Billerica, Massachusetts, United States
*Chemistry/Quality Control professional with hands-on experience within a manufacturing environment *Performs work with an analytical, inquisitive, and solutions- driven mindset to completion *Proven ability to complete large volumes of highly detailed work accurately and thoroughly *Successfully completed inspections on mechanical and electrical manufactured products, within the medical device and oil home delivery industries Specialties: Analysis, Arcview, auditing, AutoCAD, calibration, chemistry, content and inventory management, customer relations, data entry, Environmental Science, Gas Chromatography, Geographic Information Systems, GIS, cGMP's, cGLP's, Karl Fischer, LIMS, laboratory, materials storage, MFGPro, Microsoft Excel, Microsoft Word, quality assurance, quality control, raw chemicals, SAP, scientist, SOP, SQL, technician, titration, UNIX
Successfully performed over 800 analytical chemistry tests, and inspections on raw materials, in-process samples, and finished products. Retrieved and reviewed important chemical information from Certificate of Analysis, product label, in-house reference checklist, and internet (as needed). Knowledgeable in documenting non-conformances. Proficient in Quality Management Systems and ISO 9001 standards.
• Received packages and performed incoming inspection on raw materials and processed them in the computer system (Syteline) regarding quantities and part numbers • Utilized calibrated testing equipment, standardized sampling plan, and company drawings to Inspect materials for dimensional accuracy, fit, and functional operation • Transacted and documented nonconformities in the system (MRB: Material Review Board) for further investigation and possibly sending them back to supplier (MRR: Material Review Report) • Collected previously received chemicals that expired and put in designated cabinet • Assisted with updating procedures, internal audits, and training new personnel • Completed problem solving and quality control duties as needed (ISO 9001) • All activities performed according to standard operating procedures (SOPs)
• Supervise fellow employees regarding the current Standard Operating Procedures (SOP) including the training and implementation of new or updated SOPs • Prepare various solutions according to the current SOP • Utilize laboratory instruments to build products; calibrate instrumentation as required • Document and analyze data obtained from in-process and finished products • Perform key quality control tasks on finished products and document inconsistencies • Maintain and order chemicals and supplies as needed • All duties performed within a cGMP and GLP environment