Senior Pharmacy Technician

IQVIA; Manchester; On-site; GBP 32,000 - 42,000; Full time

Job summary

IQVIA is seeking a Senior Pharmacy Technician for the Medicines Evaluation Unit (MEU) in Manchester. You will oversee the manufacture, preparation and assembly of IMP and ensure equipment is maintained and compliant with GPhC, MHRA, GMP and GDP.

You will prepare study paperwork and support protocol reviews to ensure accuracy and patient safety. The role requires communication skills, GMP experience and a pharmacy background, with opportunities for professional development within a global

Qualifications

• Bachelor's degree in Pharmacy or equivalent
• GPhC registered technician is desirable
• Experience in GMP regulated environments preferred
• 1 year experience in a Pharmacy environment
• Computer skills: Word, Excel, PowerPoint; good English communication

Responsibilities

• Oversee manufacture, preparation and assembly of IMP
• Manage maintenance, calibration and lifecycle of pharmacy equipment
• Prepare and review study paperwork (drug dispensing forms, material specs)
• Review protocols for IMP and pharmacy requirements
• Assist with IMP preparation under manufacturing licence and documentation
• Conduct independent verification of post-QP dose preparation activities
• Check dose calculations, product selection, preparation records, labelling and accountability for study protocols

Skills

Attention to detail

Written and verbal communication

GMP experience

Pharmacy experience

Education

Bachelor's Degree in Pharmacy

GPhC registered technician

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Senior Pharmacy Technician Medicines Evaluation Unit (MEU) This role is office based in Manchester. The Medicines Evaluation Unit (MEU) Ltd, an IQVIA business, is one of the UK’s leading contract research organisations, and a facility where commitment to excellence is paramount. Possessing extensive pharmaceutical, scientific and clinical expertise, allied with fast volunteer recruitment, both healthy and patient, within a state-of-the-art hospital based research facility, enables the MEU to offer clients positive clinical trial solutions. Join us on our exciting journey!

Job Overview

To assist and oversee the manufacture, preparation and assembly of IMP. Responsible for the oversight, maintenance, qualification, calibration, and lifecycle management of all pharmacy equipment to ensure compliance with GPhC, MHRA, GMP, GDP, and relevant regulatory requirements. This includes coordinating routine servicing and preventive maintenance, maintaining equipment inventories and records, ensuring equipment remains fit for purpose. Preparation and review of study related paperwork e.g. drug dispensing forms, material specification forms. Review protocols and provide input with respect to IMP and Pharmacy requirements. Assist with preparation of IMP under the manufacturing licence including the completion of all associated documentation. Responsible for undertaking or overseeing the independent verification and review of all post-QP dose preparation activities to ensure accuracy, compliance, and patient safety. This includes the independent checking of dose calculations, product selection, preparation records, labelling, accountability documentation, and dispensing activities in accordance with study protocols.

Requirements

Bachelor's Degree in Pharmacy (desirable). GPhC registered technician (desirable) Experience within a GMP regulated environment. Attention to detail. 1 year experience within a Pharmacy environment. Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint. Written and verbal communication skills including good command of English language.

Join IQVIA to see where your skills can take you High level of autonomy. Global exposure Variety of therapeutic areas Collaborative and supportive team environment Access to cutting-edge and innovative, in-house technology Excellent career development and progression opportunities Work-Life Balance, with a strong focus on a positive well-being. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.