a. Ensure all the PPE’S are available and shall be ware before start of activities b. Ensure that BMR and Approved RM material is available on shop floor for batch charging. c. Ensure that reactor cleaned before batch charging if not then perform cleaning then start batch as per SOP. d. Responsible for availability of all utility on side. e. RM and solvent quantity shall be charged as mention in the BMR and do online entry in the respective BMR and log book. f. Update the status board of equipment. g. Ensure that after batch charging empty drums and labels are discarded properly defacing the label. h. After batch charging all accessories used for batch shall be cleaned and label it and it should be kept in designated area. i. Maintain the parameter as per BMR and monitor till the end of activity. j. Inform to in charge if any maintenance related job to be done in the plant. k. Maintain good housekeeping in plant all the time in production facility. l. Ensure that entry and exit procedure is strictly followed in the powder processing area. m. Record daily temperature and Humidity and differential pressure. n. Do calibration of weighing balance as per pre-defined standard. o. Ensure cleaning of powder processing is done as per daily and weekly. p. Ensure personal hygiene maintained. q. Responsible for all equipment cleaning. Job Type: Full-time Pay: ₹148,825.01 - ₹350,000.00 per year Benefits: Provident Fund Education: Bachelor's (Preferred) Work Location: In person
a. Responsible for issuance of BPCRs/ECRs, Protocols, Seal, Formats, Registers/Logbooks/ Bound books, Controlled / Uncontrolled copy, Controlled /Display copy of SOP, Numbering of Qualification.(IQ/OQ/PQ/RQ/DQ/URS/SAT). b. Responsible for tracking, updating and handling of all master documents like BPCRs, ECRs, SOPs, reviewing & checking of filled BPCR/ECR, Specification, Document Archival activity. c. Responsible for review of Raw material, Packing material, in-process, intermediate, finish, cleaning specification & test method for master after approval. Responsible for master, issuance, tracking and retrieval of SOPs to all departments. a. Masters in Science (Chemistry) b. Minimum 0-1 year of work experience from pharma, preferably in quality assurance environment Knowledge and Experience in US FDA approval, GMP compliance. Job Type: Full-time Pay: ₹25,000.00 - ₹400,000.00 per year Benefits: Provident Fund Work Location: In person