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Production Specialist
Gmp
Posted on 2/1/2022
INACTIVE
Locations
Menlo Park, CA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Management
Requirements
  • Tuesday - Saturday; 6:30am- 3:00pm
  • Sunday - Thursday; 6:30am- 3:00pm
  • This role is onsite. You must be able to commute to Redwood City, CA
  • BS/MS in Chemistry or a relevant sciences field
  • 2+ years of pharmaceutical and/or industry experience in cGMP/cGLP a plus
  • Desire to work in a fast-paced, collaborative startup environment
  • Experience running HPLC and solid phase extraction workflows a plus
  • Strong commitment to quality
  • Demonstrates strong interpersonal and communication skills (both written and verbal)
  • Ability to work independently and as part of a team, to meet departmental goals
  • Self starter who is comfortable working with limited guidelines
  • Able to lift/move up to 25 pounds
  • Comfortable to sit and/or stand for extended periods (up to 4 hours)
Responsibilities
  • 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
  • Follow established SOPs and revise SOPs, as necessary to ensure compliance
  • Properly record, analyze, and maintain batch records and supporting data per good documentation practices
  • Execute batch production records or protocols independently, efficiently, and in compliance with site and quality management system requirements
  • Collaborate with Supply Chain, Quality Assurance, Warehouse, and other cross-functional teams to meet deadlines
  • Practice continuous improvement by contributing ideas and suggestions to new and existing processes
  • Operate complex robotic high-throughput systems to manage products through a highly automated workflow
  • Organize, stock, and maintain work area to 5S and safety standards
  • Capture production data in compliance with site and quality management system requirements
  • Identify, communicate, and escalate processing or quality related issues
  • Ability to author documents such as protocols, change control records, deviation, master production records and SOPs
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