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Freelance Consultant Product Lifecycle Management- nitrosamines

Job Work from home
Posted 24 Mar 2024
Work experience
3 to 5 years
Full-time / part-time
Full-time
Job function
Degree level
Required languages
English (Fluent)
Dutch (Fluent)

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ProPharma Group is an industry leading, single source provider for regulatory compliance, pharmacovigilance, and medical information services across the full development lifecycle for pharmaceutical, biotechnology, and medical device companies. Operating around the world with offices in Australia, Canada, Germany, Japan, the Netherlands, Sweden, United Kingdom, and the United States, ProPharma Group’s fully integrated service offerings will provide clients with a comprehensive suite of global support services that are required to be competitive in today’s dynamic markets. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes.

Job Description

The Consultant will support a variety of projects at our clients. Your responsibilities include setting up or participating in tech transfer projects and support of manufacturing processes, monitoring timing and costs and progress reporting on deliverables. The consultant will execute these tasks based on his/her expertise in this field. He/she immerses into the client's complete problem, analyses short term as well as long term needs and makes relevant proposals. A consultant recognizes (un)spoken wishes and complaints, develops solutions and takes action to extend service to the client.

Due to an increase in projects, we are currently looking for freelance consultants who can support our clients in a number of nitrosamines projects.The assignment will be assessing and reviewing possible structural reactions in drug product compositions that can lead to toxic byproduct(s). These assessments will be taken on a bigger risk assessment about forming possible impurities that are harmful to patients that take the aforementioned drug products on a daily basis.

This is a freelance remote-based project.

Qualifications

Qualified candidates must have:

  • An academic degree in organic chemistry
  • 3 - 5 years experience in tech transfer and/or manufacturing of (bio)pharmaceutical products
  • Experience in GxP regulations
  • Knowledge of product-related validations
  • Able to asses a multiple information and filter out relevant molecular structural details
  • Report in a pre-agreed fashion within a template
  • Excellent communication skills (oral and written) in English
  • Analytical skills, proactive, decisive, listening skills, flexible and negotiation skills
  • Enthusiastic & self-starter

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

Pharmaceutical
Leiden
Active in 10 countries
89 employees
30% men - 70% women
Average age is 42 years