Neha Gupta

+1-615-***-**** adiav7@r.postjobfree.com 724 Buckhead Trail, Mount Juliet, TN 37122

CAREER OVERVIEW

Technical Manager with 1 year of experience with GMP documentation for Pharmaceutical Companies in India.

2.6 years of experience as a Sr. Lecturer in Pharmacy college teaching graduate and undergraduate students in India.

6 Months of experience as a pharmacist in India.

NABH (National Accredited Board of Hospitals) Certified.

Competent administrative professional supporting the underwriting process with effective document evaluation,

Report writing and file management skills.

Proficient in issuing quotes, gathering details and reviewing renewal requests.

Proficient in handling/entering data in data management system through various tools like SAP and applications

Like MS Office suite.

Proficiency in conducting periodic document audits and assist with internal audits of the QA and/or document management functions.

Very Good knowledge of Pharmaceutical Chemistry, Biochemistry, Pharmacology, Microbiology, Organic and Inorganic Chemistry.

WORK EXPERIENCE

1.

Company

Quality Services and Pvt. Ltd

Company

Company deals with ISO certification, WHO-GMP Certifications for pharmaceutical companies

Location

India

Role

Technical Manager

Duration

Nov 2011 to Dec 2012

Responsibilities

Generate and issue site-specific GMP associated documents as required to support the production function.

Coordinate the final review, revision, approval and issuance for all site-specific GMP associated documents.

Maintain current versions of site-specific GMP associated documents on the site on-line index.

Maintain all documentation related to new, revised and retired items on the Material Parts List.

Manage the audit of Batches of medicines.

Coordinate site specific document shipments for client reference or for off-site storage and/or retrieval

Prepare and provide documentation as required for internal and regulatory agency audits and maintain copies of reviewed documents

Conduct periodic document audits and assist with internal audits of the QA and/or document management functions.

Develop schedule for all GMP training at client; coordinate all activities related to these sessions

Evaluate effectiveness of training components and overall program

Maintain comprehensive matrix of employee GMP training requirements

Maintain training records (paper and/or electronic) for all client employees as well as contractors and/or consultants

Review documentation contained in GMP employee training records for compliance

Provide reports to management as necessary

Manage Offsite storage and retrieval of the documents.

Maintains a thorough knowledge of appropriate standard operating procedures (SOP’s).

Data review at a large scale within the system and entering at appropriate level using various tools and softwares like MS Excel and MS Word.

Data handling through various Data Management Systems like SAP (System Application & Products) data management system.

2. Sr. lecturer in Pharmacy College India.

College

Bharat College of Pharmacy

Work Location

Kurukshetra, Haryana, India

Role

Senior Lecturer

Duration

July 2008 to Oct 2010

Responsibilities

Supervise undergraduate or graduate students teaching pharma subjects

Supervised laboratory sessions.

Planned, evaluated, and revised curriculum, course content, course materials, and methods of instruction.

Compiled, administered, and graded examinations, or assigned this work to others.

Maintained regularly scheduled office hours to advise and assist students.

Prepared and delivered lectures to undergraduate or graduate students on topics such as Pharmaceutical Chemistry, Biochemistry, Pharmacology, Microbiology, Organic and Inorganic Chemistry.

3. Pharmacist.

Company

Govt Civil Hospital

Work Location

Ambala City, India

Role

Pharmacist

Duration

April 2005 to sep 2005

Responsibilities

Prepares medications by reviewing and interpreting physician orders; detecting therapeutic incompatibilities.

Dispenses medications by compounding, packaging, and labeling pharmaceuticals.

Controls medications by monitoring drug therapies; advising interventions.

Completes pharmacy operational requirements by organizing and directing technicians' work flow; verifying their preparation and labeling of pharmaceuticals; verifying order entries, charges, and inspections.

Provides pharmacological information by answering questions and requests of health care professionals; counseling patients on drug therapies.

Develops hospital staff's pharmacological knowledge by participating in clinical programs; training pharmacy staff, students, interns, externs, residents, and health care professionals.

Complies with state and federal drug laws as regulated by the state board of pharmacy, the drug enforcement administration, and the food and drug administration by monitoring nursing unit inspections; maintaining records for controlled substances; removing outdated and damaged drugs from the pharmacy inventory; supervising the work results of support personnel; maintaining current registration; studying existing and new legislation; anticipating legislation; advising management on needed actions.

Protects patients and technicians by adhering to infection-control protocols.

Maintains safe and clean working environment by complying with procedures, rules, and regulations.

Maintains pharmacological knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; participating in professional societies.

Contributes to team effort by accomplishing related results as needed.

EDUCATIONAL QUALIFICATION:

BACHELOR OF SCIENCE, PHARMACY FROM KURUKSHETRA UNIVERSITY- KURUKSHETRA, INDIA IN 2008.

Personal Details:

Name

Neha Gupta

Date of Birth

10/25/1986

Nationality

Indian

Work Authorization

H4 EAD

Neha Gupta

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