Jobs in Block D Enclave 1 - Vacancies Across Companies

Manager - Production (Injectables) Terapia - a SUN PHARMA Company

14.0 years

0 Lacs

Block D Enclave 1, Delhi, India

On-site

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Manager - Production (Injectables) Date: Jun 5, 2025 Location: Halol 1 - Operations Block D Company: Sun Pharmaceutical Industries Ltd Job Title: PMA – Manager Production (Injectables) Business Unit: SGO Grade G10 Location: Halol-1 Key Responsibilities Position Summary – This role is responsible for managing and overseeing critical aspects of the production process, ensuring adherence to quality standards and regulatory compliance. Authorize to sign as a doer/ reviewer and approval in following documents CAPA, Investigation and UPD closure Impact and Risk Assessment, Justification, FMEA Any other documents required for the execution of activities To involve, prepare, review of Investigation and to give compliance of Investigation Handling of incident, investigation, cross functional incident and investigation Handling of corrective and preventive action Handling of impact analysis and to give compliance of investigation report and UPD To undergo functional training, cGMP training or any other training identified as per schedule Any other responsibility assigned by department head after ensuring the relevant training status Travel Estimate As required Job Scope Job Requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 14+ Years Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Posted 1 week ago

Apply

Manager - Production (Injectables) SUN PHARMA

14.0 years

0 Lacs

Block D Enclave 1, Delhi, India

On-site

Job Title PMA – Manager Production (Injectables) Business Unit SGO Grade G10 Location: Halol-1 Key Responsibilities Position Summary – This role is responsible for managing and overseeing critical aspects of the production process, ensuring adherence to quality standards and regulatory compliance. Authorize to sign as a doer/ reviewer and approval in following documents CAPA, Investigation and UPD closure Impact and Risk Assessment, Justification, FMEA Any other documents required for the execution of activities To involve, prepare, review of Investigation and to give compliance of Investigation Handling of incident, investigation, cross functional incident and investigation Handling of corrective and preventive action Handling of impact analysis and to give compliance of investigation report and UPD To undergo functional training, cGMP training or any other training identified as per schedule Any other responsibility assigned by department head after ensuring the relevant training status Travel Estimate As required Job Scope Job Requirements Educational Qualification B.Pharm / M.Pharm Experience Tenure : 14+ Years Show more Show less

Posted 1 week ago

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.