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QC Analyst

5651306

Stevenage, England

2 days ago

28706 - 38747 GBP

GSK

www.gsk.com

Brentford, United Kingdom

Emma Walmsley

$10+ billion (USD)

Company - Public

1830


Job Description

Site Name: UK - Hertfordshire - Stevenage
Posted Date: May 11 2023


CLOSING DATE:
25th May 2023

  • x2 positions are available across HPLC and Compendial testing.

GSK make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 2.3 billion packs of medicines and doses of vaccines in 2022.

We are addressing gender equality at all levels within our organisation, we also remain committed to improving ethnic diversity within GSK and recruiting and developing talent that mirrors the communities in which we work. With support from our Global Disability Council and our employee resource group, the Disability Confidence Network, we are working hard to create an inclusive workplace.

We want GSK to be somewhere everyone can feel a sense of belonging and thrive. Our success absolutely depends on our people.

As a QC Analyst you will be responsible for the routine testing of various samples for internally and externally manufactured Biopharm products. You will also be responsible for ensuring that analytical tests are successfully transferred, and method validation is performed where appropriate.

In this role you will…

  • Perform evaluation of samples submitted from both internal and external manufacturing sites, and test samples utilising a range of chemical, biochemical and biological tests while participating in the validation of test methods and equipment used.
  • Apply knowledge of Electrophoresis, HPLC, or Compendial testing to the provision of product testing and stability data while working with the line manager or designated analyst to interpret test results.
  • Maintain detailed laboratory records in accordance with current Good Manufacturing Practice (cGMP), ensuring that all records and test results are accurately prepared and checked, peer reviewed prior to submission for approval for authorisation.
  • Record deviations from the normal practice and out of specification results appropriately and report them to the line manager; assist with investigations product and test anomalies.
  • Deliver and assess formal training programmes for staff and trainees as required.
  • Write, review, and update Standard Operating Procedures (SOPs) and associated pro-forma used within the laboratory.

Why you?

Qualifications & Skills:

  • Understanding of cGMP compliance.
  • Knowledge of data review.
  • Good attention to detail.
  • Strong planning, organisational and problem-solving ability.
  • Able to communicate effectively across all levels of the business.

Preferred Qualifications & Skills:

  • Degree level education in science related discipline.
  • Understand the fundamentals of immunological assays.
  • Proficient in the use of corporate IT systems and software analysis packages.
  • Knowledge and understanding of biochemical techniques and analytical disciplines.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

As an Equal Opportunity Employer, we are open to all talent. In the US, we also adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, colour, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class*(*US only).

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Ukdiversity.recruitment@gsk.com or 0808 234 4391. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels

As you apply, we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit GSK’s Transparency Reporting For the Record site.


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