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 March 1995- July1995
Q A Technician 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