Executive

Job Openings Quality Control (Pharma experience only)

DESIGNATION - OFFICER / EXECUTIVE (MIN 2 TO 10 YEARS)

QUALIFICATION - B. PHARM / M.SC

DEPARTMENT - QC FORMULATION (FG / IN-PROCESS) (NASAL / DERMA / MDI & DPI)

JOB PROFILE -

• Analyze finished products (Nasal, Derma, MDI/DPI) using tests like Assay, RS, SCU, Spray Pattern, APSD (NGI), DDU, FPM, and physical tests. Operate and maintain instruments including HPLC/GC (Chromeleon), UV, pH meter, and Spray View. Ensure compliance with GMP, data integrity, and 21 CFR Part 11, with accurate QC documentation.

DESIGNATRION - OFFICER / EXECUTIVE (MIN 2 TO 10 YEARS)

QUALIFICATION - B. PHARM / M.SC

DEPARTMENT - QC API

JOB PROFILE-

• In-process, HT and stability testing of API products using HPLC, UV, GC, IR and Polarimeter. Laboratory documentation as per cGMP, GLP and data integrity; OOS / OOT investigation support.
  

DESIGNATRION - OFFICER / EXECUTIVE (MIN 2 TO 10 YEARS)

QUALIFICATION - B. PHARM / M.SC

DEPARTMENT - QC FORMULATION OSD (STABILITY SECTION)

JOB PROFILE -

• Perform stability testing of formulation products as per approved protocols. Conduct analysis using HPLC, UV, Dissolution, and other analytical instruments. Maintain laboratory documentation in compliance with cGMP, GLP, and Data Integrity requirements. Ensure timely completion of stability studies and reporting.

DESIGNATRION - OFFICER / EXECUTIVE (MIN 2 TO 10 YEARS)

QUALIFICATION - B. PHARM / M.SC

DEPARTMENT - QC FORMULATION OSD (FG / IN-PROCESS)

JOB PROFILE -

• Analysis of Finished Products (FG) using HPLC, GC, UV and other analytical instruments in OSD formulations. Expertise of pharmaceutical quality system. (LIMS/QAMS/SAP). Handling of OOS / OOT and Lab Deviation.

DESIGNATRION - OFFICER (MIN 3 TO 5 YEARS)

QUALIFICATION - B. PHARM / M.SC

DEPARTMENT - QA API

JOB PROFILE -

• Handle QMS & QRM activities. Perform IPQA checks and Line Clearance. Execute Process Validation and Cleaning Sampling. Review BPR, BMR & Cleaning Records. Verify CSV (Computer System Validation) activities. Ensure cGMP compliance and documentation accuracy.

NOTE -

1. USFDA & MHRA regulatory exposure is mandatory. Candidates without regulated-market exposure will not be considered.

2. 60% marks mandatory if experience is less than 5 years

3. Relieving letters all previous organization