Position: Mid-Senior level

Job type: Contract

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Job content

Job Introduction

We are looking for:

To support independent monitoring of compliance with identified Standards and procedures and the administration of the compliance systems.

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:

Under the supervision of the Line Manager:

  • Support the internal audit programme to assess compliance with the identified Standards and SOPs according to the schedule set by the Quality Assurance Manager.
  • Consult on making recommendations for change, to drive a culture of continuous improvement.
  • Support document control activities in the document control system, to include requests for new document creation and provide compliance review of controlled documents.
  • Support activities in the Corrective and Preventive Actions (CAPA) Database.
  • Support activities in the Change and Improvement (C&I) Database.
  • Support the successful running and continued certification of the Management Systems.
  • Support client due diligence, supplier, and 3 rd party audits.
  • Ensure that any operating practice which may affect compliance is brought to attention of the Quality Assurance Manager.
  • Work efficiently such that work is carried out in a well-planned, organised way and in a timely manner.
Requirements:

  • Good attention to detail
  • Good IT skills with working knowledge of MS Office
  • Good organization, written and verbal communication skills
  • Good interpersonal, influencing and negotiation skills
  • Knowledge of working in a scientific field
  • Methodical and thorough approach to work
  • Good time management skills and ability to work to tight deadlines
  • Able to communicate effectively at all levels within a large organisation
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 believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.

The Cardiff site is Pharmaron’s global centre of excellence for the custom chemical synthesis of drug and complex chemical substances radiolabelled with tritium or carbon-14, offering radiolabelled custom synthesis service to clients in the pharmaceutical, agrochemical and industrial sectors. We offer our employees a supportive teamwork environment, enabling them to develop and liberate their true potential.

  • We offer a competitive salary and a progressive and comprehensive suite of employee benefits.
  • We offer state of the art working environment on site.
  • We offer the opportunity for growth and development and will support funding for relevant training and development programmes.
Why Should You Apply?

  • This is an opportunity for you as a Quality Assurance professional to make a real impact in a highly scientific and regulated environment, demonstrate leadership, 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.
  • To 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 and UK staffed by over 19,000 employees, Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan, and China.
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Deadline: 25-06-2024

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