Sr. QC Officer for Pharma Industry, Dahej

Sr. QC Officer

1 Nos.
112206
Full Time
4.0 Year(s) To 10.0 Year(s)
Not Disclosed by Recruiter
Pharma / Biotech / Healthcare / Medical / R&D
Pharma/Biotech/Clinical Research
Any - Any Graduation; Any - Any Post-Graduation
Job Description:

Job Responsibilities

• Analysis of Finished products / raw materials/ in process & stability samples (Wet & Instrumental
analysis).

 

• Preparing stability trend of finished products and then sharing with all stake holders.
• Calibration of HPLCs & GC, Lab instruments as per defined procedure and schedule..
• Method validations as per applicable guidelines.
• Inventory management of reagents/columns spares etc. required for Premix analysis.
• Mobile phase preparation and their record keeping.
• Printing and preparation of record of analysis.
• Log books, in and out entries management for various activities.
• Preparation/Revision of method of analysis.
• Revision/Preparation of specifications in consultation with Purchase and other departments.
• Reporting of deviations in analysis as per LIR procedure and implementation of CAPA.
• Day to day handling of hurdles for smooth analytical work (Trouble shooting of instruments).
• To ensure good housekeeping in the working area as well as in surroundings.
• Conducting of stability studies of Premix for validation batches/Annual batches.
• To ensure compliance to all SHE guidelines and to ensure safe working.
• Maintain all standards or working standards
• Samples preparation and packing for customer evaluation

 

Company Profile

 Manufacturer of chloro amino phenol, meta amino phenol & mono chloro phenol since 2021 in Vadodara, Gujarat.

Telephonic Interview Available

  • Telephonic interview are scheduled for this job opening.
  • Interested Candidates are requested to apply and get recruiter contact number for telephonic interview.
  • Candidates can call recruiter on given contact to start telephonic interview during working hours.

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