At a Glance
- Tasks: Design and manage analytical strategies for innovative therapeutic programmes.
- Company: ProPharma, a leader in biotech and pharmaceutical consulting.
- Benefits: Flexible remote work, competitive pay, and a commitment to diversity and inclusion.
- Other info: Collaborative environment with opportunities for personal and professional growth.
- Why this job: Join a dynamic team making a real impact in healthcare advancements.
- Qualifications: PhD or MSc with extensive experience in analytical development.
The predicted salary is between 60000 - 80000 £ per year.
For the past 25 years, Pro Pharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Pro Pharma partners with its clients through an advise-build-operate model across the complete product lifecycle.
With deep domain expertise in regulatory sciences, clinical research solutions, quality it can offer work up to 1.0FTE but with some flexibility and it will run for 6 months initially with an extension very likely.
It can be performed remote based anywhere within the UK and EU and ideally we would be looking to partner with independent consultants.
Key responsibilities Design, implement and manage the analytical strategy for a pegylated enzyme therapeutic program.
Work across the team as an SME to provide key guidance across the project Lead and support SEC-HPMC method development and validation for Phase 3 registration activities Assess analytical risks and develop mitigation strategies to support program objectives.
Key participation within project/scientific teams and offer sound advice/guidance on analytical development strategies Overall support the client as and when directed Skills required Ideally educated to a Ph D level in a scientific discipline or at least a MSc with substantial experience linked to the project Must have a proven SME level in analytical development in the above area Hands on experience of SEC-HPLC method development is a must at Phase 3 10-15 years experience overall working in the industry (more would also be suitable) Proven track record in supporting unlicensed medicines through troubleshooting phases to FDA registration Fluent in English Can perform the project as set out in the above job description Additional information We celebrate our differences and strive to create a workplace where each person can be their authentic self.
We are committed to diversity, equity, and inclusion.
Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits.
With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at Pro Pharma are personally reviewed by a member of our recruitment team.
We do not rely on AI screening tools to support our hiring process.
You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
Whilst Pro Pharma supports remote working, we also recognise the value that comes from in person collaboration.
As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager.
All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. ***Pro Pharma Group does not accept unsolicited resumes from recruiters/third parties.
Please, no phone calls or emails to anyone regarding this posting.***
