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 group. 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 will be based in Leiden throughout the assignment and ideally will commence in September 24.
Essential Functions Include:
Key support to various GMP manufacturing activities across the site which could include validation activities with equipment; supporting technology transfers; production support and training; process qualification and validation tasks as well as other areas such as operational readiness
Work closely with other key departments to support ongoing activities in QA for example
Provide ongoing support to the service group and help provide troubleshooting activities; CAPA and deviation management
Provide training where necessary
Support with other activities when directed
Experience required
Ideally further educated to BSc or higher within a life-sciences discipline or applicable area
Must have demonstrated exposure to working within the life-sciences sector within a GMP setting
Can provide direct experience to support a number of tasks described within the job description (Support tech transfers, QA activities etc.)
Fluency in English
Can work onsite in Leiden
Strong communication & stakeholder 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.***