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 accurate
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.
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 continuous quality
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
Be the First to Apply DivisionPiramal Critical Care Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by
Be the First to Apply DivisionPiramal Critical Care Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by
Use Your Power for Purpose Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting
Job Title : DATABRICKS Data Engineer (WALK-IN- 23-May Saturday) Total IT Experience : 4-10yrs Relevant Experience Required Hands-on experience in developing, maintaining, and optimizing data pipelines using Databricks. Knowledge of ETL/ELT pipelines, data ingestion, transformation, and
Position Title: Executive Department: Production Planning & Inventory Control (PPIC) Industry: Pharmaceutical API Manufacturing Experience: 5 Years (API Pharma Mandatory) Location: Visakhapatnam Key Responsibilities Production Planning Prepare monthly, weekly, and daily production plans based on sales forecasts,
Assistant Manager – Quality Control Reviewer (Pharmaceutical Formulations) Department: Quality Control (QC) Designation: Assistant Manager – QC Reviewer Experience: 8–10 Years Industry: Pharmaceutical Formulations Job Summary We are seeking an experienced and detail-oriented Quality Control Reviewer to oversee the
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 Summary We are looking for an experienced Mainframe ISV Software/Application Support Engineer to support enterprise applications and ISV software products running on IBM z/OS environments. The candidate will be responsible for L2/L3 production support, troubleshooting,
Greetings from TCS! TCS is hiring for Data Architect Experience: 8-15 years Job Location: Any Mode of Interview : Walk in Date: - 9th May26 Location of Interview: Bangalore - L‑Centre, Unit VI, No. 78, 79
Must have experience from Lyophilizers OEM (Original Equipment Manufacturers of LYO) Key Responsibilities Looking for SME for lyophilization across development, scale up, and commercial manufacturing. Experience in maintenance and qualification of CEM/Lyophiliser/HVAC/Utility/Mechanical/Water/ and RPHPLC systems in
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
Role Summary Responsible for installation, qualification and maintenance of automated equipment / instruments Role Responsibilities Key Areas Activities Equipment qualification Generation and revision of specifications (URS) Prepare engineering drawings Coordinate with CFTs for URS/DQ/IQ/OQ and PQ
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
API Production Process: Assist in the execution of Active Pharmaceutical Ingredient (API) production processes as per standard operating procedures (SOPs) and batch manufacturing records (BMRs). Operate and monitor production equipment, including reactors, centrifuges, and dryers. Ensure precise
Location : Nakkapally, Anakapali, Andhra Pradesh, India Key Responsibilities: API Production Process: Assist in the execution of Active Pharmaceutical Ingredient (API) production processes as per standard operating procedures (SOPs) and batch manufacturing records (BMRs). Operate and monitor