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. 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.
ProPharma are currently looking to partner with a new Freelance/Contract QA Consultant to support our ongoing Quality Assurance efforts in Sweden. Ideally we are looking to collaborate with an independent Consultant to support us on various projects for 8 hours per week over the course of 6-12 months. This project can be performed remotely from Sweden; it is to commence in June and we pay hourly for the support. The role will be a mixture of GMP/GDP related tasks so being an Responsible Person at present with GMP skills would be preferred but demonstrated experience in both is still acceptable without RP exposure.
Essential responsibilities will include:
Support a variety of GDP/GMP tasks across a range of projects as designated by ProPharma.
Such activities may include supporting audits; CAPA’s; support RP’s with compliance efforts etc.
Provide SME support when required to GMP/GDP activities
Use continuous improvement methods to enhance the quality system of our clients/ProPharma
Overall support for QA activities as requested via ProPharma
Qualifications required
Educated to at least a BSc level or more within a life-science or related discipline (engineering backgrounds would also work with sufficient experience)
Must have demonstrated experience in at least QA GMP related tasks with GDP exposure being highly preferred also
Fluency in English is a must
Currently based in Sweden and can perform the project as set out in the job description
Excellent communication skills and meeting deadlines efficiently
#LI-DNI
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.***
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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
