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0.0 - 1.0 years
1 - 2 Lacs
ahmedabad
Work from Office
Role & responsibilities Responsible for ensuring and carrying out tasks in accordance with FDCA, CDSCO and Prohibition Excise guidelines. Responsible for preparing the ACDF application, i.e. CoPP, renewal and new manufacturing licences. Responsible for WHO GMP, Additional Product Permission, Tender Certificate, Test License Technical person approval Responsible for preparing wholesale license, loan license, audit, and inspection reports. Responsible for preparing IT application at CDSCO i.e. Test License, Form 10, From 11, Import & Export NOC Responsible to ensure and prepare renewal of licence for prohibition and excise. Also took necessary approval for Naukarnama and do return submission and other process. You will also be responsible for any other work which may be assigned to you by the management from time to time.
Posted 5 days ago
2.0 - 4.0 years
5 - 9 Lacs
ahmedabad
Work from Office
Role & responsibilities Responsible for ensuring and carrying out tasks in accordance with FDCA, CDSCO and Prohibition Excise guidelines. Responsible for preparing the ACDF application, i.e. CoPP, renewal and new manufacturing licences. Responsible for WHO GMP, Additional Product Permission, Tender Certificate, Test License Technical person approval Responsible for preparing wholesale license, loan license, audit, and inspection reports. Responsible for preparing IT application at CDSCO i.e. Test License, Form 10, From 11, Import & Export NOC Responsible to ensure and prepare renewal of licence for prohibition and excise. Also took necessary approval for Naukarnama and do return submission and other process. You will also be responsible for any other work which may be assigned to you by the management from time to time.
Posted 3 weeks ago
5.0 - 10.0 years
5 - 6 Lacs
kheda, nadiad, ahmedabad
Work from Office
B.Sc. / M.Sc. - Microbiology with 5 to 6 years of experience as Sr. Microbiologist. FDCA approved experience. Responsible for overseeing microbiological testing, ensuring product safety & adhering to regulatory standards, including those set by FDA. Required Candidate profile Ensuring adherence to FDA guidelines & other regulations for pharmaceutical manufacturing. Focused on quality control & compliance. Developing, validating & implementing new testing methods. Perks and benefits Negotiable - Depending Upon Candidate & Experience
Posted 3 weeks ago
0.0 - 5.0 years
2 - 5 Lacs
Ahmedabad
Work from Office
Role & responsibilities Knowledge and working experience in Liaising of FDCA/NARCOTICS/APP/ CGWA/ GPCB/ PESO/ POISON/FIRE NOC. Preferably in pharma industry. Preferred candidate profile Qualification : Any Graduate Experience : Minimum 1 or 2 Years / Fresher only with science graduation
Posted 1 month ago
3.0 - 5.0 years
4 - 5 Lacs
Kadi, Ahmedabad
Work from Office
Role & responsibilities Planning of day to day microbiological activities Drug substance and drug product related documentation Communication with Production & QA, Engineering for day to day update Stability study of drug substance & product BTR review Preferred candidate profile Knowledge of General Microbiological GMP/GLP awareness Current guidelines like D&C act or schedule M knowledge of FDCA requirements Job Location : Kadi Gujarat (Bus facility are available)
Posted 1 month ago
3.0 - 5.0 years
3 - 5 Lacs
Kadi, Ahmedabad
Work from Office
Role & responsibilities Planning of day to day day Microbiological activities Drug substance & drug related product labelling related documentation Communication with production & QA, Engineering for day to day update Stability study of drug substance & product BTR review Skill Requirement Knowledge of general Microbiological Knowledge of microbiological technics in pharmaceutical industry GMT/GLP awareness Current guidelines like schedule D&C act or schedule Knowledge FDCA requirement Job Location: Kadi,Gujarat ( Bus facility available from Ahmedabad,Kalol & Kadi)
Posted 2 months ago
4.0 - 6.0 years
5 - 7 Lacs
Ahmedabad
Work from Office
Responsible for ensuring and carrying out tasks in accordance with FDCA, CDSCO and Prohibition Excise guidelines. Responsible for preparing the ACDF application, i.e. CoPP, renewal and new manufacturing licences. Responsible for WHO GMP, Additional Product Permission, Tender Certificate, Test License Technical person approval Responsible for preparing wholesale license, loan license, audit, and inspection reports. Responsible for preparing IT application at CDSCO i.e. Test License, Form 10, From 11, Import & Export NOC Responsible to ensure and prepare renewal of licence for prohibition and excise. Also took necessary approval for Naukarnama and do return submission and other process. You will also be responsible for any other work which may be assigned to you by the management from time to time.
Posted 3 months ago
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