Quality Assurance Pharmacy Technician

Rovin Ranglall

**** ***** ******, ********* *****, NY.

Contact: 646-***-**** E-mail: *************@*****.***

OBJECTIVE

Quality Assurance Specialist/Batch Record Reviewer/Auditor with over 10 years' experience in Pharmaceutical Quality system, including in-process checks in manufacturing and packaging line, seeking a job with a Pharmaceutical manufacturing company where I can use my experience as a QA Specialist / Batch Record Reviewer / Auditor to become a valuable asset.

SUMMARY

Reviewing analytical batch manufacturing and packaging records as per cGMP.

Sampling of Raw material and packaging materials as per FDA guidelines.

Sampling of blend samples from production blenders.

Cleaning validation swab sampling as per cleaning validation protocol.

Release of production lines as per line clearance procedure.

Excellent work planning, time management, communication skills, Quality and result oriented, with the ability to work under pressure.

Strong computer skills for management of work, reports, data analysis and presentations (MS Word, MS

Excel, MS Power point)

EXPERIENCE

Quality Control Technician, Saint-Gobain Poestenkill NY (July 2018 to present)

Reviewing Manufacturing Batch Records

A

Reviewing Packaging Batch Records

Reviewing Finished Product Certificate of Analysis

Releasing Finished Product

Preparing and filing customer complaint reports

In process quality checks in manufacturing.

Sampling of packaging and raw materials.

Conducting internal quality audits and checks.

Quality Assurance Specialist/Batch Record Reviewer, Albany Molecular Research Inc. (January 2018 to July 2018)

Reviewing Manufacturing Batch Records (Commercial, validation and Submission)

Reviewing Packaging Batch Records (Commercial and Submission)

> Reviewing Finished Product Certificate of Analysis

Reviewing Purified Water Certificate of Analysis

Releasing Finished Product

Reviewing Cleaning Validation Report

Rovin Ranglall

1057 Keyes Avenue, Niskayuna 12309, NY.

Contact: 646-***-**** E-mail: *************@*****.***

Preparing and filing customer complaint reports

Preparing, Follow up and closing Deviation Reports in STRATAS/MASTER CONTROL

Issuance of Change Control and Approval in STRATAS/MASTER CONTROL

Follow up and Approval of CAPA in STRATAS

Quality Assurance Auditor, Anneal Pharmaceuticals LLC, Hauppauge (January 2016 to September 2017)

Reviewing Manufacturing Batch Records (Commercial, validation and Submission)

Reviewing Packaging Batch Records (Commercial and Submission)

Reviewing Finished Product Certificate of Analysis

Reviewing Purified Water Certificate of Analysis

Releasing Finished Product

Reviewing Cleaning Validation Report

Preparing and filing customer complaint reports

Preparing, Follow up and closing Planned Deviation Reports

Issuance of Notice of Investigation and Planned Deviation Number

Quality Assurance Auditor, Polygen Pharmaceuticals LLC, Deer Park, New York (March 2013 - January 2016)

Reviewing of batch records and issuance of batch manufacturing records.

In process quality checks in manufacturing.

Sampling of packaging and raw materials.

Cleaning validation sampling.

Line clearance.

Documentation practices as per company's SOP and cGMP regulation.

Conducting internal quality audits and checks.

Label control and inventory.

Warehouse Supervisor, Polygen Pharmaceuticals LLC, Deer Park, New York

Shipping and Receiving

Preparing Packing Slips

Maintaining Inventory

Quality Assurance Specialist, Amneal Pharmaceuticals LLC, Hauppauge (May 2011 - Feb 2013)

Reviewing of batch records, assuring accuracy and completeness.

Rovin Ranglall

1057 Keyes Avenue, Niskayuna 12309, NY.

Contact: 646-***-**** E-mail: *************@*****.***

Production in- process QA testing.

Sampling activities pertaining to raw and packaging materials.

Assuring cleaning of production equipment by swab sampling as part of cleaning validation studies. Issuing line clearance before start of any production activities.

Maintaining all documentation as per GMP requirements following the Standard operating procedures. Participating in internal quality audits as part of routine in-house audits.

Issuing and maintaining the labels records.

EDUCATIONAL CREDENTIALS

CXC (Seven subjects at the Caribbean Examination council) High School Diploma from US.

CERTIFICATIONS

Certificate in information Technology

Certificate in Process Improvement - Stoney Brook University

WCM TOOLS - OPL, 6M, Go Fast Approach and 5 Why.

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