Chantilly BioPharma Pvt Ltd., is a subsidiary of USA Pharmaceutical Drug Development company specializing in development and manufacturing of proprietary drug delivery systems, new technologies and innovative Pharmaceutical and Nutraceutical products. Chantilly BioPharma is located in state-of-the-art facility, at Hyderabad, Telangana.
Post: QC Manager
Quality control Manager:
Scope: Oversees the operation of the Chemistry Laboratory including technical leadership, functional management of personnel. Interacts with customers and management as well as with contact laboratories.
Duties/Responsibilities:
·Keep Department Head informed of any arising problems that are likely to affect the integrity of operations.
·Responsible for the transfer and validation of analytical methods developed at contract laboratories or at sister companies.
·Write detailed technical reports.
·Perform hands on analysis.
·Manage projects related to the manufacture. ·Form conclusions based on a variety of analytical data.
·Communicate conclusions to management and to Regulatory agencies.
Technical Skills Required for the Position
- Experience working in a Pharmaceutical, Biotechnology, diagnostics and/ or medical device company.
- Education requirements: Ph.D or MS Degree in related fields or Bachelor in Science with experience.
- Knowledge of utilities, equipment, methods and instrument calibration.
- Knowledge of GMP’s quality systems, and other FDA regulatory guidelines for drugs and biologics.
- Knowledge of Pharmaceutical Manufacturing operations.
- Knowledge of applicable software for Windows, i.e. Microsoft Word for Windows, Access, Excel for Windows etc.
- Ability to follow directions and work with minimal direction as a team member.
- Ability to direct others regarding work priorities and assist in ensuring their completion.
- Ability to organize and manage large quantities of documentation.
- Detail oriented, good oral and written communication skills.
- Ability to generate reports demonstrating a good command of grammar and punctuation.
- Ability to analyze data for accuracy and correctly interpret results. Draw conclusions from data to generate a sound “scientific” report.
- Ability to create necessary Spreadsheets, databases, etc. for capture of pertinent data and presentation of data supporting company operations and submissions.
- Continually stay abreast of changing regulatory requirements / standards and industry practices.
- Knowledge of utilities, equipment, methods and instrument calibration.
Candidate Profile
Ph.D or MS Degree in related fields or Bachelor in Science .2-5 years Experience in a pharmaceutical Q.C. Lab advantageous.
Additional Information:
Qualification: B.Pharm, B.Sc, M.Pharm, M.Sc, Ph.D
Experience : 2-5 years
Functional Area: QC
Location: Hyderabad
Last Date: 10th October, 2016
forward CV to
hr1.vsp@gmail.com | vsphydadmn.2@gmail.com
Posted by,
HR Admin,
Chantilly BioPharma Pvt Ltd
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