Hameed Faheem Pazhey Pattillath Email & Phone Number

Swords, Fingal, Ireland

• Assembled and tested products in line with company procedures and technical drawings, ensuring top-notch quality according to ISO 13485 and EU MDR.
• Maintained precise documentation using SAP ERP, upholding compliance standards and regulatory requirements.
• Collaborated with team members to consistently meet and exceed weekly production targets.
• Prioritized safety, ensuring a clean, organized workspace and properly maintained equipment.
• Assisted in inventory management, ensuring stock accuracy and smooth workflow.
• Mentored and trained fellow operators, contributing to a skilled, high-performing team.

Dundalk, County Louth, Ireland

• Ensured meticulous adherence to packaging procedures according to EU cGMP regulatory guidelines.
• Upheld rigorous standards of quality control following strict GDP and Data Integrity principles throughout the production process.
• Met productivity targets consistently while strictly adhering to machine settings.
• Maintained a hygienic and orderly work environment in full compliance with GMP regulations.
• Prioritised safety by wearing appropriate protective gear and promptly reporting any hazards.
• Remained up-to-date with training requirements and company procedures.

Dublin, County Dublin, Ireland

• Provided high-quality, holistic care to residents with dignity and respect.
• Addressed resident needs promptly and maintain positive relations with them and their families.
• Adhered to company policies, procedures, and regulatory guidelines.
• Demonstrated competence in assigned duties, ensuring resident well-being.
• Effectively communicated within the team and upheld professional standards.
• Attended training, remained flexible for different shifts/sites, and represented the company professionally.

Carlow, County Carlow, Ireland

Abu Dhabi, Abu Dhabi Emirate, United Arab Emirates

• Developed and managed regulatory documentation (technical files, labeling information) for Class IIA medical devices, ensuring compliance with EU MDR and ISO 13485.
• Partnered with cross-functional teams to develop and implement regulatory strategies for new product introductions.
• Prepared and project managed high-quality device registrations for approval by the USFDA, EU Competent Authorities and regional authorities (ESMA, DHA and MOHAP)
• Acted as the Regulatory Affairs subject matter expert.
• Worked closely with the Quality team in the areas of Vigilance, Post Market Surveillance, and PSURs.
• Monitored the progress of New Product Development, Renewal, and Re-Authorisation submissions.

Kannur, Kerala, India

• Collaborated with clinicians and researchers, actively involved in patient medication prescriptions.
• Completed clerkship rotations in various speciality departments, including Cardiology, Nephrology, Neurology, and Paediatrics.
• Monitored and reported adverse drug reactions (ADRs), conducted medication history interviews, and providedpatient counselling.
• Contributed to research paper writing and reviewing for publication.

Msc. In Pharmaceutical Regulatory Affairs, Pharmacy, 1:1

Clinical and Non Clinical Evaluation of Pharmaceutical Technologies (Pharmacology, CHMP, Product Manufacturing and Testing, Clinical.

Doctor Of Pharmacy - Pharmd, 2:1

Clinical Pharmacy and Pharmacotherapeutics Pharmacoeconomics and Pharmacoepidemiology Clinical Research Internship: Departments of.

High School

Activities and Societies: • Best Outgoing Student - Batch of 2014 • Headboy - Student Council 2014