Skip to main content
Post your CV and find your next job on Indeed!

Medical Records Summary jobs

Sort by: -
    • This role offers a clear path to develop your technical skills and take on increasing responsibilities while making a meaningful impact on patients' lives.
    • View all GlaxoSmithKline jobs - Barnard Castle jobs - Technologist jobs in Barnard Castle
    • Salary Search: Microbiological Technologist salaries in Barnard Castle
    • See popular questions & answers about GlaxoSmithKline
    • Reporting directly to the Medical Rostering Senior Manager you will have managerial responsibility for the management of medical workforce systems across the…
    • Conducts Source Document Review of appropriate site source documents and medical records.
    • Our Clinical Solutions team members act with a drug development…
    • Prepare source documentation and file study-related documents and medical records as required.
    • Basic knowledge of medical terminology.
    • Knowledge of medical terminology and emergency response protocols.
    • Assess patients' conditions and administer appropriate medical interventions.
    • Typically, you will be required to carry out a simple medical questionnaire, a physical examination (height, weight, blood pressure) and sample collection.
    • Experience in maintaining accurate records and following clinical protocols.
    • Annual individual performance review and maintaining records of personal and…
    • Maintain accurate patient records and documentation of all procedures.
    • Strong knowledge of anatomy, physiology, and medical terminology.
    • To design, deliver and develop digital training courses under the digital training portfolio to Trust staff, and other relevant internal and external stakeh…
    • Follow property specific procedures for handling emergency situations (e.g., evacuations, medical emergencies, natural disasters).
    • Role Purpose: To coordinate and oversee the delivery, monitoring, and reporting of social value activities across Spire Healthcare.
    • You will lead statistical planning and delivery across clinical programs and contribute to clinical developments plans within oncology.
    • Post-production review of Clinical or Commercial batch records.
    • Knowledge of regulatory requirements in pharmaceutical/medical device industry.
    • Conducts Source Document Review of appropriate site source documents and medical records.
    • Verifies required clinical data entered in the case report form (CRF)…
    • Prepare samples for laboratory processing, maintain clear records and communicate relevant information to colleagues.

People also searched:

medical assistant
medical devices
medical receptionist
medical sales
medical secretary
medical writer
records assistant
records officer
recorra

Job Post Details

GlaxoSmithKline logo
Microbiological Technologist
GlaxoSmithKline
·
4.1
Barnard Castle
Full-time
Apply on company site

Job details

Pay information not provided
Full-time
Barnard Castle

Full job description

Microbiological Technologist - Secondment / FTC until the end of 2027.

Closing Date: 5th November 2026 (COB)


Business Introduction
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.
Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.
We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary
Join us to play a vital role in ensuring the quality and safety of medicines through microbiological testing. You will work closely with manufacturing, quality, and technical teams to support our mission of uniting science, technology, and talent to get ahead of disease together. Our team values practical problem-solving, attention to detail, and a positive attitude. This role offers a clear path to develop your technical skills and take on increasing responsibilities while making a meaningful impact on patients' lives.

Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
  • Perform routine microbiological testing of raw materials, in-process samples, finished products, and environmental monitoring using approved methods.
  • Maintain, calibrate, and troubleshoot laboratory instruments and equipment to ensure data accuracy.
  • Record, analyse, and report microbiological results clearly and accurately using laboratory information systems.
  • Support investigations related to deviations, out-of-specification results, and non-conformances to identify root causes.
  • Assist in validation, transfer, and improvement of microbiological methods and procedures.

Why you?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
  • Bachelor’s degree or higher in Microbiology, Biology, Biomedical Science, or a related scientific discipline.
  • Practical experience in a regulated laboratory environment, including microbiological testing methods.
  • Knowledge of good manufacturing practice (GMP) and good laboratory practice (GLP).
  • Proficiency in using laboratory instruments, such as incubators, autoclaves, microscopes, and microbiological media preparation.
  • Ability to follow detailed procedures precisely and work independently when needed.
  • Strong communication skills and willingness to collaborate closely with diverse teams.

Preferred Qualification
If you have the following characteristics, it would be a plus:
  • Experience with sterility testing, bioburden, endotoxin testing, or environmental monitoring in pharmaceutical settings.
  • Familiarity with laboratory information management systems (LIMS) and electronic data capture tools.
  • Understanding of microbiological method validation and regulatory compliance standards.
  • Participation in laboratory investigations and root cause analysis.
  • Interest or experience in continuous improvement techniques such as Lean or Six Sigma.
  • Ability to contribute actively to cross-department projects or audits.

Work arrangement
This role is fully on-site in the United Kingdom at our Barnard Castle site. You will work alongside a collaborative team within the laboratory environment five days per week.

Ready to make a difference with your skills in microbiology? Apply now with your CV and a brief note on why this role excites you. We welcome applicants from all backgrounds and support reasonable adjustments throughout our recruitment process. Join us and help shape the future of healthcare.


Skills

Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations


Why GSK?

Uniting science, technology and talent to get ahead of disease together.


GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.


People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.


GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.


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 at UKRecruitment.Adjustments@gsk.com where you can also request a call.


Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive


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 the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Let Employers Find YouUpload Your Resume