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.
QC Validation Analyst
Experience : 4-8 years
Qualification : M.Sc / M.Pharma / B.Pharma. Analytical methods validation, verification and methods transfer. Validation of cleaning methods. Handling HPLC, GC, DR and other instruments. Preparing method validation verification protocol and report. Reviewing analytical hard copy and electronics data.
QC Sr. Officer / Executive
Experience : 4-8 Years
Qualification : M.Sc / M.Pharma / B.Pharma. Working in QC analyzing, Stability, In process, FR RM sample. Handling instruments like HPLC, GC, FTIR, UV, DR, SSA, etc, versatile in handling SAR documentation like preparing STPs and review of analytical hard copies and electronic data.
QA / QC / Microbiology - Injectable
Designation : Officer / Sr. Officer/ Executive / Sr. Executive
Experience : 4-8 years in Injectable plants.
Qualification : M.Sc. (Microbiology/ Biotechnology/ Chemistry) / M.Pharma / B.Pharma
Quality Assurance (IPQA / QMS/ Q&V)
Candidate should have experience in handling of IPQA activities. Batch record review, Audit trail review, Batch release, Process validation, cleaning validation, Media fills, Control sample management, Preparation & review of SOPs / protocols. Handling of change controls, Deviation, CAPA, Quality Risk Management, Market complaint. Qualification of Equipment's (Autoclave, Terminal Sterilizer, Washing & Depyrogenation tunnel, Filling and capping machine,etc.j&Utilities (Water system, Process gases. PSG, HVAC, etc).Review of Layouts /drawings, Validation Master planner.
Microbiology (Analyst)
Candidate should have experience in all microbiological testing and method validations (Example: Sterility, BET and MLT etc.) and must be proficient in BET testing. Candidate should have experience in GPT, Environment Monitoring, and Culture handling and have experience in Qualification of Microbiology Equipment’s/ Instruments.
Quality Control (Analyst)
Candidate should have experience in instruments qualification & calibration, handling of quality control instruments; HPLC, GC, FTIR, UV etc. Experience in chemical analysis, water analysis, RM/PM analysis, FP/ln-process and stability analysis. Method validation / verification / transfer activity& Cleaning method validation. Preparation of documents; Protocols, reports, SOP's, STP’s, etc.
Eligibility : Candidate having experience to work in USFDA approved unit with good communication skills.
Walk in Interview
Date : 29th October, 2023
Time : 10:00 am to 03:30 pm
Venue : Hotel MG Regency Baddi Himachal Pradesh 174103
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