Zota Health Care Ltd. is a company domiciled in India and Incorporated under the provisions of the Companies Act, 1956. The company is engaged in the Manufacturing & Trading in Pharmaceutical Products. The company caters to both domestic and international markets since 2000.
The company possesses highly qualified and experienced professionals from the Pharmaceutical industry, who by following the most stringent standards of production assure the quality of products produced at Zota Healthcare Ltd. Highly skilled and dedicated pharmaceutical and technical professionals from floor level to marketing executives form the backbone of Zota.
Currently we are inviting the applications as per below:
Location: Zota Healthcare LTD. Special Economic Zone, Sachin
No. of position: 1
Department: Quality Control
Experience required: 2-4 year experience (Candidate with B.sc (Chemistry)/M.sc degree and with 1-2 year experience on HPLC must be compulsory)
Offered Salary: depends upon experience and as per industry standardization
Sampling of Raw Materials and Packing Materials as per respective SOP.
Testing / Analysis of Raw material, packing material, Bulk, in process and finished product chemical as well as by using UV and HPLC.
To analyses bulk, finished product of validation and regular batches by using chemical as well as UV and HPLC.
To prepare volumetric solution and to standardize it at regular intervals as per GTPs.
To prepare standard solutions, reagents and indicators and to maintain the records.
To maintain documents and record as per GDP.
Analysis & storage of the retain samples, stability samples as per schedules with proper labeling and maintain the records.
To maintain daily records of Temperature and Humidity of control Sample Room, Micro Lab and Instrument Lab.
To maintain the daily usage & cleaning log records for respective instruments.
Preparation & maintenance of working standard as per pharmacopoeias and reference standard if available.
All the activities perform as per GLP.
Visual inspection of control samples.
To calibrate instrument as per schedule and maintain records.
To report Out of Calibration to immediate supervisor and Maintenance Dept.
Cross checking /confirmation of the Rejected Raw Material and Packing Material.
To check the art work of packing material and take the sample as reference in future.
Preparation of Certificate of analysis (COA) for all RM, PM, bulk and finished product.
Maintain the inventory register for Glass wares, Chemical and Reagents.
Sampling and testing of purified water as per schedule and prepare the report.
Good verbal and written communication skills
Computer literacy and the ability to use ERP application
Scientific and numerical skills.
A logical and independent mind.
Excellent analytical skills.
Teamwork and interpersonal skills.
The below instrument Knowledge and handling experience must be compulsory