MAJOR DUTIES AND RESPONSIBILITIES Responsibilities will include, but not be 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
Bachelor’s degree in science or equivalent relevant experience
San Lorenzo, California