Walk-interview For Officer / Executive - Quality Control (Formulation)

Role & responsibilities

Strict Screening:

• Required Qualifications:

  Full-Time

  B.Pharm / M.Pharm / M.Sc Chemistry / M.Sc Analytical Chemistry

  only.

• Industry Type:

  Mandatorily from regulated pharmaceutical formulation manufacturing plants (

  USFDA / MHRA

  approved sites preferred).

• Shift Flexibility:

  Must be willing to work in

  all rotational shifts

  .

Positions Open for Walk-In:

1. Officer / Sr. Officer Wet Analysis (RM & PM)

• Experience Required:

  2 to 5 Years

• Core Responsibilities:

• Perform routine physical, chemical, and wet chemistry testing on incoming

  Raw Materials (APIs/Excipients)

  and

  Packaging Materials

  .
• Execute manual/automated titrations, limit tests, assays, and moisture determination (

  Karl Fischer

  ).
• Operate and calibrate laboratory instruments including

  FTIR, UV-Vis Spectrophotometers, and Autotitrators

  .
• Maintain error-free, real-time raw data logs adhering strictly to

  Good Documentation Practices (GDP)

  and

  GLP

  .

2. Officer / Executive – Stability Analysis

• Experience Required:

  2 to 7 Years

• Core Responsibilities:

• Perform physical, chemical, and instrumental analysis of stability samples at designated time intervals.
• Strong hands-on proficiency in operating, running sequences, and basic troubleshooting of

  HPLC, GC, and Dissolution apparatus

  .
• Track stability chamber pull schedules and ensure strict data integrity (

  ALCOA+ principles

  ) across software networks.
• Assist in identifying data trends and supporting laboratory investigations for

  Out of Trend (OOT)

  and

  OOS

  results.

3. Officer – Analytical Method Validation (AMV)

• Experience Required:

  2 to 4 Years

• Core Responsibilities:

• Execute high-precision physical, chemical, and instrumental analysis dedicated to

  Method Validation, Method Verification, and Method Transfer (MV/MT)

  .
• Run advanced analytical sequences on

  HPLC, GC, UV, IR, and Dissolution setups

  .
• Assist in compiling raw testing data to prepare high-quality validation protocols, transfer logs, and technical reports.
• Coordinate with internal team leads to flag parameters, discrepancies, or software anomalies observed during method validations.