SigmaGraft Biomaterials, Inc is a biomedical device manufacturing company located in Fullerton, California.
We are looking for Research Associate/Scientist & Production Coordinator.
Web-Site : sigmagraft.com

Research Associate / Scientist

Job Summary

SigmaGraft Research Associate/Research Scientist will be an integral part of the R&D team.
Research Associate/Scientist will participate in ongoing and future research projects.
Current research projects are focused on developing biomaterials and medical devices for dental and orthopedic applications.

Key Responsibilities

– Performs routine scientific research tasks requiring the application of standard techniques, procedures, and criteria.
– Conduct experiments and research activities for optimization and development of new products
– Analysis of prototypes and samples at various stages of completion using bioanalytical techniques including SDS-PAGE, ELISA and colorimetric assays
– Makes detailed observations, analyzes data, and interpret results
– Designs, performs, and/or oversees experiments and data collection to ensure data integrity, quality control, and protocol compliance
– Adherence to good laboratory procedures and practices
– Performs miscellaneous job-related duties as assigned.

Preferred Qualifications:

– B.S. or M.S. in biochemistry, chemistry, or chemical engineering.
– Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.

Knowledge, Skills, Abilities Required:

– Ability to develop and follow research methodology and protocol.
– Knowledge of scientific approach and methodologies.
– Knowledge of scientific research principles, practices, and protocols.
– Ability to design, organize, and coordinate scientific research projects.

Production Coordinator

Job Summary
Production Coordinator will coordinate manufacturing; responsibilities will include effective planning, organization, and supervision of the manufacturing process
to maximize productivity. This position will assist in setting department goals/expectations.

Key Responsibilities
– Manage daily production activities such as output data, process data, etc.
– Facility management & equipment maintenance including IQ/OQ/PQ
– Improve productivity and safety by engineering efforts;
– Scale up of new product process from lab to commercial scale
– Experience in medical device industry and/or GMP condition is preferred
– Conduct department training to ensure compliance to procedure updates
– Lead meetings with direct reports and support groups in a professional manner
– Ensure compliance to regulations (FDS, OSHA, etc.)
– Partner effectively with Quality to monitor department quality and support corrective actions
– Set department goals/expectations and provide performance feedback to employees

Knowledge and Skills
– Bachelor degree in management or engineering
– Previous experience in the medical device industry or other highly regulated industry is preferred
– Must be a strong team player and process strong collaboration skills in partnering with cross functional stakeholders in order to achieve objectives
– Requires attention to detail and the ability to support big picture, strategic efforts
– Requires the ability to work and excel within a fast paced, dynamic, and constantly changing work environment
– Requires excellent communication skills (written and verbal), effective project management skills, and the ability to execute job duties with minimal supervision
– Knowledge of computer applications (i.e., Word, Excel, PowerPoint) a must

Benefits
– Health Insurance
– Paid Vacation & Holidays
– Sick Leave
– 401K

Working Hours : Mon-Fri 8:00AM – 5:00PM

Please send your resume to stevechang@sigmagraft.com