Kategorien durchsuchen
Entdecken
Fiverr Pro
Deutsch
$
USD
Shakeela Shaif
@shakeelashareef
Chemist,Pharmaceutical and Agricultural Industry Experience
Pakistan
Englisch
Über mich
I am a chemist with 5 years of industrial experience in the pharmaceutical and agricultural sectors. I have hands-on experience with SDS/MSDS, COA, SOPs, QA/QC documentation, regulatory compliance, DRAP submissions, dossier preparation and review, and agricultural chemical documentation. I provide support with chemical documentation, regulatory documentation, scientific research, literature reviews, and chemistry and biology-related academic assistance. I focus on accuracy, confidentiality, and well-organized work.
Kompetenzen
Shakeela Shaif
offline •
Meine Dienstleistungen
Zertifizierungen und Vorschriften
I will provide pharmaceutical regulatory and quality support
Arbeitserfahrung
Chemist
Group • Vollzeit
Oct 2024 - Jan 2026 • 1 yr 3 mos
Performed advanced analysis of micronutrients, fertilizers, and pesticides using GC, HPLC, UV-Vis, Kjeldahl apparatus, atomic absorption, flame photometry and hands-on experience with LCMSMS. Assisted in the development and optimization of new testing methods and lab technologies. Ensured compliance with ISO 17025 and ISO 9001 standards, maintaining detailed documentation of lab procedures and results. Contributed to quality audits and lab accreditation processes, managing records as per regulatory requirements. Implemented best lab practices and protocols, ensuring accuracy and efficiency in testing and reporting using MS Word and Excel.
Citi Pharma Limited
Vollzeit • 3 yrs 3 mos
Quality Control Analyst
Jan 2023 - Oct 2024 • 1 yr 9 mos
Performed quality control testing of raw materials, in-process samples, and finished pharmaceutical products. Conducted chemical and physical tests according to approved SOPs and pharmacopeia standards. Prepared and analyzed samples using laboratory equipment and instruments. Maintained accurate laboratory records, test results, and documentation in compliance with GMP requirements. Monitored product quality and identified deviations or out-of-specification (OOS) results. Assisted in investigations of quality issues and implemented corrective and preventive actions (CAPA). Followed Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and laboratory safety procedures. Coordinated with production and quality assurance teams to ensure compliance with quality standards. Supported internal and external audits by maintaining complete and organized quality documentation.
Regulatory Affairs Officer
Jul 2021 - Jan 2023 • 1 yr 6 mos
Ensuring compliance with regulatory requirements and standards. Managing and preparing dossiers, such as the Common Technical Document (CTD) and Drug Regulatory Authority of Pakistan (DRAP) submissions. Reviewing documentation for regulatory compliance. Preparing dossiers for export purpose and DRAP submissions. Keeping up-to-date with regulatory guidelines and changes in regulations. Manage queries from DRAP regarding Dossiers shortcomings. Responding to regulatory inquiries and addressing any compliance issues. Responding to DTL and PQCB letters. Participating in regulatory inspections and audits. Ensuring the accuracy and completeness of regulatory documentation. Perform other tasks as delegated by Regulatory Management.
