Job for M.Pharm, M.Sc, B.Pharm in Quality Control as Assistant Manager at Pfizer

Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

Post: Assistant Manager - Quality Control

Walk in interview for M.Pharm, M.Sc in Quality Control, Quality Assurance at Macleods

Macleods has its presence in over 30 countries with more than 300 registrations.The export range of Macleods are manufactured in a unit that has QSM approval from WHO-Geneva, and certifications from various International Regulatory Authorities like - USFDA, MCC, UKMHRA, MOH – Belarus, INVIMA – Colombia, National Drugs Authority - Uganda, Food and Drugs Board - Ghana, MCAZ – Zimbabwe, Pharmacy and Poisons Board Kenya, Pharmacy Board Tanzania etc.

Walk in interview for M.Pharm, B.Pharm, M.Sc in Quality Control, Quality Assurance at Mankind Pharma

Mankind Pharma Is one of India's leading healthcare companies. Today, we have more than 14,000 employees and total turnover of INR 4500 Crore. Today, Mankind operates In 22 overseas countries across Asia, Africa, South East Asia and Gulf countries. The group has state-of-the-art manufacturing facility located at Paonta Sahib and Sikkim for manufacturing Solid Orals, Parenteral, Ophthalmic preparations and API manufacturing facility at Behror, Rajasthan. We have world class, state of the art R&D centre at Manesar, Delhi NCR. We are looking for young and dynamic personnel from Pharma background with proven track records, who have exposure to advance market operations (USFDA, TGA, EDQM, MHRA, etc) for Tablets, Capsules, Sterile Injectable, Potent products & Ophthalmic Products Formulation Unit at Paonta Sahib Location in Himachal Pradesh, for API unit at Sotanala-Behror (Rajasthan), for Development Quality Assurance at Manesar, Delhi NCR

Walk in interview for M.Pharm, M.Sc in Formulation QC at Syngene

Syngene International is one of India’s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

Post : Formulation QC - Stability Testing & Operations

Vacancy for QC Executive at Sigma Laboratories

Sigma Laboratories was founded in 1947 by Mr. Shrinivas Cowlagi and is now headed Mr. Dilip Coulagi who has over 40 years of experience in Pharmaceuticals. Sigma Laboratories is a name synonymous with quality both in India and abroad. By the late 1990s, in a market that accommodated 3800 players, Sigma was ranked amongst the top 60 pharmaceutical manufacturing companies in India.  Over the years, Sigma entered different therapeutic and manufacturing segments while building bonds of trust with its customers and establishing itself as a brand known for quality and reliability. In 2004, Sigma Laboratories Ltd. sold its domestic stable of brands as well as its national distribution business in order to downsize and focus solely on the export market.


UBM India announces 4th Annual Data Integrity, Reliability and Quality Metrics Workshop 2018

Data Integrity (DI) has become a focal point of FDA inspections, as is evidenced by the number of warning letters citing data integrity and the resulting number of import alerts. Company Quality Management Systems are being scrutinized as to how the integrity of raw data (both electronic and manual) generated in the Quality Control Laboratory and in Operations (Manufacturing and Engineering) can be assured. The FDA is now including recommendations for recipients to obtain 3rd party assistance when addressing DI issues.  Indicators of potential Data Integrity issues are an unreasonably low number of deviations, OOS incidents and EM excursions.  Regulatory non-compliance is always a serious area of concern for the Indian pharmaceutical sector. With 13 warning letters being issued in FY 2015 and 9 warning letters in FY 2016, Data Integrity still continues to be a severe problem to be tackled.

Recruitment for B.Pharm or M.Pharm at BUREAU OF PHARMA PSUs of INDIA - 4 posts | Government of India

BPPI is the implementing agency for Pradhan Mantri Bhartiya Janaushadhi Pariyojana of Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers, Government of India. The objective of the scheme is to make available quality generic medicines at affordable prices to all. BPPI is expanding its operations and has urgent requirement on following posts purely on contractual basis: