GxP Technical Administrator

at 30Technology

Who we are

30 Technology was created as a group of eight wholly owned subsidiaries aligned to its research programs and market verticals: 30Respiratory, 30Woundcare, 30Therapeutics, 30Pharma, 30Dermatology, 30AnimalHealth, 30Innovation and 30TB.

30 Technology aims to unlock and deliver the promise of therapeutic nitric oxide by developing and defining new models of care to treat many serious medical conditions by enhancing the body’s healing and defence mechanisms. Nitric oxide (NO) is a volatile gas, produced in tissues of the body, which acts as a vital cellto-cell signalling mechanism.

The discovery NO is involved in a number of critical physiological processes led to a 1998 Nobel Prize. Since then, a number of attempts have been made to harness its multiple therapeutic effects which include increased blood flow, regulation of immune response, abroad-spectrum anti-microbial activity and acceleration of healing.

However, NO has a very short half-life, so sustained release and practical delivery is difficult to attain. 30 Technology has solved these previously intractable problems, utilizing proprietary IP to create a platform technology which uniquely creates the opportunity to use NO in a variety of diseases and health conditions.

Additionally, our revolutionary 30TechnologyTM Intellectual Property allows us to deliver sustained NO into the lung via aerosol, through the skin via topical patches, gels, liquids and into the body for release from biomaterials in regenerative medicine. Our technology is clinically proven and a potent solution to many serious medical conditions.

To achieve its goals, 30 Technology has been highly successful in its first round of funding, raising more than £30m.

30 Technology is an equal opportunity employer. All applicants will be considered for employment without attention to race, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

About the role

  • Sector: Technology
  • Contract type: Permanent
  • Salary: Based on experience and qualifications
  • Application Closing Date: 31st December 2020

Our ideal candidate will have

As a GxP Technical Administrator at 30 Technology, your responsibilities will be to manage cross-departmental administrative activities that facilitate the smooth running of Regulatory/Quality Assurance (QA) and Technical Operations laboratory associated processes; you will oversee and maintain databases, collate data, draft regulatory documents, work closely with the quality team and work with vendors and contractors.

You'll ensure that laboratory equipment is procured by supporting the Head of Technical Operations, tracked, maintained including its GxP validation status, and that documentation is complete, accurate and filed.

You will oversee the administrative management of the Quality Management System (QMS) under the guidance of the Head of Quality Assurance to ensure the health of the QMS. This will include ensuring all controlled documents are available, up to date and tracked, issued, trained on and retired, management and quality control (QC) of training records and required training.

You will also be involved in assisting all teams including senior management, as needed for any structural and/or ancillary tasks as well as carrying out basic laboratory techniques and methodologies after appropriate training.

Working at the very heart of the 30 Technology teams, your role will involve daily liaising with all functional team members and having to juggle multiple tasks at a time.

You will be highly organised and have the attitude that ‘no task is too small’ when carrying out office, QA and lab administrative/regulatory duties. This office-based role will be at our Milton Park site, Abingdon. Working from Home can be considered once the role has been established and is functioning successfully.

• Liaise with vendors to procure quotes and purchasing laboratory equipment, consumables and supplies
• Keeping records of lab expenditure, equipment validation status, assisting with validation activities
• Set up and maintain scientific databases, including data management, tracking of documentation and data and its associated filing
• Oversee metrology logs to ensure annual PM/PQ of equipment is carried out in a timely manner
• Draft and review quality documents to support laboratory equipment and method validations
• Be able to process and interpret large data sets
• Manage administrative activities for the Quality Management System including maintaining the effective controlled documents list, management of deviation and CAPA logs, follow up with staff to ensure in time document updates, management of training files and assist in the management of training including QC of records on a quarterly basis
• Being able to “muck in”/help out with whatever is needed to keep the laboratory and office running smoothly!

Essential Requirements
• A minimum of BSc degree Biological Sciences, Chemistry or equivalent
• Having worked in a regulatory environment will be a great advantage – GCP, GLP, GMP experience
• Excellent organisational and time-management skills
• Strong IT skills and knowledge of Microsoft Office Suite (Word, PowerPoint, Excel)
• A knowledge of Computer System Validation is advantageous
• The ability to prioritise tasks, work under pressure and with minimum supervision
• Excellent interpersonal, oral and written communication skills
• Strong attention to detail
• A problem-solving approach to work

Desired - But Not Essential Experience
• Be familiar with basic scientific systems and processes

To be considered for this exciting opportunity, please submit your CV and a cover letter to Dr M Sajid (mohammed.sajid@30.technology) or Karen Hue (karen.hue@30.technology).

Disclaimer: Please note that job vacancies which are displayed on this website are only from companies based at Milton Park. The job description, recruitment process and subsequent employment offers are managed by and are the sole responsibility of the hiring company and are in no way connected to MEPC.

How to apply

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