Company Description
Welcome to Amicus, a CGMP consulting firm based in Columbia, SC. We provide consulting services to the pharmaceutical, biotechnology, and medical device industries, helping companies navigate the complexities of CGMP regulations to maintain compliance and optimize manufacturing efficiency. Our team of seasoned industry experts offers holistic, customized solutions that align with our clients' business objectives. We focus on fostering sustainable growth and competitive edge by ensuring quality, safety, and efficacy in manufacturing processes.
Role Description
This is a contract or full-time role for a Pharmaceutical Project Manager at Amicus for immediate placement with established clients. The Pharmaceutical PM will be responsible for developing and management detailed project timelines, allocated project resources, and issues which arise through execution (personnel and financial). The role requires experience working in a pharmaceutical GMP environment with knowledge of GMP validation and qualification requirements and approaches. Persons applying for this position should be able to manage multiple complex products simultaneously while coordinating meets and discussion between Amicus team consultants and clients.
Qualifications
- Knowledge of Good Manufacturing Practice (GMP)
- Experience in equipment and/or computer system validation/qualification processes
- Strong analytical and problem-solving skills
- Strong technical writing ability
- Excellent written and verbal communication skills
- Bachelor's degree in Engineering or a related field
- Certification in Project Management
- Experience utilizing project management tools (SmartSheet, Jira, ZOHO, etc.)
- 2 - 3 years experience in the pharmaceutical, biotechnology, or medical device industries