines and compliance requirements (such as FDA, EMA, etc.), excellent communication, organizational, and project management skills, and the ability to work collaboratively in a fast-paced environment. By joining Natural Biogenex Pvt. Ltd., you will have the opportunity to be a part of a leading API manufacturing company with cutting-edge technology and compliance standards. You will work in a state-of-the-art Quality Control Laboratory with global regulatory standards, contribute to regulatory audits and pharmaceutical quality excellence, and benefit from competitive salary and professional development opportunities.,

As a Sr. Executive / Asst Manager (Shift Incharge) in the Production Fermentation (Upstream) department at Natural Biogenex Pvt. Ltd., you will play a crucial role in overseeing and leading shift-wise operations effectively. With 6 to 10 years of experience and a background in M.Sc. / B.Tech. / B.Sc. in Biotechnology, Microbiology, or Industrial Microbiology, you will be responsible for ensuring the smooth functioning of fermentation processes in compliance with SOPs and production schedules. Your key responsibilities will include supervising and monitoring shift activities, ensuring operational efficiency, timely escalation of issues, maintaining documentation as per GMP standards, managing shift planning and manpower allocation, promoting a culture of safety-first practices, and assisting in data analysis for process improvement. Your strong technical knowledge of fermentation processes, effective team leadership skills, and sound decision-making abilities will be essential in driving optimal plant efficiency and adherence to regulatory standards. At Natural Biogenex Pvt. Ltd., you will have the opportunity to work in a modern biotech production environment, with structured career growth plans, exposure to advanced fermentation technologies, and a professional and inclusive work culture. Joining our team will allow you to be a part of a leading API manufacturing company with cutting-edge technology, global regulatory standards, and opportunities for professional development and competitive compensation.,