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Production Supervisor
Gmp
Confirmed live in the last 24 hours
Locations
Menlo Park, CA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Management
Marketing
Research
Requirements
  • This role is onsite. You must be able to commute to Redwood City, CA
  • 2+ years experience managing a production laboratory operation
  • Experience with oligonucleotide synthesis, running HPLC purification or solid phase extraction workflows a plus
  • Strong understanding of laboratory best practices, continuous improvement methodologies, and lean manufacturing principles, including 5S, Gemba, and Kaizen
  • Experience with formal quality management systems required, ISO 13485 and cGMP preferred
  • Innovative, motivated, and independent leader possessing a player/coach mentality
  • “Big picture” thinking and adaptability with ability to navigate challenges and concerns to finding the best path forward
  • Excellent interpersonal and organizational skills
Responsibilities
  • Manage, mentor, and develop a growing team of research associates responsible for the production of GMP sgRNA products and services
  • Responsible for end-to-end oligonucleotide manufacturing including reagent preparation, equipment set-up, synthesis and post-processing (cleavage and deprotection, purification, and lyophilization) of GMP sgRNA products
  • Design and implement standardized laboratory management and maintenance protocols leveraging lean manufacturing methodologies
  • Collaborate with Supply chain, Quality Assurance, Warehouse, and other cross-functional teams to meet project deadlines and scheduling timelines
  • Collaborate with science, engineering, and marketing teams to design and implement innovative solutions to meet and exceed customer expectations
  • Coordinate with Quality, Process engineering and supply chain to ensure the seamless transfer of new products and processes into production
  • Uphold strict production and quality control processes to ensure incoming, in-process, and finished goods materials meet all published specifications
  • Participate in the site audit program, ensuring compliance to all published procedures
  • Ability to author documents such as protocols, change control records, deviation, master production records and SOPs
  • Ensure lab standards are upheld, labware and equipment are properly maintained, and hazardous materials are disposed of in accordance with regulatory requirements
Synthego

201-500 employees

Next-gen genome engineering
Company Overview
Synthego’s mission is to enable agile life science research and development from discovery through clinical introduction by providing scientists unprecedented access to advanced genome engineering products at high throughput.
Benefits
  • Generous Equity Package
  • Medical, Dental & Vision
  • 401(k) Plan
  • Catered to You
  • Fully Stocked
  • Transportation
  • Green Environment
  • Stay Fit
  • Legal Ease