Experience: 5 - 7 Years
Location: Delhi/NCR
Compensation: Best in the industry
Education: UG - B.Pharma - Pharmacy,B.Sc - Any Specialization, Chemistry
PG - M.Pharma - Pharmacy,M.Sc - Any Specialization, Chemistry
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Production, Maintenance, Quality
Job Description:
* Responsible mainly for preparing and reviewing protocols for
technology transfer.
* Preparing and reviewing the corporate SOP’s across
company.
* Review of preparation of Documents.
* Must be aware of global cGMP requirements, Requirements of various agencies like USFDA, EU, MCC, TGA, WHO, etc.
• Knowledge of process validation, MV and evaluation of stability data eg. stability, method validation.
* Reporting to: - VP. Quality and complaince.
Desired Candidate Profile:
* Education Qualification: - Ph.D (Chemistry / Pharma) / M.Sc. (chemistry), M Pharm/ B Pharm.
* Age: - Around 25 to 35 Yrs.
* Unerstanding of Quality systems
* Good understanding of various aspects of development and technology transfer.
* Good understanding of process validation , MV and evaluation of stability data e.g. manufacturing stability, method validation.
Company Profile:
Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.We offer stimulating work environment & a career that spells growth. In tune with our plans, we require young, aggressive, dynamic, high performing and result oriented professional.
Contact Details:
Company Name: Panacea Biotec Ltd.
Website: http://www.panacea-biotec.com//
Executive Name: Panacea Biotec Ltd
Analytical method Validation / AM BioPharma / cGMP / USFDA, EU, MCC, TGA, WHO /
Recent Comments