InvaGen Pharmaceuticals, Inc., on associate company of HETERO, GROUP, INDIA is a fast growing generic pharmaceutical company located in Long Island, New York, USA. Our core business is in the areas of Development, Manufacturing, Marketing and Distribution of high quality and cost-effective generatic prescription medicines. InvaGen has drug product development and commercial operations at three different facilities in Long Island, New York, USA.

To strengthen its Manufacturing Operations 'InvaGen" is looking for the dynamic and result oriented Pharma Professionals to be based at its finished dosages facility located in Long Island, New York, USA.

General Manager - Production (Formulations)
M.Pharm/ B.Pharm with 10-15 years of relevant exposure with a large Pharma company. Must have worked for atleast 5 years in a Senior Managerial position with great commitment to Qualit, Productivity and Safety. Candidate must have proven track record of achieving production targets, optimize plant capacities, winning mind set, high level of business / technical acumen, strong interpersonal skills, initiative and risk taking ability is required as a core competency. The incumbent will head the complete formulations (Solid Orals) facility.

Dy. General Manager/ Manager/ Deputy Manager - Production (Formulations)
M.Pharm/ M.Sc. with 8-15 years of experience in handling the Production department independently in a tablet/ capsule manufacturing USFDA certified formulations facilities. Exposure to the international audits like USFDA, EMEA, TGA, TGA, ANVISA, MCC etc as a front leader is essential.

Dy. General Manager/ Manager / Deputy Manager - QA (Formulations)
M.Pharm/ M.Sc./ B.Pharm, with 8-15 years of experience in IPQA, Analytical Documentation, validation/ qualification on exposure to the international audits like USFDA, MHRA, TGA, ANVISA, WHO etc as a front leader is essential.

Dy. General Manager/ Manager/ Deputy Manager - QC & Analytical Development (Formulations)
M.Pharm/ M.Sc./ B.Pharm with 8-15 years of experience in handling the Quality Control & Analytical Development related activities in solid orals. Exposure to the international audits like USFDA, EMEA, TGA, ANVISA, MCC etc as a front leader is essential.

We provide professionally stimulating and challenging work environment for the people to excel. Salary should not be a constraint for the right candidate.

Candidates meeting the above requirements may forward their resume mentioning the position applied for in the subject line.

Candidate those who are interested should be available for a discussion during the 3rd week of September 2010 at Hyderabad