Teva Pharmaceuticals Ltd. (NASDAQ: Teva) is a leading global pharmaceutical company, committed to increasing access to high-quality health care by developing, producing and marketing affordable generic drugs as well as innovative and specialty pharmaceuticals and active pharmaceutical ingredients Headquartered in Israel, Teva is the world's largest generic drug maker, with a global product portfolio of more than 1,250 molecules and a direct presence in approximately 60 countries. Teva employs about 40,000 people around the world and reached $ 16.1 billion in net sales in 2010. Since August 2010 ratiopharm is a part of Teva group. Ratiopharm India private limited has established a Research & Development centre & a Manufacturing unit at Verna Goa and Quality Assurance, Regulatory affairs, & LIMS support organizations at Mumbai.

Research Associate / Research Scientist / Senior Research Scientist / Assistant Manager
M.Pharm / M.Sc. / PhD (Analytical Chemistry) with 3-9 years experience in reputed pharmaceutical companies with experience in Method development and validation for assay / related substances / Dissolution / UOC / residual solvents using UPLC/ UV / GC / Dissolution apparatus. Experience of working & handling various dosage forms such as solids / liquids / creams in a regulated environment is essential.

Executive / Assistant Manager - Project Management
The person will be required for project management, reviewing & monitoring of timelines, liaison with regulatory and API sourcing, monitoring project proposals & budget timelines for US region. The candidate should have a degree in Pharmacy, preferably with a diploma in Management and 3-5 years experience in a similar role in a reputed Pharma company, be proficient in document management & exposed to the use of project management software.

Executive / Sr. Executive - Quality Assurance Support
The person will be required for compiling, maintaining, evaluating of Annual Product reviews (APR) & compiling related quality data, technical documents, documentation & analysis for the products manufactured at various International Sites. The person should be graduates in Pharmacy with 2-3 years of experience in Quality Assurance, Quality Control or Manufacturing, preferably in a similar role, with a reputed Pharmaceutical Company in a regulatory environment.

Executive / Associate - LIMS
B.Sc. / M.Sc. (in Chemistry) with 2-3 years of experience in Quality Control or Quality Assurance in a Pharmaceutical Company. The candidate should be conversant with analytical methods, product specifications, Monographs, USP/ EP compendia, SOPs, Good documentation practices and have good strong computer and data entry skills. Experience of working with LIMS software would be preferred.

The candidates for all the positions should have proficiency in computer skills, sound knowledge of GMP documentation, GMP & GLP Guidelines, Interpersonal & communication skills for interacting with international teams and exposure to regulatory environment.

Production & Validation Process Manager
The key role will be to support & Supervise validations & Production process improvements at TEVA's strategic Contract Manufacturers in India to ensure that all validations are completed as per TEVA's procedures and standards. Will also support resolution of production related issues, provide Operational support of products transfers & perform routine onsite visits to monitor Production & Quality standards. Should be a Pharma Graduate/ Postgraduate with 7-10 years direct experience in a Validation or production managerial role in Pharmaceutical Industry for regulated markets. He should have knowledge on process validation procedures for scale-up, scale -down, post marketing operational validations and submission batches requirements. Based at Mumbai, the job will involve travel to different Contract Manufacturers.

Assistant Manager / Manager Quality Audit - API
The person will be required to perform Quality auditing of API and Intermediate manufacturers, prepare audit reports, organization and management of audits and coordination with the manufacturers. Should be a B.Pharm / M. Pharm / M.Sc with about 5-10 years experience in similar functions in a Pharmaceutical Company with good knowledge of API manufacturing, Quality systems and cGMP. The person will be based at Mumbai.

Assistant Manager / Manager Quality Audit - Formulation
The person will be required to perform Quality auditing of API and Intermediate manufacturers, prepare audit reports, organization and management of audits and coordination with the manufacturers. Should be a B. Pharm / M.Pharm / M.Sc with about 5-10 years experience in similar functions in a Pharmaceutical Company with good knowledge of API manufacturing, Quality systems and cGMP. The person will be based at Mumbai

Assistant Manager / Manager Quality Audit - Formulation
The person will be required to perform FG facilities audits prepare audit reports, organization and management of audits and coordination with the manufactures. Should be a B. Pharm / M.Pharm/ M.Sc. - Microbiologist with about 5-10 years with knowledge and experience in auditing engineering/ validations and QC/ microbiology laboratories. The person will be based at Mumbai.

Interested candidates may please send their detailed bio-data indicating the position applied by courier / post / e-mail within seven days to the following address: