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: 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
1 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
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
Organization Profile The Amara Raja Group is one of the fastest growing conglomerates in India with a revenue exceeding USD 1.2 Billion through highly engaged customers across the Globe. Through our engaged employees, empowered teams and
Location: Dharuhera, India We are seeking an Assistant Manager, Operational Quality Assurance to ensure the highest standards of quality, compliance, and product integrity across manufacturing operations. This role will be responsible for batch release activities, in-process
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
Our vision is to transform how the world uses information to enrich life for all. Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring
Job Description Compliance to the instructions given in Batch records of various products. Ensuring the compliance of the SOPs and cGMP requirements at shop floor. Ensuring no mix-ups, contamination and cross contamination of the products during
The Opportunity: . The Opportunity: The incumbent will play a key role in ensuring product quality, regulatory compliance, and operational excellence by driving Quality Management System (QMS) and In-Process Quality Assurance (IPQA) activities across manufacturing operations. This
Job Title: Executive - Portfolio Program Qualification: Graduate / Post Graduate in Pharmacy with 3-6 years of experience in Pharmaceutical Quality Assurance or Production Candidate having sound experience in documentation as well as execution of oral
Quality Engineer / Senior Quality Engineer Location: Hyderabad Experience: 3 to 6 Years Company: Cyient DLM Limited Key Responsibilities Monitor and improve FPY (First Pass Yield) and RTY (Rolled Throughput Yield) across projects. Analyze recurring quality
Adani Group: Adani Group is a diversified organisation in India comprising 10 publicly traded companies. It has created a world class logistics and utility infrastructure portfolio that has a pan-India presence. Adani Group is headquartered in
Umendra Life Sciences is looking for an experienced Head – Quality Assurance to lead the Quality Assurance function at our pharmaceutical manufacturing facility in Bavla, Ahmedabad. This is a site-level leadership position with responsibility for the
Key Responsibilities Lead overall Quality Assurance and Quality Management System (QMS) activities in compliance with c GMP and regulatory requirements. Review and approve SOPs, BMR/BPR, specifications, validation/qualification documents, SMF, VMP and other quality documents. Manage OOS/OOT,
Quality Engineer / Senior Quality Engineer Location: Hyderabad Experience: 3 to 6 Years Company: Cyient DLM Limited Key Responsibilities Monitor and improve FPY (First Pass Yield) and RTY (Rolled Throughput Yield) across projects. Analyze recurring quality
Function/Department : QA - In Process (Drug Product Injectables) Title : Manager/Lead Job Location: Genome Valley, Shamirpet, Hyderabad Job Description: Provide line clearance and in-process QA oversight throughout manufacturing and packing operations. Ensure compliance with SOPs,
(Sr. Manager / AGM - QA) for Oral Solid Dosage (OSD) Location:- Jammu Exp:- 15-20 yrs Qualification:- B. Pharma/MSc Chemistry CTC: 15-18 LPA This role involves driving a robust culture of quality, managing a team of
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