Executive
• To maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To work as Analyst and maintain the CFR 21 part -11
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
• To maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To work as Analyst and maintain the CFR 21 part -11
Maintenance Services : • To distribute the daily work to electrician/technician as per plant job request & ensure timely compliance. • To co-ordinate with mechanical and instrument person for job re
Operate boilers, steam generation systems, and associated utility equipment as per SOPs. Monitor boiler parameters such as pressure, temperature, water level, fuel consumption, and steam output. Per
Manage routine analysis of Raw Materials, Packing Materials, In-Process Samples, Intermediates, Finished APIs, and Stability Samples. Ensure timely testing and reporting of analytical results to supp
• Receipt of indigenous/imported engineering items. • Preparation of Material Receipt Note in SAP SYSTEM • In case of rejection, inform Purchase department to return back the Material to party •
Major Purpose of the Job: - • To follow cGMP as per training guidelines from the premises to their section. • To follow the respective equipment SOP’s and written procedure from BMR. • To ensure en
• To maintain and adherence of the GLP and safety procedures in laboratory. • To issuance of work data sheet / protocols from Q.A Department. • To work as Analyst and maintain the CFR 21 part -11 co
Principal task and responsibilities : • Submission of product dossiers for registration, in various countries including India as per the agreement with customers or as per the internal plan • Submis
Timely validation of all instruments in laboratory. All documents required for Regulatory compliance are maintained properly. To report any OOS/incidents/deviation discrepancy in laboratory analyst to
• To operate Effluent Treatment Plant at Dholka. • To carry out preventive maintenance of ETP equipment’s. • Treatment of inlet effluent to be done in ETP plant as per SOP. • Records to be update a
Major Purpose Of The Job:- • To follow cGMP as per training guidelines from the premises to their section. • To follow the respective equipment SOP’s and written procedure from BMR • To ensure en
Major Purpose of the Job: - • To ensure that cGMP practices shall be followed from the premises to their section. • To follow the all respective SOPs & BMR procedure in the department during operati
• Work allocation for sampling , analysis related to microbial testing based on requirement and plan for sampling and analysis of finish products, & (test procedures and SOPs, and review of anal
Production : • Supervision of production & maintenance activities of respective shift. • To ensure that every raw material used is of right quality (approved from QC, having reference Number) and qu
• To maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To work as Analyst and maintain the CFR 21 part -11
Production : • To receive crude solvents from plants and issue recovered solvents to plants. • To check the labels of raw material, packing materials and solvents before usage. • Perform column dis
• To maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To work as Analyst and maintain the CFR 21 part -11
Major Purpose of the Job: - • To follow cGMP as per training guidelines from the premises to their section. • To follow the respective equipment SOP’s and written procedure from BMR. • To ensure en
To perform the in process checks for control on production for the process / product being manufactured. To ensure Quality and cGMP compliance of the products being manufactured. Parenteral Manufact
Looking for something specific?
Browse all job categories →