Bliss Emeh
Wales,UNITED KINGDOM
Summary
A results-driven pharmaceutical scientist with specialized expertise in Quality Control (QC), pharmaceutical analysis, and regulatory affairs. Proficient in using advanced analytical techniques, including LCMS, HPLC, FTIR, UV, Karl Fischer, GCMS, with a strong understanding of cGMP, GDPR, GLP, MHRA, ICH/GCP regulated procedures, and SOPs. Experienced in performing routine and non-routine analysis, maintaining quality documentation, ensuring product quality and adhering to Health, Safety, and Environmental (HSE) guidelines. Consistently improve processes by identifying and resolving issues through meticulous analysis and testing. Ability to work collaboratively in team settings, utilising advanced laboratory techniques and maintaining stringent standards to guarantee product integrity.
Overview
7
7
years of professional experience
Work History
Quality Control Analyst Level II
PCI Pharma Services
06.2023 - 03.2025
- Perform routine testing and analysis on raw materials, in-process samples, and finished products
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory guidelines (e.g., FDA, EMA, ISO)
- Operate and maintain analytical instruments such as HPLC, GC, UV-Vis, FTIR, and pH meters
- Ensure proper calibration and validation of laboratory equipment
- Document and report test results accurately, following standard operating procedures (SOPs)
- Identify deviations, out-of-specification (OOS) results, Events, and conducted investigations on root cause, implemented appropriate and preventive actions throughout development process
- Conducted method development and validation, validation parameters which includes linearity, forced degradation, method precision/responsibility, LOD/LOQ, Accuracy
- Participated in maintaining stability databases, performing data trending and statistical analyses
- Engaged in equipment troubleshooting, fostering a culture of continuous improvement and knowledge sharing
- Familiar with different laboratory information management systems for sample result entry, execution of electronic assay forms etc
- Support stability testing and environmental monitoring programs
- Participate in internal audits, quality assurance reviews, and regulatory inspections
- Work collaboratively with production, R&D, and regulatory teams to maintain product quality
- Contribute to continuous improvement initiatives for efficiency and quality enhancements
QC Analyst
Trinacx Pharmaceutical Limited
03.2020 - 08.2021
- Perform Laboratory work and data analysis to high standard in compliance with all pertinent protocols and SOPs
- Ensures that all daily operations are carried out in compliance with GMP/GLP regulations
- Adhere to appropriate documentation to quality standard operating procedures, COSHH/BIOCOSHH, GMO assessments, and risk Assessments
- Proficient in conducting testing assays such as ELISA, polymerase chain reaction test (PCR) and flow cytometry within the laboratory
- Encouraged colleagues to uphold HSE standards in regular business operations, fostered positive behavior, and complied with HSE regulations
- Provided up to date quality documentation of all manufacturing process data and regulation submissions
- Executing clinical and pharmaceutical task ranging from stocking supplies, verifying specifications, equipment sterilization, operations, troubleshooting, laboratory maintenance such as laboratory housekeeping, stock control, and record-keeping
- Facilitate investigation and (CAPAs) processes to eliminate causes of non-conformities or other undesirable situations
- Report back to head of department and managers on frequent basis about the progress of research and projects
Pharmacist
University of Calabar Teaching Hospital UCTH
07.2019 - 01.2020
- Preparing and dispensing medications
- Resolving drug-related problems such as drug interactions, and formulary issues and performing medication therapy management (MTM)
- Implementing medications synchronization
- Ordering stock and organizing inventory
- Counselling patients on prescription medications and OTC products including medical devices
- Applied correct pricing structures and controls for pharmacy, POM and GSL products
- Supervised medicines supply chain and ensure appropriate documentation processes and regulations were followed
- Collaborate with doctors, nurses and other healthcare professionals regarding prescription medications and concerns
- Monitor and report adverse drug reactions (pharmacovigilance)
Pharmacist
Ternopharm pharmaceuticals
Ternopil
07.2018 - 08.2019
- Responsible for day-to-day operation of the pharmacy including regular control and recording of stock list, review of medical prescription and issuing medications and staff supervision
- Resolving drug-related problems such as drug interactions, and formulary issues and performing Medication Therapy Management (MTM)
- Implementing medication synchronization
- Ordering stock and organizing inventory
- Counselling patients on prescription medications and OTC products including medical devices
- Applied correct pricing structures and controls for pharmacy, POM and GSL products
- Prepared unit dose packaging
- Analyzed patient profiles
- Assessed labs for proper medication use
- Recommended alternative drug treatments
- Intervened for medication errors or drug interactions
- Stored medication according to specific temperature instructions
Education
MSc - Pharmaceutical Science
Robert Gordon University
Aberdeen, Aberdeen CityBSc - Pharmacy
Ternopil State Medical University
Ternopil UkraineSkills
- HPLC, LC-MS, FTIR, UV-Spec, NMR Spectroscopy, TLC, Empower Citrix, LIMS, SPC,
- Advanced Knowledge of Microsoft Windows environment, windows server and office package (Word, Excel, Access and PowerPoint), Mac OS/iOS environment
- Equipment calibration expertise, Process validation mastery, Data interpretation aptitude
- Excellent knowledge and proven record of compliance with GMP, manufacturing standard procedures and legal regulations
- Proven ability to produce high quality technical, oral and written communications
- Good interpersonal skills, conflict resolution and relationship management
Accomplishments
- NMR Spectroscopy workshop, 04/01/18, This workshop gave a valuable opportunity to gain knowledge and practical experience in NMR data processing, spectral analysis, and interpretation.
- Students Scientific Society, Association of young medical professionals of Ternopil region, 04/01/18, A workshop aimed to develop the scientific capabilities of medical/pharmaceutical students to improve their professional skills.
- 8th International Christian Medical Conference (ICMA), 10/01/17, This conference prepares students and healthcare professionals for academic excellence with a Christian Perspective to bring healing to the whole person and to impact the world.
- The Nigerian community variety/awards night (Committee Member), 12/01/17, An award show held by the Nigerian student’s association Ternopil Ukraine to acknowledge and encourage students and committee members for their hard work throughout the academic year.
Affiliations
- Movies, Photography, Nature, Travelling, Board games
Timeline
Quality Control Analyst Level II
PCI Pharma Services
06.2023 - 03.2025
QC Analyst
Trinacx Pharmaceutical Limited
03.2020 - 08.2021
Pharmacist
University of Calabar Teaching Hospital UCTH
07.2019 - 01.2020
Pharmacist
Ternopharm pharmaceuticals
07.2018 - 08.2019
MSc - Pharmaceutical Science
Robert Gordon University
BSc - Pharmacy
Ternopil State Medical University
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