QC Scientific Officer
Thermo Fisher Scientific, Inc.
Swindon,United Kingdom
6d ago

Job Description

When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and be part of a team that values performance, quality and innovation.

As part of a successful, growing global organization you will be encouraged to perform at your best. With revenues of more than $20 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.

At our site in Swindon, ThermoFisher are forging partnerships that are transforming the industry, creating new business models between pharma companies and their pharma service providers.

We are pioneering solutions that are driven by client needs, with successful recent partnerships including Flexion and Pacira.

We currently offer solutions spanning the entire pharmaceutical life cycle to help pharma and biotech companies of all sizes meet their complex development and manufacturing needs at any stage or scale enabling us to deliver a combination of unrivaled quality, reliability and compliance, backed by a reputation for scientific and technical excellence.

The range of services at ThermoFisher for drug substances and drug products is wider than that of any other CDMO and we offer end-

to-end capabilities and expertise to take your discovery from pre-clinical and clinical development, through scale-up, all the way to commercial supply across more than 40 oral solid, sterile and softgel dosage forms.

Key Accountabilities

  • To transfer methodology into the business, to perform routine laboratory procedures, and to perform project work within the department.
  • To carry out projects within the Department and at international level, as required.
  • To prepare technical documentation within the Department, as required.
  • To assist in the development and validation of laboratory procedures within the team, as required.
  • To train others as required.
  • To review analytical and laboratory data within the Department for accuracy, completeness and compliance with documented procedures.
  • To communicate effectively with others on site and internationally, and to participate with them in problem solving activities, as required.
  • To assist in the development and validation of laboratory procedures within the team and with other organisations internationally, as required.
  • This includes but is not limited to purchase & qualification of equipment.

  • Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business.
  • To carry out any other tasks which may be required from time to time
  • Experience

    You will be a flexible, highly motivated and experienced quality professional seeking a new opportunity to develop and grow your skills within a unique operating model.

    To be considered for this role you will have experience of the Pharmaceutical industry and a strong understanding of current GMP and technical processes.

    In addition to this we are looking for an individual who is able to demonstrate

  • Degree in Chemistry or strongly related scientific discipline
  • Experience of instrumental and traditional analytical techniques.
  • Ability to work to critical time lines with the ability to commit to overseas travel as part of the project team.
  • Effective communication skills at all internal and external levels.
  • Excellent attention to detail.
  • Excellent organisational skills
  • When applying for this role, please use the 'cover letter' of the on-line application to describe how you meet the competencies for this role, as outlined in the job requirements above.

    The information that you have provided in your cover letter and CV will be used to assess your application.

    Thank you for your interest in this opportunity.

    Add to favorites
    Remove from favorites
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Application form