QC Sample Coordinator Resume Cranbury, NJ - Hire IT People

SUMMARY:

Seeking a challenging position where 10 years of QC/QA and over 20 years of administration experience will add value in the areas of Pharmaceutical industry.

SKILLS:

MS office, Windows, Microsoft Word, Excel, and Internet.

EXPERIENCE:

Confidential, Cranbury, NJ

QC Sample Coordinator

Responsibilities:

Receiving the Control/Non - control samples from production dept., R&D dept., Stability group and market perchased.
Having entries in respective log book and generate AR numbers and storing the samples product wise.
Controlled Samples log in Confidential Vault safe with generating “Inventory history records”
Handling and dispensing of Sample like tablets, capsules and powder on daily basis with logbook entries as per analyst’s requirements.
End of the day receive the all the issued controlled and non-controlled samples and re-storage after verifying the quantity.
Having update the online inventory of the quantity usage/balance of the samples in the computer.
Listing of the analyzed and released sample and discard it following respective SOP.
Organize all the Inventory History records and documents by product and prepare all the documents for the next day.
Samples sending out side Lab. for testing with entries in the documents.
All the released sample Lab report and related document submit to the Doc. Control Section.
Having physical inventory of the each samples at the end of the year with preparing a report of total samples during the year by” Received quantity” “Used quantity in Lab.,” “Discarded quantity” and “Balance quantity”.
Support Confidential activities as Confidential authorized personal which includes handling, distribution, physical inventory and rejection of controlled drug substances, reference standards and finished products.
Reviewing Confidential process for QC department and confirming with suggested SOP.
Reporting monthly and yearly inventory reconciliation of Confidential controlled substances to Material Management Department..
Preparation of purchase order for QC stuff as per purchase request.

Confidential, Somerset, NJ

QA Associate

Responsibilities:

Sampling of API .(Liquid, semi liquid and powder form)
Organization of documents like SOPs, Approved reports, references etc.
Daily check of stability chambers by changing charts and maintaining records.
Submission of documents/data records to Confidential at the Confidential audit.
Maintenance of retain sample storage with updating data.

Confidential, Somerset, NJ

QC Chemist

Responsibilities:

Receiving of Raw material, finished product, stability samples .
Analytical testing of API, finished product of softgel capsules.
Calibration of FTIR, UV, PH instruments as per schedule.
Organizing the QC documents like specifications, MSDS, analytical reports.
Coordinating with contract laboratories, for submitting samples and receiving reports.
Forwarded documents for review and filed with QA department on routine basis.
Coordinated with QA for Released sample documents archival procedure & data submission.
Disposal of Samples upon completion of all testing.
Maintenance of retain sample storage with updating data.

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Qc Sample Coordinator Resume

Cranbury, NJ

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