• Looking after DRAP (Ministry of Pakistan) matters.• Internal GMP Audits of my Pharmaceutical organization.• Responsible for Risk Management of Quality system.• Dossier preparation for Pharmaceutical generic medicine.• Pricing of Pharmaceutical products.• Trend analysis of market/Regulatory strategies.• Registration of Nutraceutical products. • Work on Health & Safety, Prepared their quality manuals, strategies, policies, sops and implementing within the organization. • eCTD dossier preparation/submission for pharmaceutical medicinal product in the ministry.

ATCO LaboratoriesSenior Regulatory Officer, December 2016 – July 2018Regulatory Officer, April 2015 – December 2016ACHIEVEMENTS:• Oversee registration of medicinal products, In the CIS region, ASEAN region, Sudan, Sri Lanka & Vietnam.• Maintain data integrity record of regulatory documents.• Conduct Bioequivalence Study from FDA approved CROs.• Conduct Comparative dissolution Profile study of different tablet dosage forms from different quality control labs.• eCTD dossier preparation/submission for a pharmaceutical medicinal product in the ministry RESPONSIBILITIES:Broad Functions: • To perform all aspects of regulatory affairs with a specific focus on EAC, CIS, and ASEAN territories.• To advise technical teams on contemporary regulatory requirements.• Handle the registration follow up with the distributors. • To collate and review relevant data for timely submission to regulatory authorities in accordance with export requirements. • To ensure that the company is at a high level of regulatory compliance through continual review of published information from relevant regulatory authorities. Principal Responsibilities: • Prepare and maintain regulatory submissions involving the collation, review, and assembly of scientific, medical, manufacturing, and other supporting documentation.• Liaise with regulatory agencies (Distributors) and internal departments to respond to Queries. • Coordinate with the technical department of new submissions, artwork, and review revisions to packaging artwork for compliance with approved labeling.

RESPONSIBILITIES:• To prepare CTD & ACTD/Annexure based dossiers for African and ASEAN countries. • Solve quarries related to dossiers.• Check & arrange drug manufacturer file. • Prepare case for “Certificate of Pharmaceutical Product” (Copp)• Monthly plan, agenda, and minutes of the meetings• Prepare list related to dossier dispatch, such as to Product to be applied, pending products, renewal of dossier registration, product obsolete in foreign ministry & list related to Registration timeline & Distributor.

• Analysis of sterile products (Water for Injection, Ampoules, Eye drops), • Dissolution Test, Disintegration Test, Hardness Test. • Assay test for Tablets, Capsules, Ointments & liquid products • Maintain Raw Data, Files for WFI • Reporting in SAP system Application products • Equipment handle and maintained • UV Spectrophotometer• Dissolution Apparatus • Tablet hardness tester • Disintegration Apparatus • LOD Apparatus o pH Meter• Conductivity Meter• Friabilator

Assess the status of the patient’s health problems and determine whether the prescribed medications are optimally meeting the patient’s needs and goals of care.Evaluate the appropriateness and effectiveness of the patient’s medications.Recognize untreated health problems that could be improved or resolved with appropriate medication therapy.Follow the patient’s progress to determine the effects of the patient’s medications on his or her health.Consult with the patient’s physicians and other health care providers in selecting the medication therapy that best meets the patient’s needs and contributes effectively to the overall therapy goals.Advise the patient on how to best take his or her medications.Support the health care team’s efforts to educate the patient on other important steps to improve or maintain health, such as exercise, diet, and preventive steps like immunization.Refer the patient to his or her physician or other health professionals to address specific health, wellness, or social services concerns as they arise.Provide a consistent process of patient care that ensures the appropriateness, effectiveness, and safety of the patient’s medication use.Consult with the patient’s physician(s) and other health care provider(s) to develop and implement a medication plan that can meet the overall goals of patient care established by the health care team.Apply specialized knowledge of the scientific and clinical use of medications, including medication action, dosing, adverse effects, and drug interactions, in performing their patient care activities in collaboration with other members of the health care team.Call on their clinical experience to solve health problems through the rational use of medications.Rely on their professional relationships with patients to tailor their advice to best meet individual patient needs and desires.

Pharmaceutical internships are the best way to bridge the gap between going to school and landing great job. Internships can help you develop your pharmaceutical industry experience by learning the ropes from more experienced professionals. At the end of your internship, you’ll have relevant experience to help you decide if a pharmaceutical career is the right choice for you.Under the supervision of a pharmacist, the pharmacy intern learns the basic operational skills required to be apharmacist. The pharmacy intern performs pharmacy-related functions in order to ensure the safe and effectiveness ofmedications within Zafa pharmaceutical.