Moustapha Soumah

** ****** ****

Phillipsburg NJ 08865

908-***-**** Day time

908-***-**** evening

ac328t@r.postjobfree.com

SUMMARY OF EXPERIENCE

Detail oriented, recognized as a self-starter with strong interpersonal and organization skills. Experience in the chemical and pharmaceutical manufacturing industries. Good Manufacturing Practice (GMP), Current Good Manufacturing Practice (cGMP), Standard Operation Procedures (SOP), FDA Regulations and extensive training with computers, OSHA, DOT, IATA and (CFR) 21 and 49 regulations. SPECIAL SKILLS AND EQUIPMENT HANDLING

Skilled with various plant manufacturing, production in chemical and pharmaceutical Industries, machine Operation for mixing raw materials, chemicals, Tablets, Gel, and capsules in Blisters troubleshoot and manor maintenance. PC uses Microsoft office; excel power point, word and outlook. Domestic and international dangerous Goods Electronics Shipment, Airborne, UPS, FedEx and Quick International on line. WORK EXPERENCE

January 2006 Celgene Corporation

Present Summit New Jersey

Lab Tech III

Responsible of daily interface between samples shipping and receiving domestic and international, commercial and clinical samples log into Lims and documentation according to (GMP) and (SOP) regulations and scheduling for analyst to test, Prepare sample submission form and testing requirement according to sample protocol to contract Labs for, Micro, Particle Size, Heavy Metal, Residue Ignition and water by Karl fisher testing, review test result and forward to Quality Assurance for record filing. Record and monitor all sample chambers for proper temperature according to (GMP) and (SOP) written procedures, track and manage sample records and handling laboratory responsibilities, Supply chain, purchasing lab equipment, instrument materials and general laboratory supply in work flow in Oracle. Handling and processing of customer complaint samples, processing includes using Global PTC data base, correspondence and preparation case closure using customer service data base. All activities are performed in accordance with applicable regulation, company polices and department STANDARD OPRERATION PROCEDURES for processing of customer complaint samples. Monthly stability pull, retains samples inspection and sample record keeping. Weekly Lab inspection to make sure the lab stay clean to pass FDA specifications. Ongoing training on (GMP’s), (cGMP’s) FDA (SOP’s) and OSAH safety regulations. Continue training on (SOP’s) (GMP’s) (cGMP’s). As required by company policy.

April 2005 Johnson & Johnson

January 2006 Raritan New Jersey

Laboratory Technician II

With all aspect of compound inventory and recording test results for scientist evaluation. Weighting of compounding, solubilized and process on conveyer machine for scientist to screen for drug processing.

November 2004 Centocor (Johnson & Johnson)

April 2005 Raritan New Jersey

Sample Administrator

Daily Interface between sample shipping and receiving domestic and international Sample documentation and registration according to (GMP) and (SOP) procedures. Sample Document and log in to LIMS and scheduling for analyst to test. Properly monitor sample chambers for temperature control according (SOP) written procedures sample retain and monthly visual inspection, monthly sample purge, monthly stability pull, create QC numbers for samples for easy tracking, recording and samples, laboratory record keeping. Have most experience in the manufacturing plant for soft Gel, tablets and capsules in blisters

December 1996 Fisher scientific Company Chemical Division April 2003 Somerville New Jersey.

Shipping Coordinator

Overall responsibilities including receiving and shipping chemicals from rail trucks and trucking companies, packaging and preparation of dangerous goods, for UPS, DHL Federal Express and truck ground shipping. Bill of lading preparation according to

(CFR-49), IATA and DOT shipping regulations.

OSHA, HAZMAT and DOT safety training.

Transfer from rail trucks to facility storage tanks, chemical inventory and proper waste storage procedures spill response and clean up following (MSDS) and OSHA safety regulations.

June 1986 PCA Packaging Corporation

November 1996 Piscataway New Jersey

Chemical Operator (compounder)

Responsible for daily plant work of mixing of raw materials and filling tubes, maintaining and keeping batch records for proper tracking product Code. Make sure product tanks and lines are clean to set up raw materials for another batch, milling and running of reactors centrifuges filter press. Visual inspection and appearance of finish product. Excellent documentation skills and attention to details, batch records keeping. Batch making and dropping, drying process, scrubber, pump, valves and gauges reading and control, hazardous and non-hazardous materials handling, bulk inventory and weighting of compounding on metric system and spill clean regulations. Skills & Qualifications:

Manufacturing Quality, Controls of Instrumentation, Equipment Maintenance, Manufacturing Experience, Assistance with maintenance of the finished product and raw material inventory receiving and inspection label verifications batch reconciliation and environmental monitoring.

Mechanical and Tools Inspection, Decision Making, Safety Management, Problem Solving, good Judgment and Job Knowledge.

Machine operating and trouble shoot, manor maintenance and some mechanical experience. Train new employees to meet company expectation. Training on (GMP),

(CGMP), FDA, OSHA, and HAZMAT safety regulations.

Education

September 1983 Winneba Specialist College Ghana West Africa August 1985 English, Math, Science and Chemistry.

(Associate Degree).

September 1979 Universal Technical, Accra Ghana, West Africa August 1983 English, Math, History, Geography, Science and Art. High School Diploma.

Interest

Reading, Music, Traveling and cooking.

Reference upon request.

Contact this candidate