Cedent Consulting
MAJOR DUTIES AND RESPONSIBILITIES
Responsibilities will include, but are not limited to:
- Initiate, direct, and execute all scientific research and/or development strategies in research and/or development.
- Investigate the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products, and problems.
- Plan and execute laboratory research for your own work while aiding others as needed.
- Maintain broad knowledge of state-of-the-art principles and theories.
- Provide support to junior team members with knowledge and guidance for analytical test results, investigations, and analytical team activities.
- Develop, establish, and validate testing methodology used to control raw materials, production intermediates, and final products (new or existing).
- Establish, validate, and document new or existing compound methods.
- Conduct work and review of work in compliance with cGMP, safety, and regulatory requirements.
- Author research reports, stability reports, test protocols, and test reports while aiding others as needed.
- May participate in development of patent applications.
- Support company goals and objectives, policies and procedures, ISO/MDD/MDR/FDA/ICH requirements, the Quality System Regulation, and other regulatory requirements.
- Perform other duties as assigned as needed, collaborating with other functions.
QUALIFICATIONS
Experience:
- Minimum 10 years of relevant, hands-on experience in the medical device/pharmaceutical/Biotechnology industry.
- Team player with an energy level and drive that motivates and guides those around them to persevere through tough situations and ultimately to meet agreed-upon goals.
- Cross-functional collaboration experience in order to support overall company goals.
- Good oral and written communication skills.
- Basic computer skills.
EDUCATION REQUIREMENTS
- Bachelors degree in science or equivalent relevant experience.