Mohammed Tayab

I am a dedicated and dynamic Quality Assurance professional with over 6 years of experience in the pharmaceutical industry, covering clinical trials, laboratory operations, production, and quality control. My career has been marked by a strong foundation in GMP compliance, regulatory standards, and process improvement, contributing significantly to industry leaders such as Labcorp, Fortrea, and Mac Plc.

In my current role as a GMP QC Inspector at Mac Plc, I have been instrumental in defining and implementing stringent product quality standards, collaborating with production teams to achieve performance targets, and maintaining rigorous testing protocols to ensure compliance. A notable achievement includes playing a key role in securing the MIA License for our site by ensuring full compliance and readiness for inspection. I work closely with the Qualified Person (QP) to review and approve batches before release, ensuring that all products meet the highest regulatory and quality standards.

I have a proven track record of working effectively with sponsors to ensure the successful completion of large-scale projects. My ability to keep sponsors informed and confident in our work has been crucial to building and maintaining strong professional relationships. I take a forward-thinking approach, proactively identifying risks early in the process. Utilizing tools such as Failure Modes and Effects Analysis (FMEA) and Critical Control Analysis (CCA), I help to identify and mitigate potential risks, ensuring project success and safeguarding the interests of all stakeholders.

My expertise extends to managing Environmental Monitoring (EM) trends, handling CAPAs, change controls, and Out-of-Specification (OOS) investigations. I am also experienced in conducting batch releases, implementing Batch Manufacturing Records (BMRs), leading complaint investigations, and maintaining Standard Operating Procedures (SOPs). Additionally, I support the QA department in hosting internal and external audits, vendor evaluations, and deviation management.

I bring strong communication and negotiation skills, excellent problem-solving and decision-making abilities, and meticulous attention to detail. My effective time management skills and ability to work both independently and as part of a team ensure efficient project and team management. My qualifications, including certifications in COSHH writing and assessment, radiation protection supervision, and good manufacturing practice, underscore my commitment to safety and compliance within the pharmaceutical environment.

With extensive knowledge of UK & EU GMP, GCP, and broad experience in clinical trials, I am well-positioned to be a valuable asset to any quality assurance team. My proactive approach to identifying and controlling risks, along with my ability to liaise effectively with stakeholders such as Medical Directors, Principal Investigators, sponsors, vendors, and customers, ensures smooth operations and adherence to regulatory standards.

Driven by a commitment to excellence, I thrive in dynamic environments and adapt seamlessly to evolving challenges in the pharmaceutical landscape. I am eager to leverage my expertise to contribute to your team’s success, while continuously advancing my skills and knowledge in the field of quality assurance.

GMP QC Inspector, MAC Plc, August 2023 to present 

Bachelor of Sceince in Biomedical Science from the University of Bradford