Utilize your scientific understanding, detail-orientation and organization to:
- Develop and support the company processes and efforts in the management and organization of
all scientific documentation, reports, and findings from the Research and Development
- Create, implement, maintain and manage documentation systems consistent with Regulatory
Affairs & Quality guidelines and R&D needs.
- Manage documents through the change control process including editing, proofreading,
tracking, distributing, and archiving.
- Work closely with the VP Regulatory Affairs and Quality in all aspects of the documentation
control strategy and implementation.
Minimum BS degree in the life sciences or affiliated area with solid experience in the
pharmaceutical industry, together related work experience. Unmatched organizational and detail
orientation. Prefer minimum 1.5 years of focused Document Control experience.
Earlier stage industry experience is helpful, together with a solid working knowledge of how
fast growing drug development companies are managed. Further, it is important to clearly
articulate complex concepts and ideas to your peers and throughout the organization. The
successful candidates will have excellent interpersonal skills and be effective working in a
collegial team environment.
Compensation and Benefits:
We offer an excellent remuneration package.
Please e-mail your resume/cv with your name, job title and code 'DCTRL-MNSTR-9-05' in the
subject line to: firstname.lastname@example.org , Please attach your resume as a Word document. EOE,
Diversity Focused, and Drug Free Workplace Employer.