Jashraj Sachdeva Quality Assurance, Advanced Industrial Pharmacy
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I focus on practical, real-world learning where concepts are linked directly to how they are applied in the pharmaceutical industry. Instead of just memorizing, my students learn by understanding processes, solving case studies, and applying knowledge to real-life situations.

Methodology I Use -
1. Case Study Based Learning: Using examples from UK and Indian pharma industry (QA, R&D, GMP audits).
2. Problem-Solving Sessions: Students learn how to think like industry professionals.
3. Interactive Discussions: Encouraging questions and real-time problem analysis.
4. Industry-Oriented Assignments: Preparing reports, audit checklists, and project simulations.
5. Blended Approach: Combining academic theory with industrial applications so students can excel in both exams and jobs.

Why I Am Different -
(A) Global Exposure: 5 years in UK pharma QA and R&D gives me international insight and global knowledge.
(B) Academic + Industry Balance: Experience as Assistant Professor in an Indian pharma university means I understand how students learn best.
(C) Focused Mentorship: I don’t just teach subjects, I guide students on career paths, interview prep, and skills needed for pharma jobs.
(D) Specialized Subjects: QA, auditing, industrial pharmacy, and management are my core strengths—areas where I’ve both taught and worked extensively.
(E) Student-Centric Approach: Every session is tailored to student needs—whether exam preparation, project guidance, or industry readiness.

Why I am the best fit -
I bring the rare combination of academic knowledge and global industry experience, which helps students not only score better in exams but also stand out in careers. My teaching bridges the gap between classroom learning and industry requirements, ensuring students are fully prepared for the future.

Subjects

  • QA (Quality Assurance) Beginner-Expert

  • Pharmaceutical Management Beginner-Expert

  • Advanced Industrial Pharmacy Beginner-Expert

  • Pharmaceutical Audit Handling Beginner-Expert

Experience

  • Quality Assurance Officer (Aug, 2024–Present) at NHS England
    - An authorized Releasing officer, involved in releasing batches and named patient-manufactured products under the MHRA MS license.
    - Involved in Release of Radiopharmaceutical products and work in the Quality Assurance laboratory undertaking quality control analysis (including Radiopharmaceutical Purity testing) and checks on products made in the manufacturing units, raw materials and unlicensed medicines.
    - Involved in quality systems and documentation management systems.
    - Involved in the release of specials and imports as per the department's procedures.
    - Participate in the program of environmental monitoring when required.
    - Raising and completing out-of-specification investigation forms obtained from environmental monitoring or chemical testing.
    - Involved in responding to customer complaints and undertaking drug defect investigations for Trust manufactured products.
    - Complete all paperwork accurately and legibly so that it may be audited as appropriate in compliance with ALCOA plus.
    - Carry out QC checks on over-labelled and re-packed products and on prepared batches of CIVAS and Cytotoxic products.
    - Involved in certification of the finished product batch signifying that the batch is in compliance with GMP and the requirements of its MS.
    - To raise deviations followed by taking immediate actions and conduct risk/impact assessment, root cause analysis and implementing CAPA.
    - Involved in effective implementation of Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).
  • Research and Development Scientist (May, 2021–Jun, 2024) at Bristol Laboratories Limited
    Involved in validations and analysis of the research drugs ensuring the parameters of precision and accuracy as per ICH guidelines.
    - Communicating about technical and complex information clearly with the team and stakeholders
    - Involved in data management of the bio-equivalence studies/ Clinical trial studies, stability parameters and therapeutic effect of the drug on the patients for the projects.
    -Provided advice and guidance to investigators and other research-active staff regarding internal processes, procedures, approval forms, SOPs.
    - Performed R&D feasibility trials to determine the product’s merit and viability using HPLC (High-Performance Liquid Chromatography) and UV for analytical validation.
    - Prepared and executed New Product Development Reports which helped in examining all the aspects of a proposed project including technical, economic, financial, legal and environmental conditions.
    - Prepared R&D trial reports, Batch Manufacturing Records and Validation Protocols following ALCOA principles.
    - Assisted in preparing and executing Product Development reports, preparation of Validation Protocols and quality assurance parameters using QMS software.
    - Ensured adequate checks on data quality, risk management parameters, root cause analysis and implementing CAPA during OOS events.
    - Expert in documentation and data maintenance, retrieving and analysis. Expertise in legal documentation and guidelines of MHRA, EMA.
  • Pharmacy Consultant (Feb, 2020–Jul, 2024) at Walgreens - Boots Alliance Company Ltd. London
    Managing patients and preparing patient's pharmacy records and analyzing complex data sets using pharmacy management tools.
    - Involved in Collecting, Interpreting, Analyzing, Dispensing, Retrieving and Handing Out of Prescriptions.
    - Provided support to the healthcare professionals and care home units regarding the patient data in accordance with the SOP of the organization.
    - Managing seasonal vaccination services from its booking, tracking, and record keeping using Statistical tools.
    - Experience in Stock management, exception counts, and resolving stock-related errors using pharmacy management tools.
    - Involved in internal audits.
    - Provided counseling to the patients.
    - Knowledge of regulatory requirements.

Education

  • M.Sc. in Pharmaceutical Sciences with Industrial Practice (Jan, 2020–Jan, 2022) from University of Greenwich, UK
  • B.Pharm (Sep, 2010–Aug, 2014) from Rajasthan University of Health Science

Fee details

    ₹2,000–5,000/hour (US$21.05–52.63/hour)

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