Oligo/dna Technical Expert

3 weeks ago

Lancashire, United Kingdom Intertek Full time

**We need you to have**:

- Proven experience of one or more of the following analytical disciplines:
- LC-MS, including HRMS for elucidation of intact mass, sequencing, modifications, Capping efficiency, and Poly A tail distribution.
- NGS for sequencing.
- Chromatographic methods for assessment of product integrity and quality.
- Spectroscopic methods for assessment of melting temperature and gross structure.
- Potency assays.
- Molecular Biology Techniques such as qPCR and / or ddPCR
- Can recognise the positive and negative impacts of utilising particular methods with a view to providing the best solution to the Client. Ensuring that all processes are aligned to the needs of the Client and fit with the schedule of works.
- Strong experience of creating methods from end to end with mínimal support or guidance across multiple projects.

**ABOUT THE OPPORTUNITY**

Working alongside the Laboratory Management and Business Development teams, you will manage the technical content of proposals and ensure the scientific integrity of data as well as facilitate the progress of a project or study whilst liaising with key members both within the Laboratory and across the wider business, whilst maintaining a collaborative approach which provides solutions and not ‘blockers’ and is supportive in nature.
- Provide technical expertise within the DNA based medicine characterisation team incorporating oligonucleotides and/or RNA based material and responsible for design of study and the scientific integrity of multiple analytical projects undertaken by the laboratory.
- Provide strategic direction to ensure our services remain the best possible solutions for our clients within the biopharmaceutical industry.
- Lead on R&D activities within the team producing research material for publication and presentation at industry events.
- Author and/or critically review analytical project reports in a speedy and efficient manner regarding accurate interpretation of the data and compliance with the Analytical Project Plan
- Ensure that all Quality Management documentation is completed in a timely manner
- Assist the Laboratory Manager in establishing Development Training plans for all team members
- In conjunction with the Project Manager and Laboratory Manager plan and organise analytical workload for themselves and other members of staff for whom they provide supervision, based upon business priorities and specific project deliverables
- Carry out project team briefings at the start of each project to explain the context of the project, define the deliverables and explain any specific testing requirements
- Carry out Team De‑briefings (review) with team members at the end of each project to discuss best practice and learnings which could be applied to future projects
- Liaise with the Quality Group to advise of any atypical project timelines or requirements

**WHAT WE OFFER**

Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
- Competitive salary/benefits
- Development and career opportunities around the Globe
- Working in a highly motivated team and dynamic working environment

In this opportunity you’ll be joining our Chemical and pharma team, based at Intertek Pharmaceutical Services Manchester (IPSM), Blackley Manchester

Intertek operates a preferred supplier arrangement and we do not accept unsolicited approaches from agencies.

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