Description
LGMPharma is a leading contract development and manufacturing organization (CDMO)and provider of Active Pharmaceutical Ingredients (API). With excellent APIsourcing and supply chain expertise together with our drug product contract development and manufacturing solutions, LGM is a premier end-to-end solutions provider to the global pharmaceutical industry.
We are a high-growth organization looking to accelerate the development and commercialization of high-quality therapeutics worldwide. We have offices in California, Texas, Kentucky, Florida and Israel and are searching for a Pharmaceutical Technical Writer in Colorado Springs, CO.
RESPONSIBILITIES:
- Edits and writes Pharmaceutical Development and R&D Quality system policy, procedure, work instructions and other supporting documents
- Drafts CMC sections of regulatory filings, manage submission projects and keep supporting documentation files organized and up to date
- Interacts with Formulation and Analytical Development SMEs in R&D to support and/or write documents/reports/laboratory instructions that are accurate and usable
- Works with Regulatory Groups in managing their regulatory submissions
- Manages and supports the document development, maintenance and change request process for multiple documents simultaneously
- Analyzes documents and document sets to identify opportunities for improvement
- Manages multiple, sometimes conflicting priorities
- Other responsibilities as assigned
QUALIFICATIONS: Bachelor of Science degree in a Life or Physical Science
- 5+ years related experience, or equivalent combination of education and experience; or
- Master of Science degree in a life or physical science plus publication and at least 1 year laboratory experience also considered
- Excellent verbal and proven written communication skills
- Able to handle multiple high priority documents/projects simultaneously
- Able to interact effectively at various levels within the organization, with our customers and other external contacts
- Working knowledge of CMC sections in Module 3 sections of regulatory filings and eCTD (electronic common technical document)
- Fluent in MS Office and familiar with CMC documentation in the CTD format
- Able to quickly learn complex business processes and specialized terminology
- Able to work both independently and collaboratively with little supervision
- Able to work in a changing environment with changing priorities
