A pharmaceutical generics business company. HPRA Approved (April 2021) facility for veterinary generic medicines. Parent entity based in Ireland. Indian corporate office located at Gurgaon and R&D Center is at Greater Noida. Manufacturing facility based at SEZ Pithampur, Indore.
Walk In Interview at Ahmedabad
Quality Control (OSD)
Stability Section In charge :
Experience : 10-11 years.
Qualification : M.Sc./M. Pharma/B. Pharma.
Team Leading (Team management, Work allocation, preparation & Review of Stability Study Protocols, schedules, Summary Sheet, Resource management, troubleshoot in technical glitches).
Stability Data Management:- Awareness of regulatory requirement, ANDA filing & new Product filing application, Handle Field Alert Report, Market complaint, Review & presentation of Data, Tracking of data.
Chamber Management : Planning for sample pullout, Batch charging, storage & reconciliation, destruction & smooth functioning of Stability chamber/ Walk-in Chamber.
Subject Matter Expertise : Awareness of operation of Stability Study as per regulatory requirement & able to handle the regulatory audits.
QC Validation Officer to Executive :
Experience: 3-8 years.
Qualification: M.Sc./M. Pharma/B. Pharma.
Analytical methods validation, verification and methods transfer, cleaning method Validation.
Handling HPLC, GC, DR & other instruments. Preparing method validation and verification protocol and report. Reviewing analytical hard copy and electronics data.
QC Sr. Officer to Executive:
Experience: 4-8 years.
Qualification: M.Sc./M. Pharma/B. Pharma.
Working in QC analysing, Stability, In process, FP, RM sample.
Handling instruments like HPLC, GC, FTIR, UV, DR, SSA, etc, versatile in handling SAP, documentation like preparing STPs and review of analytical hard copies and electronic data.
Production (OSD)
Granulation/Compression/Packing Officer:
Experience: 2-4 years.
Qualification: M. Pharma / B. Pharma. Working in granulation & compression & Packing area.
Granulation/Compression Executive to AM :
Experience : 4-10 years.
Qualification: M. Pharma / B. Pharma. Working in granulation & compression area.
Area of Exposure : Material Handling, Electronic Batch Record filling and review, Good Knowledge of SAP System & T Codes for PP_PI, Machine Alarms handling, QMS, Deviation, Change Control, SOP, Reports Preparation, Manpower Handling and exposure in USFDAapproved company.
Technician :
Experience: 2- 5 years.
Qualification: D. Pharma / Diploma / ITI. Working in Granulation/ Compression/ Compression / Primary Bottle Packing (CVC Line) / Secondary Bottle Packing (CVC Line).
Area of Exposure: Good Computer knowledge / Machine Operation / Cleaning / Changeover/Alarm Handling.
Job Location : Pithampur Plant
Eligibility : Candidate having experience to work in USFDA approved unit with good communication skills, Interested Candidate can come for Walk In interview.
WALK IN INTERVIEW
Date : 02nd February 2025 (Sunday)
Timing : 10:00 am to 03:30 pm
Venue : Hotel NOVOTEL Ahmedabad,
Iscon Cross Roads,
Sarkhej - Gandhinagar Hwy,
next to Wide Angle Cinema,
Ahmedabad, Gujarat -380015
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