For the past 20 years, ProPharma 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. As the world’s largest RCO (Research Consulting Organization), ProPharma 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 & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
At present we are currently supporting a life-sciences client as they now are now looking for interim support for an exciting R&D venture within the Biological arena. In this function, we are looking for an ‘Downstream Scientist – Process Development’ to work on an extended project for at least one year on a full time basis (1.0 FTE). This project will be based in Stockholm onsite and the project will ideally commence on 1st January.
Responsibilities include
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Develop and optimise Downstream processes for Biological products
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Ensure all process development work is completed within Regulatory requirements
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Provide technical and scientific support relating to a number of aspects including tech transfers, manufacturing process, troubleshooting etc.
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Work successfully on a cross-functional basis and manage external partners when required
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Write SOP’s, protocols and other relevant technical documents
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Support Regulatory submission activities
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Overall support to DSP activities and other process development areas where required
Qualifications
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Must be educated to at least a Bachelors or higher within a life-sciences discipline
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Must be able to demonstrate key experience in Downstream process development for Biological products (a must)
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Fluency in English
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Must be able to demonstrate hands-on skills in development of DSP production processes
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Can perform the project as designated within the job description
Strong stakeholder management skills
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.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Top Skills
What We Do
ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies.
With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science
