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 continues to support a wide range of life-sciences clients and at present we are looking to expand our team again to ensure our services are at the highest level possible. In this newly created function, we are seeking a Compliance and Quality Assurance Consultant who can initially support one project linked to Product Complaint management on a full time basis. This role is too become a permanent member of our team and we are looking for candidates with the potential to learn and grow their skills across the QA area.
Responsibilities included:
Provide operational support to QA activities linked to the complaint process for one global life-sciences client
Such tasks may include supporting the returns processing, temperature excursion evaluation, alert handling etc.
Support and lead deviation management as and when directed
Support other QMS tasks for clients based within the EU
Work towards expanding your skills and aim at becoming a Responsible Person or Qualified person
Skills required
Must be educated to at least a BSc level or higher within a life-sciences discipline
At least 2-4 years’ experience already gained with Quality Assurance for a Pharmaceutical or Biological group (a must requirement)
Previous experience with complaint management linked to QA activities (GMP, GDP) would be highly preferred
Fluency in English
Can commence a new project immediately full time for one year or more
Excellent communication skills
#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.***
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
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