QC

One of the leading manufacturers in pharmaceuticals. interme -diates fine chemicals company is establishing a modem R&D center,API and formulations manufacturing at TTC Navi Mumbai looking for cGMP.USFDA accreditation & looking for professionals with relevant

SMS Pharmaceuticals Ltd. is a global player in API manufacturing having a strong research and manufacturing team supported by state of the art facilities. What started off as a single facility - single product manufacturing company in 1990 grew to be a multi-location group having product list spreading across an array of therapeutic segments. SMS was given the export house status in the year 1997-98. SMS is currently a listed company having ever appreciating international and domestic customer base. Having four multi product facilities in operation and two research centers, SMS has truly graduated into big league with more than 1000 employees working for it.

A Leading Pharma Group with Global Presence and approvals from EU-GMP, MHRA-UK. ANVISA Brazil. PICS Ukraine .WHO Geneva, INVIMA Colombia. Exposure of working with Regulatory Approved facilities will be desired For our (Solid Oralsflnjectables) manufacturing Facilities at Baddi (H.P.) require:

Cadila Pharmaceuticals Ltd. (CPL) is one of India's most reputed, research-based, techno-savvy pharmaceutical companies with a focus in the area of Formulations & APIs and having its corporate office at Bhat, Ahmedabad and State-Of-Art manufacturing facilities compliant with USFDA, MHRA, TGA, MCA, MCC & WHO norms at Dholka, Ankleshwar, Kadi and Jammu.

Post : Quality Control - Sr Officer / Executive / AM /DM

Ipca has been continuously evolving as an integrated pharmaceutical company over 65 years. Ipca has an annual turnover in excess of Rs.3,120 Crores with over 350 formulations and 80 APIs for various therapeutic segments. We are committed to Research & Development and expanding our R&D capabilities to build a strong future. cGMP (current Good Manufacturing Practices) & Safety is a way of life. We are committed to further enhance cGMP and safety journey on continuous basis to deliver safe and quality products for mankind and to build a safe workplace for our employees. Our manufacturing facilities of bulk drugs at Ratlam have earned accreditation and approvals from the worlds most vigilant regulatory bodies.

We, Gufic Lifesciences Private Limited is coming with manufacturing facilities of PIC's, MHRA, USFDA requirement for formulation of Lyophilization injectables at Navsari (Gujarat) for which we are looking for competent candidates.

Sai Life Sciences delivers advanced Discovery, Contract Development and Manufacturing Solutions, through a broad suite of expert capabilities across the molecular lifecycle.  We are an ideal drug discovery, development and manufacturing partner. Our pharma and biotech clients gain clear competitive advantages through shorter time to market and risk minimization using our integrated and high-quality scientific services.

Post : Quality Control - 10 Opening(s)

In view of existing operational requirement and future expansions, it is proposed to recruit quality educational freshers from different locations across India, as a part of this we have planned Walk-in Interviews at HETERO(Corporate), Sanathnagar on 25th Nov, 2016 and the details are as follows: Requirement Details:

Post : Junior Officer/ Junior Research Associate/chemist - Formulations

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.

Post : Executive / Senior Executive