Description: Production personnel are responsible for carrying out day-to-day production activities as per approved Batch Manufacturing Records (BMR), Standard Operating Procedures (SOPs), and cGMP guidelines. The role includes handling raw materials, operating and cleaning equipment, maintaining
Description: Production personnel are responsible for carrying out day-to-day production activities as per approved Batch Manufacturing Records (BMR), Standard Operating Procedures (SOPs), and cGMP guidelines. The role includes handling raw materials, operating and cleaning equipment, maintaining
Use Your Power for Purpose At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your work will leverage cutting-edge design and process development capabilities to accelerate and deliver best-in-class medicines to patients globally. Whether
Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether
What You Will Achieve In this role, you will: Evaluate and review commercial drug batches to ensure compliance with established specifications. Ensuring Zero Defect Technology transfer for new product transfers into site. Quality Support and review
Description: Responsible for managing the Quality Management System (QMS), including deviations, OOS/OOAL investigations, CAPA, change control, and ensuring compliance with cGMP and regulatory requirements. Handle audits (regulatory, customer, internal), drive SOP/document control, training systems, and ensure
Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether
Use Your Power for Purpose Responsible for execution and review support of Quality Assurance (Operations/ Compliance/ Investigations) activities including document review, shop-floor QA support, deviation handling, and quality systems support to ensure compliance with cGMP and
Use Your Power for Purpose Responsible for independent management, review, and approval of Quality Assurance activities. Ensures implementation of quality systems, drives regulatory compliance, leads investigations, and collaborates with cross-functional teams to maintain cGMP standards and
Job Purpose Lead statutory land acquisition and rehabilitation & resettlement (R&R) activities across project locations by managing acquisition planning, authority coordination, compensation processes, and stakeholder engagement to ensure timely land availability in compliance with legal and
Designation –Engineer – CAM Engineer Experience : 5 to 10 years Industry – Aerospace preferably Location- Sri City Role Summary · Develop CNC programs (3-, 4-, and 5-axis) for aerospace precision components using approved CAM software.
Role Overview We are hiring a BOM Validation Engineer who will be responsible for ensuring the accuracy, integrity, and consistency of Bills of Materials (BOMs) used across engineering, procurement, and manufacturing. The role requires a strong engineering
About SAN Automotive Industries SAN Automotive Industries Pvt. Ltd. is a forward-looking automotive component manufacturing company specializing in precision sheet metal stamping, metal fabrication, welded assemblies, tool and die manufacturing, and engineered metal components. Founded by
Greetings from P360.! About us : P360 is an advanced pharma software company specializing in business technology development and implementation for pharmaceutical and life sciences companies worldwide. We specialize in technology that boosts operational efficiency across
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Job Responsibilities Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Works to ensure that
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable
Principal Technology Engineer, Power Electronics in Photovoltaic (PV) Department: Technology Services Location: Remote, India Job Description We are seeking an experienced Principal Technology Engineer specializing in Power Electronics and MV/HV Electrical systems in Photovoltaic (PV) utility-scale
Greetings from P360.! About us : P360 is an advanced pharma software company specializing in business technology development and implementation for pharmaceutical and life sciences companies worldwide. We specialize in technology that boosts operational efficiency across
Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable