Joyce Agyei
Quality Control Analyst at Pharma Medica Research Inc
Based in Mississauga, Canada
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Seniority
Staff
Department
Other
Location
Mississauga
Industry
Pharmaceutical Manufacturing
Company size
502
Contact information
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j•••••••@pharmamedica.com
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Background
About Joyce Agyei
Analytical Chemist with over 10 years of experience in Bioanalytical laboratory research performing; method development, method validation and method transfer for Bioequivalence studies in the pharmaceutical industry. Basic understanding of microbiology test methodologies. Interpersonal skills to develop and manage relationships with internal customers and suppliers. Comfortable to communicate effectively with clients in case of any clarification or an enquiry in regards to booking the samples in the system. Proficient in use of Internet and email communication skills. Knowledge in handling chemicals and titration chemistry. Proficiency in various techniques and operation of instrumentation (pH meter, viscometer, Karl Fisher apparatus, UV IR spectrophotometer, Chromatography instruments). Ability to apply knowledge of chemistry, math, instrumentation and statistics to complete tasks. Ability to work effectively in a team-based environment. Strong organizational, analytical and multi-tasking ability. Ability to troubleshoot and resolve issues. Excellent written and oral communication skills, particularly with analytical records, reports and investigations. Systems knowledge including LIMS, Microsoft Outlook, Word, PowerPoint and Excel. Hand/Eye coordination, ability to stand out, think outside the box. Able to read, understand and follow work instructions in a safe, accurate and timely manner. Proven ability to manage and coordinate multiple projects in a fast-paced, highly professional environment. Proven time management skills and a strong attention to detail. Works well under pressure. Strong understanding of the Clinical Laboratory operations and processes; provides leadership and train/manage personnel in Good Laboratory Practices (GLPs). Trained in WHMIS 2015 and occupational health and safety regulations as well as Good Manufacturing Practices (GMP) and FDA guidelines. Understanding and knowledge of MSDS (material safety data sheets). Experience in processing chromatographic data using Analyst Software (1.5.1) and Watson LIMS. Proficient in using Laboratory Data Management System (LDMS) for managing collections of biological specimens. Keyboarding skills of 50 – 60 wpm.
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