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Nalin. S. Desai 350D Lafayette Road, Apt 3b, Metuchen, NJ 08840 * mob (551) 358-7561 * email ndd277f8@westpost.

net * Home (732) 379-4385 Summary: A highly skilled professional with over 12 years of experience seeking opportuni ty in pharmaceutical environment. Hard working individual with dedication and co mmitment Professional Experience: Merck, Inc -Schering-Plough Corporation (Technisource Agency) Sept. 09 to Aug.2 010 Quality assurance inspector, Union, NJ * Perform various in-process tests, qualitative and quantitative, in order to en sure that the material meets quality standards. * Verify labeling, online printing including batch code/expiry and complete appr opriate batch documentations * Perform start of order line acceptance and post-order line clearance inspectio ns to ensure batch integrity * Review production area cleaning checklists for compliance and good documentati on practices * Monitor production and support areas for compliance as well as proper document ation Core Pharma & Wave Bio-Tech, GE Healthcare (Aerotek-Temp Agency) Aug.2008- Nov. 2008 Production Operator * Assembly of medical devices in clean dust free environment * Assembly of sealing and inspection of device Pliva Inc., East Hanover, NJ Dec.2001-Feb.2008 Packaging Operation: * Overseeing day-to-day label control operations * Managing inventory of labeling materials * Working under hard-pressed environment * Managing prism database * Issue and control of labels for ANDA/Stability batches * Line clearance, verification of dispensed materials * Overseeing day-to-day packaging operation * Flexible hard working and dedicated team player * Managing work force of 30 employees * Strong leadership to motivate team members in rapid changing environment * Ability to communicate effectively between work force and upper management * Knowledge of strategic planning, policies and principles to execute comprehens ive packaging operation Pliva Inc (Sidmak laboratories), NJ March.1998-Nov.2001 Q A Technician: * Line Clearance and component check of packaging line * Quality check, reading and observation during packaging run * Sampling, testing and approve of incoming packaging components and finished bo ttled products * Monitoring of chart recorder and data logger * Review and approve manufacturing and packaging batch record * Maintain database of production records * Review of standard operating procedures * familiar with CGMP regulations and SOPS'

Amide Pharma, NJ Q A Technician

March 1995- July1995 for Production Department.

Manufacturing (Pharmaceuticals) 1976- 1995 Manufacturing in Liquid Oral, External (Ointment & Liquid) & Capsules Department for different Pharmaceutical companies in India. Education: Bachelors of Science in Chemistry: Gujarat University, Ahmedabad, India Additional Skills: Knowledge of Computer Applications. Certified on problem solving skills and deci sion making (KT program) References upon request