- Candidates with qualification B.Pharma having 10 years’ experience in Pharmaceuticals Manufacturing/Production. From WHO - GMP facilities. Approved in manufacturing of tablets, capsules, liquid, powders and external preparations. Batch manufacturing recordoverseeing the production process, drawing up a production schedule. Make sure that products are produced on time and are good quality.Candidates with qualification B.Pharma having 10 years’ experience in Pharmaceuticals Manufacturing/Production. From WHO - GMP facilities. Approved in manufacturing of tablets, capsules, liquid, powders and external preparations. Batch manufacturing recordoverseeing the production process, drawing up a production schedule. Make sure that products are produced on time and are good quality.
- Role & responsibilitiesTo approve or reject, as sees fit, starting materials, packing materials, intermediate, bulk and finished product.Preparation & approval of standard operating procedures in quality control (chemical section).Preparation & approval of specifications & method of analysis for raw materials, bulk & finish products. Documentation of finished products.Documentation & maintenance of samples for stability study. Overall documentation of qualRole & responsibilitiesTo approve or reject, as sees fit, starting materials, packing materials, intermediate, bulk and finished product.Preparation & approval of standard operating procedures in quality control (chemical section).Preparation & approval of specifications & method of analysis for raw materials, bulk & finish products. Documentation of finished products.Documentation & maintenance of samples for stability study. Overall documentation of qual
