Director, Production and Quality Management (110-229) Synthetic Genomics
THIS JOB HAS EXPIRED
Job Description
The Director of Production and Quality Management is responsible for implementing and managing the procedures for production, data management and quality assurance. Specifically, the professional is responsible for developing and executing the company?s manufacturing, process control and quality management system to meet industry standards, company goals and customer requirements.
Required Skills
Work as part of the management team to translate the business goals into production and quality goals
Understand industry best practices in terms of production management and quality control procedures and systems and identify best practices for company
Establish budget and requirements and infra-structure required to support operations and quality assurance
Design and develop conceptual process designs covering production and quality control steps
Lead the implementation and management of production and operational protocols for DNA and RNA synthesis
Implement and manage best in class production, data management and quality control operations
Ensure compliance with all laboratory procedures, including GXP?s (cGMP, GMP, GLP), quality and safety policies and best practices
Ensure seamless data security and management throughout the production workflow
Manage priorities and production orders to create production schedules and meet turnaround requirements
Ensure seamless integration with front-end (order entry), back-end (shipping, invoicing, customer service) and suppliers process
Create, implement, evaluate the company?s production management policies, standards, procedures and plans
Review supplier performance
Develop and maintain QA and performance standards and tracking systems
Participate in customer, supplier and internal meetings
Manage PMS and QMS to develop reporting procedures
Lead production and quality management communications
Oversee internal audit
Ensure compliance with all laws, regulations and required certifications
Required Experience
Requires a Masters or Ph.D. in Engineering, Molecular Biology or related field
At least 10 years relevant experience in production or quality management
Requires a knowledge of DNA sequencing and synthesis processes
Track record managing biotechnology products production and quality assurance
Experience establishing and implementing production, quality management, performance and cost protocols, and manufacturing management systems
Well versed with regulatory standards and experience implementing cGMP standards and protocols
Must have team-oriented management experience and leadership ability, including supervision of scientists
Highly-motivated, innovative professional with critical thinking, organizational and problem-solving skills to independently design, execute, troubleshoot and interpret experiments
Excellent communication and interpersonal skills to effectively participate in a multidisciplinary team
Job Location
La Jolla, California, United States
Position Type
Full-Time/Regular
| Location: |
La Jolla, CA
United States
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THIS JOB HAS EXPIRED