Felix
Walk-In Drive
for Pithampur Plant (M.P.)
Eligibility: Candidate
having experience to work in USFDA approved unit with good communication
skills.
Interested Candidate come for Walk-In interview.
Quality Control (OSD)
Stability Section In charge
Experience: 10-11 years.
Qualification: M.Sc./M.Pharm/B.Pharm.
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 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.Pharm/B.Pharm.
Analytical methods validation, verification and methods transfer. Validation of cleaning methods. Handling HPLC, GC, 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.Pharm/B.Pharm.
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.
Technology Transfer (OSD/Injectable)
Officer To Executive
Experience: 3-8 Years.
Qualification: B. Pharm /M. Pharm
To prepare documents like BMRs, BPRs, protocols and reports for trial batches/scale-up batches, exhibit batches/ process validation batches. To-coordinate and execute scale up/ exhibit/ process validation batches. To prepare and review the departmental standard operating procedures.
Validation (Injectable/OSD)
Assistant Manager / Sr. Executive / Executive
Experience: 4-12 years.
Qualification: M.Pharm/B.Pharm.
Equipment Qualification, Cleaning Validation, Terminal Sterilization, Media Fill, HVAC, All Utility, Water system Qualification, CSV and SAP validation activity. Equipment Qualification, Cleaning Validation, HVAC, All Utility, Water system Qualification, CSV and SAP validation activity.
Quality Assurance (OSD)
Officer to Sr. Officer IPQA
Experience: 3-6 Years
Qualification: B. Pharma/ M. Pharma/ B.Sc./ M.Sc.
Line clearance, Sampling of In-process samples & FG sample. Review of BMR, BPR with audit trail of equipment.
Warehouse (OSD/Injectable)
Officer
Experience: 4-6 Years.
Qualification: B.sc/M.sc/B. Pharm
Receipt of raw packing material and finished goods, GRN preparation, Dispensing of raw material, SAP, WMS, QMS.
Technician
Experience: 1-3 Years
Qualification: ITI/Diploma.
Handling Finished Goods, Packing Material/ Raw Material.
Production (OSD)
Granulation/Compression/Packing Officer
Experience: 2-4 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
Primary Packing Technician
Experience: 2-5 Years
Qualification: D. Pharma/Diploma/ ITI
Audit exposure in USFDA approved company. Working in Primary Bottle Packing (CVC Line) Liquid Filling. Good Computer knowledge/Machine Operation/Cleaning/Changeover/Alarm Handling.
Date: 22 December 2024 (Sunday)
Timing: 10:00 am to 03:30 pm
Venue:
The Papaya Tree, A.B.Road Rau Circle,
Indore, MadhyaPradesh 453331
Contact No.:
9109996408,9109968966,
Email ID: [email protected]
