* Candidate shall be experienced in handling different dosage forms viz. Tablets, Capsules, Ointment, Liquid dosage forms etc.
* Must be conversant with different Regulatory guidelines and GMP requirements.
* Must be experienced in preparation, approval and execution of validation documents and GMP documents.
* Must be able to handle day to day QA activities and Quality issues that may come up during routine production work.
* Experience in handling the site at Project stage will be an added advantage.
* Must have exposure to handling different regulatory audits.
* Must be conversant will Quality Management System principles and implementation of the same.
* Previous experience of handling a team will be an added advantage.
* Handling of country audits.
* Conversant with local and international regulatory Guidelines and GMP requirements.
* Candidate should be FDA approved and experienced in liasoning with FDA.
Fact Personnel Pvt. Ltd. shall perspire to continuously research and innovate new methods... of recruitment to facilitate easier and faster recruitment and of quality personnel.
Fact Personnel Pvt. Ltd. shall always perspire to extend its horizon to entire world, and provide world class service to its clients and its candidate as well. It shall perspire to become a knowledge house for its candidate and other people involved so as to contribute to development of every single person. We consider it as our duty as not only to locate the best talent available but also to contribute to the development of individual talents as well in whatever small way we can. Read full description