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.
The role
We are currently working with a global Life-sciences brand as they are looking for additional support within their manufacturing Operations based in the Netherlands. At present we are currently looking for independent freelancers/contractors to work with our client for at least 6 months on a full time basis (1.0 FTE). This role offers Hybrid working with at least 3 days required onsite in Leiden throughout the duration of the project and it is to commence immediately.
Essential Functions Include
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Support the continuous improvement efforts within a GMP setting
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Can support and lead team members on performing CAPA’s and deviations
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Ensure these processes are correctly managed and timelines achieved
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Support other Quality Operational tasks as and when needed
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Work successfully across the QA team and provide key support for the continuous improvement mindset
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Overall support and coaching of colleagues within the GMP
Experience required
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Ideally further educated to BSc or higher within a life-sciences discipline or an applicable area
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Must have demonstrated exposure to working within a GMP setting within the Biological area (ATMP, CGT etc.)
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Can demonstrate key skills in QA GMP
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Fluent in English
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Can work on Hybrid basis in Leiden
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Can perform the project to the desired requirements set out in the Job description
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.***
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
