About the position Job Purpose To ensure a safe, healthy, and environmentally compliant manufacturing workplace by implementing KA HSE systems & KA minimum HSE requirement, supporting production operations, meeting statutory requirements, and driving continuous improvement in
Role Summary: An Equipment Maintenance Engineer is responsible for ensuring the optimal performance, reliability, and safety of machinery and equipment used in pharmaceutical industry. This role involves planning and executing preventive and corrective maintenance, troubleshooting equipment
Description: The role is responsible for end-to-end leadership of plant operations, ensuring safe, compliant, and efficient manufacturing aligned with business objectives. The role oversees production, quality, regulatory compliance, financial performance, and people management across one or more
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Key Responsibilities Lead and manage end-to-end API production operations Plan and execute production schedules to meet quality, cost, and delivery targets Ensure compliance with cGMP, EHS, FDA/WHO guidelines Manage, mentor, and develop production teams and shift personnel Drive
Job Title: Business Development Manager - Safety Training Sales Location: Anywhere in North / West India Experience: 5+ Years Your Tasks: The Business Development Manager (BDM) for Industrial Safety Trainings will be responsible for driving sales,
Job Description – DGM – Liquid Oral Manufacturing Position: DGM – Liquid Oral Manufacturing Experience: 18–25 Years Industry: Pharmaceutical / Liquid Oral Function: Manufacturing / Production Location: South India Job Summary We are looking for an
Job Description Purpose of the Role To operate, maintain, calibrate, troubleshoot, and improve instrumentation and automation systems used in pharmaceutical manufacturing facilities, ensuring uninterrupted operations, regulatory compliance, data integrity, equipment reliability, and adherence to cGMP requirements. Key