Jubilant Bhartia Group
About Jubilant Bhartia Group
Jubilant Bhartia Group stands as a prominent conglomerate committed to fostering innovation, sustainability, and excellence across diverse industries including pharmaceuticals, life sciences, and chemicals. With a rich legacy spanning several decades, the group leverages advanced technology and a customer-centric approach to deliver high-quality products and services worldwide.
As an inclusive and progressive organization, Jubilant Bhartia Group values diversity and promotes a collaborative work culture that encourages continuous learning and growth. The group is dedicated to creating a positive impact on society through its sustainable business practices and community engagement initiatives, positioning itself as a preferred employer and industry leader.
By joining Jubilant Bhartia Group, you contribute to a dynamic enterprise that emphasizes ethical standards, innovation-driven strategies, and employee empowerment. The organization actively supports professional development and provides opportunities for individuals to evolve in their careers while making meaningful contributions to global health and environment.
Long Description
The Position - Officer Production at Jubilant Biosys Limited
This role is based at our state-of-the-art manufacturing facility in Nanjangud, Mysore, where you will take ownership of critical production operations vital to our pharmaceutical development and API manufacturing processes.
Your primary responsibility is to ensure smooth and efficient production activities by overseeing equipment operations, managing materials, and maintaining compliance with quality and safety standards. You will actively participate in production planning and execution aligned with Batch Manufacturing Records (BMR) and Batch Packing Records (BPR), playing a key role in delivering products that meet regulatory and customer requirements.
This position offers an opportunity to work in a dynamic, regulated environment where precision, attention to detail, and adherence to cGMP guidelines are paramount. You will collaborate closely with cross-functional teams including quality assurance, maintenance, and supply chain to meet production targets and continuously improve manufacturing workflows.
Joining as an Officer in Production, you will be equipped with ongoing training and support to enhance your technical and functional expertise, contributing to both your career growth and the company’s success.
Long Description
Key Responsibilities
- Equipment Handling: Efficiently operate and maintain manufacturing equipment, ensuring cleanliness and performing regular troubleshooting to minimize downtime in process areas.
- Production Planning and Execution: Execute manufacturing and packaging processes as specified in BMR and BPR documentation, coordinating activities to achieve planned production schedules with high quality standards.
- Material Management: Monitor and manage consumption of raw materials, packaging components, and solvents on the shop floor, ensuring optimal utilization and accurate documentation.
- Safety, Health, and Environmental Compliance: Continuously monitor and maintain environmental conditions within the production area to meet safety protocols and regulatory requirements, promoting a safe workplace culture.
- Documentation and Reporting: Accurately maintain all production records including Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and Batch Control Records (BCR) to support traceability and audit readiness.
- Leadership and Manpower Management: Supervise and guide shop floor personnel effectively, fostering teamwork and adherence to standard operating procedures while planning daily activities to meet production targets.
Additionally, proficiency in relevant software such as cGMP certification modules, MS Office, and SAP systems is desirable to streamline operations and reporting.
Long Description
Required Skills and Functional Expertise
- Comprehensive understanding of unit operations and unit processes within pharmaceutical production environments.
- Demonstrated ability in handling detailed and complex documentation aligned with regulatory standards, including BMR, BPR, and BCR documentation.
- Solid knowledge of current Good Manufacturing Practice (cGMP) principles and their implementation on the shop floor.
- Strong critical thinking skills enabling proactive identification of potential issues and deployment of effective problem-solving approaches.
- Exceptional attention to detail ensuring product integrity, process compliance, and quality assurance at all production stages.
- Effective leadership capabilities to manage and motivate production team members, ensuring high performance and adherence to protocols.
- Competence in planning day-to-day production activities with flexibility and adaptability to meet evolving operational demands.
The successful candidate will also demonstrate a proactive approach to workplace safety and environmental standards, contributing to a culture of continuous improvement and operational excellence.
Long Description
Qualification and Experience
We seek candidates with a strong educational background and relevant industry experience to excel in this production role.
Qualification: A graduate degree in Chemical Engineering, or a Bachelor of Science in Chemistry, Physics, Mathematics, or Biochemistry is preferred. Alternatively, candidates holding a Diploma in Chemical Engineering with substantial practical experience will be considered.
Experience: A minimum of 4 years of hands-on experience within the Active Pharmaceutical Ingredient (API) manufacturing sector or equivalent process industry is essential. This should encompass exposure to batch production methodologies, equipment operation, and adherence to stringent regulatory environments.
Ideal candidates will have a proven track record within cGMP-compliant facilities, showcasing their ability to maintain high-quality standards while managing complex production schedules.
We encourage applications from individuals who are passionate about contributing to pharmaceutical manufacturing excellence, eager to develop their skills further, and committed to maintaining the highest safety and quality standards in production operations.
