VANITA PATEL

***** ********* **,******,********-*8188

EMAIL: ac0bo5@r.postjobfree.com

PHONE: 609-***-****

CAREER OBJECTIVE:

To work as a professional candidate, using my knowledge in the field of pharmacy and to serve my best for the great success of the field. Seeking a position to utilize my knowledge, skills and abilities in the industry or pharmacy that offers competitive environment, a true profession, and opportunity to gain exposure to upcoming technologies and being resourceful, innovative and flexible.

WORK HISTORY:

a)QUALITY ASSURANCE SPECIALIST AT RARITAN PHARMACEUTICALS- 8,JOANA COURT, EAST BRUNSWICK, NJ, U.S.A(November-2015 to current)

WORKING ROLE:

Ensure, Evaluate and applies all quality assurance protocols for raw materials,manufacturing and packaging for all pharmaceutical dosage forms according to standard operating procedures in accordance with CGMP and USFDA guidelines.

Perform inspection, sampling and testing (where applicable) on all incoming raw materials, packaging components and returned goods following detailed written procedures.

Preparation of samples for chemical and, where required microbiological analysis and delivering them to QC Lab.

Inspection and test of packaging components utilizing various measuring devices such as scales, micrometers and height gauges to determine conformance with specifications.

Maintaining detailed records of sampling, inspections and testing activities.

Proper testing and disposition of return goods subject to further analytical testing, destruction, repackaging or return to inventory.

Perform room, equipment and packaging lines checks (where applicable) prior to each stage of manufacturing following detailed written procedures.

Conduct in process testing which may include but not limited to hardness, thickness, group weight, weight variation and variability.

Prepare controlled/uncontrolled/packaged finished product samples for QC lab and QA retains, following detailed documenting procedures.

Monitor facility environmental operating conditions and release of purified water system.

Perform in-process/coating validation sampling and tests.

Collection of samples for blend uniformity test utilizing applicable apparatus and methods.

Labeling component receipt, visual examination, counting, preliminary inspection and sampling.

Preparation of labeling components/inserts inspection reports, quarantine and release labels and maintaining incoming components log and corresponding inventory cards.

Issue of labeling components/inserts according to packaging order and regular monitoring and auditing label room.

Fill out the QA final labeled product inspection report, final line clearance which includes labeling and packaging reconciliation paperwork. Prepare QA in-process packaging reports and perform periodic bulk inspections and fill inspection reports.

Review all the documents and approve at the end of the finished goods.

b)REGISTERED PHARMACIST AT MORPHEOUS USHA FERTILITY CENTRE AND NURSING HOME- Anand, Gujarat, India (April-2011 to March-2013)

c)REGISTERED PHARMACIST AT ASHWINI MEDICAL MULTISPECIALITY CENTRE- Anand, Gujarat, India.

(April-2013 to August-2015)

WORKING ROLE:

Completed new and updated patient profiles, including lists of patients medications.

Checked prescriptions for appropriate dosage, drug interactions, allergies and contra indications before dispensing medicines.

Conducted patient counseling very politely and good care for patients.

Properly filled and dispensed prescriptions daily and checked labeled medication.

Managed drug and supply inventories.

Regularly stocked shelves rotated stock and checked for expired medications.

Conducted routine inspections of medication storage sites and properly maintained department equipments such as IV hoods.

Efficiently operated cash register and handled cash, checks, and charge transactions.

Properly handled billing system and yearly tax return systems.

Correctly completed pharmacy paperwork, including daily and weekly reports.

Good co-operated with other pharmacy staff and handled direct calls from doctors.

d)QUALITY CONTROL AND ASSURANCE INTERN AT VITAL FORMULATION PRIVATE LTD- V. V. Nagar, Gujarat, India.

(July-2010 to March-2011)

WORKING ROLE:

Performed all the operations for the quality of the product, Reviewed SOPs, batch records and test techniques according to CGMP formulations and ICH guidelines.

Checked and performed tests for incoming raw materials for production of tablets, capsules and liquids, done all the in process for all parameters for manufacturing, in process checking of packaging.

Performed quality control tests for finished products.

Ensured GMP conformity for raw materials and components disposal.

Provided assistance during product failures and complaints.

Provided research support and reminder of non-conforming materials.

Worked closely with Manufacturing and Quality Control to resolve open issues resulting from recorded reviews, internal audits of the facility, and deviation issues.

Reviewed and approved Validation and Technical Reports.

Reviewed fabrication records according to specifications and procedures.

EDUCATION:

Bachelor of pharmacy: completed four years from H. R. PATEL Institute of pharmaceutical education and research, Shirpur, Maharashtra, India. (North Maharashtra University, Jalgaon)

GPA: 3.44/4 scale and equivalency of Bachelors Degree in Pharmaceutical Science, USA (by WES)

SKILLS:

PHARMA SKILLS- Like retail pharmacy procedure, medication inventory management and maintenance quality, prescription drug labeling and interaction assessment, patient counseling.

OTHER SKILLS- Like self motivated, good decision making, self starter, and great communicator

ACHEIVEMENTS:

Conducted academic project on “Quantitative and qualitative analysis of underground water from different territory regions. “(Jan-2010 to june-2010)

Poster presentations at pharmacy weeks held by central pharmacy council.

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