Jobs

₹ Not disclosed Mumbai

Hi,We are having an opening for Manager / Senior Manager 2 Data Science at our Mumbai location Job Summary : The role would work as an integral part of the Data & Analytics team at SUN Pharma. It invo...view more

₹ 3.25-8.25 Lacs PA Palasbari

Responsible for performing IPQA activities. . To perform process validation and cleaning validation sampling activity in shop floor. . To review new / exhibit/transfer and executed master BMRs and B...view more

₹ 3-8 Lacs PA Palasbari

1. To maintain and ensure cGMP/cGLP in the Quality Control Department. 2. To maintain documents as per GLP requirements. 3. To perform the activity as per work allotment. 4. To follow the SOP...view more

₹ Not disclosed Mumbai (All Areas)

Review and approve master documents from CMOs,such as Batch Manufacturing Records (BMR),Batch Packaging Records (BPR),specifications,validation protocols,and stability protocolsPerform batch release o...view more

₹ 4-6 Lacs PA Jammu

Preferred candidate profile Role & responsibilities . Job Responsibilities. knowledge on Quality control function like FP / RM/PM / Stability of Solid dosage forms. good knowledge on QC Instrumentatio...view more

₹ Not disclosed Mumbai

Hi,We are having an opening for Manager-Data Analytics and BA Developer at our Mumbai location. Job Summary : As a Data Visualization Analyst, a person should be passionate about Analytics and its us...view more

₹ Not disclosed Bengaluru(Hoskote)

Trending of stability data for each batch & timepointPreferred candidate profile . ....view more

₹ Not disclosed Vadodara

Role & responsibilities MS OfficeDocumentation...view more

₹ Not disclosed Ahmednagar

Education : Graduates - Microbiology/ Equivalent ( experience In Micro testing / leading )...view more

₹ Not disclosed Baska, Gujarat

Role & responsibilities . To review and maintain production schedule as per the project / priority and as per the availability of the required material & all other related resources . To review the do...view more

₹ Not disclosed Paonta Sahib

Document Integrity: To support compliance of practices to established procedures and Good Manufacturing Practice standards. . To approve the SOPs & format,batch records relating to production operati...view more

₹ Not disclosed Vadodara

Preferred candidate profile Good Technical & Communication Skills,Investigation writing,reviewing,and editing experience,candidate should have worked in USFDA work environment. ....view more