Description: This role supports the in-process quality assurance function within a pharmaceutical manufacturing environment, contributing to the definition and specification of activities, processes, and standards required to fulfill quality requirements for manufactured materials, components, and products.
Description: This role ensures GMP and GxP compliance in dispensing, manufacturing, and packaging. Responsibilities include machine and area clearance, product sampling, in-process checks, batch record reviews, and raw material verification. The position also involves approving packaging
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the production of
cGMP and compliance review in the GMP area as per cGMP guideline. 2 Machine and area clearance. 3 Sampling of blend, intermediate stages, AQL finished product, ANSI sample, reserve sample, stability sample and In-process checks during
Description: The role is responsible for ensuring day-to-day compliance with global GMP (Good Manufacturing Practices) during manufacturing, packing, and dispensing activities at the site. The role provides on-floor quality assurance support, ensuring operations are performed as
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the production of
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the production of
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the production of
Job Description Responsible for Quality metric data collection along with critical & repeated quality issues, and status of quality initiatives/programs to be presented to senior management as part of Global Quality Corporate Steering Committee (GQCSC) meetings.
Company:Qualcomm India Private Limited Job Area:Engineering Group, Engineering Group Hardware Engineering General Summary: As a leading technology innovator, Qualcomm pushes the boundaries of whats possible to enable next-generation experiences and drives digital transformation to help create
About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals
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
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
Key Responsibilities Technical Operations & Process Excellence Lead scale-up, engineering batches, PPQ batches, process validation, and technology transfer activities. Review and approve validation protocols, reports, and batch manufacturing records. Drive process optimization, troubleshooting, revalidation, batch size
Position : Deputy Manager – QA IPQA (Sterile Injectable) Key Responsibilities Monitor and control IPQA activities in sterile injectable manufacturing, filling, and packaging areas. Ensure adherence to aseptic practices, gowning procedures, and cleanroom behavior. Review and approve batch
Job Description: QA – IPQA (In-Process Quality Assurance) Experience: 4–8 Years Qualification: B.Pharm / M.Pharm / M.Sc Key Responsibilities: Perform in-process checks during manufacturing activities. Line clearance for aseptic filling, compounding, filtration, and packing. Review BMR/BPR, logbooks,
JOB DETAILS 1. Responsible for line clearance for equipments / area 2. Responsible for in process check during manufacturing and packing 3. Responsible for review of different logs of production , packing, store 4. Responsible for
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. Youll feel
About Shalina Healthcare: Shalina Healthcare is one of the largest pharmaceutical companies in sub-Saharan Africa. For the last 40 years we have made it our mission to provide quality medicines to those who need it 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