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Application Scientist job in Oxford at Manpower

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Application Scientist at Manpower

Application Scientist

Manpower Didcot, Oxfordshire, Oxfordshire Full-Time
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Manpower are currently recruiting for a project owner, who has experience with pharmaceutical QA/QC and with pharmaceutical customers.

Location: Harwell, Didcot

*20% of this role is travel based, you will be expected to engage with pharmaceutical customers via visits.

Shift pattern: Monday to Friday, 9am until 5pm.

Start date: ASAP

Contract length: 1 year.

Job Description

We are looking for a project owner to join our clients global marketing team in Molecular Spectroscopy.

The successful candidate will be working with a team focusing on developing a total solution to add value in pharmaceutical cleaning verification using FTIR. You will work with pharmaceutical manufacturing customers, introducing cutting edge technologies with an intent to define future opportunities. You will be reporting to the Head of Pharmaceutical Business for Molecular Spectroscopy and expected to travel up to 20% of the time.

In summary we are looking for an experienced, self-driven professional with pharmaceutical QA/QC experience for pharmaceutical customers to improve their manufacturing workflow.

Responsibilities includes but not limited:

Work with a project team to introduce a new way of instantly determining cleaning verification with IR surface analysis for pharmaceutical manufacturing using an existing instrument
Work with key pharmaceutical opinion leaders in developing applications workflows, and knowledge of best practice for this new way of working
Support commercial team with sales & marketing material for existing solution in current cleaning verification market
Work with a project team to determine customer requirements, barriers to entry, route to wider market, etc. and business case for next generation instrument to identify opportunities of further improvements and solutionsQualifications

Experience working within pharmaceutical quality or manufacturing environment and knowledge of pharmaceutical manufacturing workflow is key
Experience in achieving data integrity, compliance of instruments and computer systems validation requirements in GMP regulated environments
Experience in analytical method development in pharmaceutical QC laboratories
A good understanding of analytical instrument techniques
Clear writing skills to be able to communicate scientific ideas succinctly to develop sales materials, e.g. app notes, SOPs
Project management skills with the ability to influence cross functional team to operate in a collaborative environment
Excellent problem-solving skills with attention to detail; ability to step back and analyse the overall business impact

Recommended Skills

Product Quality Assurance
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Job ID: 213498098


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