Bilal Abbas

Experience

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  Nuclear Medicine, Oncology and Radiotherapy Institute (N.O.R.I), Islamabad

  Jan 2011 - Feb 2011

  Trainee Pharmacist

  Cancer Chemotherapy and Radio pharmaceuticals.

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  Shaukat Khanum Memorial Cancer Hospital & Research Center

  Jan 2012 - Jan 2012

  Trainee Pharmacist

  During my tenure at SKMH, Lahore, I had the privilege of being part of an esteemed healthcare institution committed to providing world-class cancer care and treatment. As a trainee pharmacist, I actively contributed to the pharmacy team's efforts to ensure safe and effective medication management for patients while gaining invaluable experience and knowledge in the field of pharmacy.Key Responsibilities:🔵 Medication Dispensing: Accurately dispensed medications as per prescriptions, following strict protocols and safety measures to guarantee patient well-being.🔵 Patient Counseling: Provided essential information and counseling to patients and their families regarding medication usage, potential side effects, and adherence to treatment plans.🔵 Inventory Management: Assisted in maintaining optimal inventory levels, monitoring stock, and ensuring the availability of essential medications.🔵 Prescription Review: Conducted thorough reviews of prescriptions to identify potential drug interactions, allergies, and dosage discrepancies, collaborating with healthcare professionals to resolve issues.🔵 Patient Safety: Demonstrated a strong commitment to patient safety by participating in medication error reporting and implementing safety measures to prevent adverse events.🔵 Emergency Support: Collaborated with the healthcare team during emergencies, providing rapid access to critical medications and ensuring their safe administration.🔵 Continuous Learning: Actively engaged in ongoing professional development by attending training sessions, seminars, and workshops to stay updated with the latest advancements in pharmacy practice.🔵 Team Collaboration: Worked closely with pharmacists, nurses, and physicians to foster a multidisciplinary approach to patient care, contributing to improved treatment outcomes. Show less

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  The SEARLE Company Ltd.

  Jan 2012 - Jan 2016

  Production Executive

  I had the distinct privilege of leading and managing the production of finished pharmaceutical products in strict adherence to cGMP standards. This role allowed me to play a pivotal part in ensuring the delivery of safe, effective, and high-quality pharmaceutical products.Key Responsibilities:✔️Production Management: Spearheaded the entire production process, from planning and scheduling to execution and quality control, to ensure seamless and efficient production operations.✔️cGMP Compliance: Diligently adhered to cGMP standards and guidelines, fostering a culture of compliance and quality excellence throughout the production facility.✔️Process Optimization: Continuously identified opportunities for process improvement, efficiency enhancements, and cost reduction while maintaining product quality and safety.✔️Team Leadership: Managed and motivated a dedicated team of production staff, providing guidance, training, and support.✔️Quality Assurance: Collaborated closely with the Quality Assurance department to implement and maintain stringent quality measures and ensure that all products met regulatory and quality standards.✔️Inventory Management: Oversaw inventory levels and production planning to meet customer demand while minimizing wastage and maintaining optimal stock levels.✔️Safety and Compliance: Ensured that all safety protocols and compliance standards were met, creating a safe working environment for employees and protecting the integrity of the products.✔️Continuous Improvement: Initiated and participated in continuous improvement projects, driving innovation and excellence in the production process.✔️Cross-functional Collaboration: Collaborated with other departments to ensure seamless integration of activities and alignment with organizational goals.✔️Reporting and Documentation: Maintained accurate production records, reports, and documentation required for audits, regulatory submissions, and internal reviews. Show less

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  EY

  May 2017 - Jul 2019

  Senior Consultant GxP | GMP Auditor | Life sciences Advisory

  Roles and Responsibilities:As a Senior Consultant and GMP Auditor in the Lifesciences Advisory division of EY, I have dedicated my career to ensuring the highest standards of pharmaceutical quality and regulatory compliance. With a wealth of experience, I have undertaken the critical responsibility of conducting third-party risk-based regulatory inspections of over 300 drug manufacturing units, consistently benchmarking them against the rigorous standards outlined in the WHO GMP guidelines.My role has encompassed all facets of the pharmaceutical industry, covering a diverse range of products, including Finished Pharmaceutical Products for both human and animal consumption, vaccines, semi-basic, and basic pharmaceutical manufacturers. My expertise lies in meticulously evaluating and enhancing compliance across the key areas of Good Manufacturing Practices (GMP)🚀 Risk Mitigation: Collaborated closely with clients to identify and address potential compliance risks, providing strategic recommendations to enhance GMP compliance and minimize regulatory vulnerabilities.📋 Client Relationships: Fostered strong client relationships by delivering high-quality audit and advisory services.📊 Team Leadership: Acted as a leader within the team, guiding junior consultants and auditors, sharing knowledge, and contributing to the professional development of colleagues.🕵️ Industry Expertise: Stayed abreast of evolving regulations, industry trends, and emerging best practices in the pharmaceutical and life sciences sectors to provide informed guidance to clients.📝 Reports and Documentation: Produced detailed inspection reports and compliance documentation, offering clients clear insights into the current GMP status and actionable recommendations for improvement.🔎 Continuous Improvement: Committed to ongoing self-improvement and professional development, participating in relevant training and certification programs to remain at the forefront of the industry. Show less

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  Mustafa Khan & Company (Chartered Accountants)

  Jul 2019 - Sept 2020

  Head Pharmaceutical Advisory

  Key Responsibilities:As the Head of Pharmaceutical Advisory at Mustafa Khan & Company, I bring a wealth of experience in ensuring compliance with current Good Manufacturing Practices (cGMP) and providing strategic guidance in the pharmaceutical sector. My role involves overseeing and advising on various aspects of regulatory compliance, quality assurance, and risk management within the pharmaceutical industry.Conducted thorough assessments of manufacturing facilities to ensure compliance with cGMP regulations and other relevant standards.Provided strategic guidance to pharmaceutical companies on quality management systems, risk mitigation, and regulatory compliance.Worked closely with clients to identify areas for process improvement and efficiency enhancement.Developed and implemented tailored solutions to address specific challenges in pharmaceutical manufacturing.Conducted training sessions and workshops on cGMP, quality risk management, and regulatory compliance for client teams.Collaborated with regulatory authorities to stay abreast of industry changes and updates, ensuring clients were well-informed and prepared for evolving regulatory landscapes.Key Achievements:Spearheaded cGMP consultancy services, facilitating clients in aligning their manufacturing processes with international quality standards.Led a team to develop a comprehensive Quality Risk Management System at Ferozson Laboratories, a project that significantly enhanced the company's quality control procedures.Collaborated with cross-functional teams to assess, identify, and mitigate potential risks in pharmaceutical manufacturing processes, ensuring adherence to global regulatory requirements. Show less

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  Shaigan Pharmaceuticals (Pvt) Ltd.

  Sept 2020 - now

  Manager QA (DI & DG, QRM, Audit, PQS / QMS, VQ)

  I am a dedicated and results-driven Quality Assurance Manager with a proven track record in the pharmaceutical industry. My expertise lies in developing, implementing, and maintaining robust Pharmaceutical Quality Systems (PQS) to ensure the highest standards of product quality, compliance, and patient safety.Key Responsibilities:🔍 Pharmaceutical Quality Systems (PQS): Leading the design, implementation, and continuous improvement of PQS to comply with international regulations and standards.📋 QMS Compliance: Overseeing Quality Management System (QMS) compliance, including documentation control, change management, and ensuring adherence to SOPs.🔐 Data Integrity & Data Governance: Implementing and monitoring data integrity policies and practices to safeguard critical data, ensuring its accuracy, completeness, and reliability.📝 Document Control: Managing document control processes, including creation, review, approval, and archiving of documents in alignment with GxP requirements.🚀 Quality Risk Management: Implementing risk-based approaches to identify, assess, and mitigate quality risks across the product lifecycle.🔎 Product Quality Reviews (PQR): Conducting comprehensive PQRs to evaluate product quality, identify trends, and drive continuous improvement.🕵️ Self Inspection: Leading self-inspection programs to ensure ongoing compliance with regulatory requirements and best practices.🔍 Root Cause Analysis (RCA) & CAPA: Proactively addressing deviations and quality issues through effective root cause analysis (RCA) and corrective and preventive action (CAPA) programs.📊 Quality Audits / Vendor Audits: Planning and conducting internal and external quality audits to assess compliance with regulations and internal quality standards.My passion lies in driving a culture of quality and compliance, fostering cross-functional collaboration, and ensuring that every product leaving our facility meets the highest standards of safety and efficacy. Show less

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  Explotek

  Sept 2023 - now

  Co-Founder

  Explotek is a startup, with its innovative vision and unwavering commitment to excellence, is poised to reshape the landscape of life sciences through the seamless integration of technology.Slogan: "Technology-Driven Life Sciences Solutions"In a rapidly evolving world where technology is the driving force behind advancements in life sciences, Explotek stands as your beacon of knowledge, inspiration, and collaboration. Join us today and be part of a vibrant community that is pushing the boundaries of what's possible in the exciting intersection of technology and life sciences.Explotek: Where Technology Meets Life Sciences, and Possibilities Are Limitless. Show less