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 Hyderabad
Quality Control (OSD)
Stability Section in Charge : Experience : 10-11 years
Qualification : MSc/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 Oata Management * Awareness of regulatory requirement. ANDA filing & new Product filing application. Handle the FAR (Field Alert Report). Market complaint. Review & presentation of Stability Data, Tracking of raw data Chamber Management Planning for sample pullout. Batch charging. Sample storage. Sample Reconciliation, destruction & smooth functioning of Stability chamber/ Walk-in Chamber Subject Matter Expertise Awareness of routine 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 Validation of cleaning methods Handling HPLC.6C. DR and 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 to Executive
Experience : 2-8 Years
Qualification : M. Pharma/B. Pharma. Audit exposure in USFDA approved company Exposure of Material Handling / Electronic Batch Record filling and review / Good Knowledge of SAP System & Their T Codes for PP_PI / Machine Alarms handling / QMS / Deviation / Change Control / SOP / Daily Reports Preparation/ Manpower Handling
Granulation/Compression/Packing Technician :
Experience : 2-5 Years
Qualification : D.Pharma/Diploma/ ITl.
Audit exposure in USFDA approved company Working in Granulation/Compression/ Primary Bottle Packing (CVC Line) / Secondary Bottle Packing (CVC LINE) / Liquid Mfa / Liquid Filling. Good Computer knowledge / Machine Operation / Cleaning / Changeover / Alarm Handling
Eligibility : Candidate having experience to work in USFDA approved unit with good communication skills. Interested Candidate come for Walk In interview.
Walk in Interview
Date : 01st December 2024
Timing : 10:00 am to 03:30 pm
Venue : Lemon Tree Premier, Plot No. 2, Survey No. 64, HITEC City, Madhapur, Hyderabad, Telangana - 500081.
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