Job Description

Job Introduction

QA Document Controller

Liverpool



Pharmaron is a global CRO helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 sites across the UK, US and China, and we support drug discovery through to manufacturing with fully integrated, high-quality services.


We're proud of the impact we make--just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules to gene therapies, and we work with more than 3,000 global customers.


We're seeking a proactive and detail-oriented QA Document Controller to join our QA Team in our Liverpool to ensure the integrity of documentation, document control and systems to maintain GMP standards

At Pharmaron we offer:

Vibrant and dynamic employment - we are a highly specialised, growth company operating in a critical sector of the economy - our future is strong and exciting! Opportunities to develop your skills and yourself - our rapid growth brings greater opportunities for you to learn and grow faster! A great team where we all support each other - enjoy your work - after all, you spend about a third of your time here!

Key roles and responsibilities:

Provide document creation support Ensure formatting complies. Generation and management of document control procedures and templates Creation and generation of documentation. Control and issue of document and logbook numbers Logbook reviews Maintain secure and readily retrievable master document files Archive management. Provide support during regulatory inspections. Maintain and manage TWD electronic document management system Provide training and coaching to site Raise QMS as required to support the document control system Provide KPIs for management review. Support site activities to provide documents in a timely manner

Requirements:

GCSE levels or equivalent in Maths and English Experience in a GMP document control system role MS Word skills Good knowledge of IT systems Effective organisational and time management skills Excellent attention to detail and a methodical approach Customer service focused Ability to work autonomously and in a team Attention to detail, works to high level of accuracy

Our Company:

"We are a dynamic, fast-growing company, with an enviable reputation for leading-edge science, offering contract research services to some of the world's leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges."


We are based in the vibrant city of Liverpool with a world-class R&D and manufacturing facility that offers a complete end-to-end development service. Our 80,000 sq. ft facility houses an established Biologics Department that consists of Analytical and Process Sciences. Our Liverpool site has a remarkable 20-year track record in Biologics Development, now offering a fully integrated gene therapy drug substance solution in our state-of-the-art cGMP facility purpose-designed for viral vectors with onsite plasmid DNA and renowned analytical capabilities for release and characterisation.

We offer a competitive salary and a progressive and comprehensive suite of employee benefits. We offer a state-of-the-art working environment in our modern Liverpool site. We offer the opportunity for growth and development and will support funding for relevant training and development programmes.


We do more than manufacture batches, we develop medicines!

Why Should You Apply?

This is an opportunity for you as a science professional to make a real impact in a highly scientific and regulated environment, demonstrate ambition and the desire to grow with the department. Build and shape your career in an environment that sets and commits to the highest standards. Be part of a team who support each other, embrace and solve technical challenges, and put excellence at the heart of all that we do.


Pharmaron is a premier R&D service company supporting the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities having established diverse drug R&D service capabilities, ranging from synthetic, medicinal, and analytical chemistry, biology, DMPK, pharmacology, drug safety assessment, radiochemistry and isotopically labelled metabolism, chemical & pharmaceutical development to clinical development. With operations in China, US