Vacancy for Quality Control Department at Mankind Pharma

Mankind Pharma, the 7^th largest Pharmaceutical Company of India, was incepted in 1995 with a meagre capital of 50 lakhs and 20 employees. Today, we are amongst the top 5 fastest growing Pharmaceutical companies of India with an employee base of more than 10000 and heading towards a turnover of INR 3000 crores.

Executive and Sr. Executive
Department : Quality Control
Openings : 03
Location : Based at Ponta Sahib Plant - HP
Qualification : Minimum science graduate from recognized university.
CTC : Would depend on experience, knowledge andcompetency.
Minimum experience :
• Should have at least 6 to 9 years of relevant experience from pharmaceutical industry (OSD, Liquid Oral and Soft gel).
• Applicant must have working experience of USFDA and EU approved Companies.
• Having strong working knowledge of liquid chromatography and Dissolution.
• Having practical in depth knowledge of Review, the calibration of all analytical instruments.
Job Description / Mandate Criteria
1. Having experience of Analytical method validation and Technology Transfer.
2. Having working experience of Empower 3 software on waters HPLC.
3. Experience on data integrity and 21 CFR part 11 compliance.
4. Working knowledge of analysis of semi-Finished Good, Finished Good, stability and Raw material.
5. Working Experience of review, the electronic data and Audit trail of all analytical instruments.

Officer and Sr. Officer
Department : Quality Control
Openings : 05
Location : Based at Ponta Sahib Plant
Qualification : Minimum science graduate from recognized university.
CTC : Would depend on experience, knowledge andcompetency.
Minimum experience :
• Should have at least 3 to 6 years of relevant experience from pharmaceutical industry (OSD, Liquid Oral and Soft gel only).
• Applicant must have working experience of USFDA and EU approved Companies.
• Having strong working knowledge of liquid chromatography and Dissolution.
Job Description / Mandate Criteria
1. Having experience of Analytical method validation and Technology Transfer.
2. Having working experience of Empower 3 software on waters HPLC.
3. Experience on data integrity and 21 CFR part 11 compliance.
4. Working knowledge of analysis of semi-Finished Good, Finished Good, stability and Raw material.
5. Having good knowledge of Audit trail