Quality Assurance Specialist

Posted 18 Hours Ago
Be an Early Applicant
Redwood City, CA
105K-115K Annually
1-3 Years Experience
Biotech
The Role
The Quality Assurance Specialist is responsible for overseeing deviations, complaints, and corrective actions while ensuring compliance with ISO 9001:2015 and FDA regulations. The role involves investigating root causes, conducting risk assessments, and managing quality system programs to drive continuous improvement in the quality management system.
Summary Generated by Built In

This position is responsible for oversight of all Deviations, Non-conformances, Customer Complaints and Corrective/Preventive Actions at Synthego. The ideal candidate will be responsible for improving the current processes and bringing in new systems for process improvement as a part of the Quality Assurance team. 

What You'll Do:

  • Continues to build on professional concepts toward culture of quality in compliance with ISO 9001:2015 standards and FDA regulations 
  • Trend Quality indicators and lead continuous improvement of QMS. 
  • Establish and oversee key quality system programs including, Corrective and Preventive Actions, Deviations, Non-Conformances and Customer Complaints for all different product lines.
  • Proactively investigates root cause of deviations (planned and unplanned); may work independently or cross-functionally across the organization to troubleshoot and provide resolution. 
  • Conducts risk assessments of failures and makes recommendations for problem resolution and prevention, in accordance with compliance requirements
  •  Participates in product development or improvement initiatives, ensuring internal and regulatory compliance 
  • Responsible for reviewing and managing applicable Standard Operating Procedures (SOPs) and Work Instructions (WI) related to continuous improvement

About You:

  • Bachelor’s degree in Science (Chemistry, Biochemistry, Microbiology) or Engineering 
  • 2+ years in Quality Assurance; or experience working in a cGMP regulated environment with positions of progressive responsibility. 
  • Experience executing process improvement or overseeing CAPA processes in a cGMP environment 
  • Expertise in Standard Operating Procedures, Good Manufacturing Practices: ISO 9001 
  • Overall understanding of Quality Assurance specifications and process 
  • Ability to communicate and work cross functionally with other teams. 
  • Ability to influence in a team environment and collaborate with peers. 
  • Performance focused, persistent, sound decision-making, open minded, innovative/creative and results oriented. 
  • Ability to work effectively on problems of diverse scope, with analysis/evaluation of data. 
  • High level of personal motivation and initiative, and ability to work independently on projects. Attention to detail, safety, quality and customer requirements. 
  • Proficiency with MS Office and GSuite products. 

Company Perks & Benefits:

  • Equity options 
  • Medical, dental, and vision benefits
  • 401k Program
  • Catered meals on Tuesday and Thursday
  • Paid parental leave
  • Flexible paid time off

About Us

 

Synthego is a genome engineering company that enables the acceleration of life science research and development in the pursuit of improved human health.


Based on a foundation of engineering and chemistry, Synthego leverages automation and machine learning to synthesize high-quality CRISPR reagents for science at scale. Synthego’s mission is to enable agile life science research and development from discovery through clinical trials by providing scientists with comprehensive CRISPR solutions for each phase coupled with full technical and regulatory support from industry-leading experts.


With its technologies cited in hundreds of peer-reviewed publications and utilized by thousands of commercial and academic researchers and therapeutic drug developers, Synthego is at the forefront of innovation, enabling the next generation of medicines by delivering genome editing at an unprecedented scale.

The Company
HQ: Menlo Park, CA
443 Employees
On-site Workplace
Year Founded: 2012

What We Do

Synthego is a genome engineering company enabling the acceleration of life science research and development in the pursuit of improved human health.

The company leverages machine learning, automation, and gene editing to build platforms for science at scale. By vertically integrating hardware, software, bioinformatics, chemistry, and molecular biology, Synthego is at the forefront of innovation advancing the next generation of medicines through providing access to genome editing at an unprecedented scale.

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Our Culture of Diversity: Different Faces from Different Places

At Synthego, our differences make us unique, help us innovate, and allow us to persevere. We stand firmly behind our values, strive to achieve representation, and celebrate diversity in perspectives and backgrounds. We welcome all team members to be their best selves as we move forward towards fulfilling our shared vision of revolutionizing genome engineering technology to help make biological therapies accessible to all patients.

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