1 week ago
Job type: Contract
Hiring from: USA Only
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.
Prepare high-quality documentation for regulatory submissions focused on CMC and mainly writing Drug Master Files.
This is a 6-month contract with our client and may require periodic trips to the Midwest.
Qualified candidates must have:
- Minimum five years of demonstrated experience writing in the CMC field for small molecule drugs
- Advanced degrees are a plus
- Good communication skills are essential
All candidates must be legally eligible to work in the United States.
We are an equal opportunity employer. M/F/D/V
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Before you apply, please check if any restrictions apply in terms of time zone or country.
This job has a geo-restriction in place:USA Only.
Please mention that you come from Remotive when applying for this job.
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