GenScript/ProBio

GenScript/ProBio

Manager of Quality Assurance

Redmond, Washington, United States

Sponsorship not specified$100k-$120kDetected 1 day ago
NegotiationSupply ChainMolecular BiologyLeadershipCommunication

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odds of building a lasting career here

50Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds (Level II)66
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~30% per draw at Level II). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

Personalize to your clock →

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About the role

  • The position reports to the Senior Vice President of the Innovation Center and is responsible for the strategic development and operational management of the site's ISO 9001-certified Quality Management System (QMS).
  • GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce.
  • Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources.

Responsibilities

  • demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
  • GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.

Requirements

  • Master's degree in a life sciences-related field (or equivalent) with 5+ years of QA/QC experience in a biotech production environment, including substantial management responsibility.
  • Experience with molecular biology product manufacturing (oligonucleotides, synthetic gene, mRNA) or formulation services is highly desirable.
  • Expert knowledge of quality risk assessment, CAPA management, and change control methodologies within an RUO or ISO-certified manufacturing environment.
  • Proven track record in establishing or optimizing a quality organization and working collaboratively with R&D, production, and QC groups.
  • Completed Lead Auditor training or possesses deep working knowledge of ISO 9001:2015 standards.
  • Extensive experience hosting external customer audits and filling out supplier quality questionnaires in a B2B life sciences or CRDMO environment.
  • Experience drafting and negotiating Quality Agreements with clients, with a strong ability to manage customer expectations appropriately for an RUO setting.
  • Excellent diplomacy, negotiation, and customer-service skills, with the ability to confidently explain and defend quality systems to technical and quality representatives from partner organizations.
  • Strong interpersonal, verbal, and written communication skills.
  • Benefit:
  • Medical Insurance/ Vision Insurance/ Dental Insurance
  • 401(k) & Retirement Savings Plan (RSP)
  • Short Term Disability Insurance
  • New Child Leave

Compensation

  • $100,000 - $120,000 total compensation, including bonus, depending on experience and qualifications.

Benefits

  • Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one.
  • We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays.
  • We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs

Equal opportunity

  • equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce.

Visa & Work Authorization

  • ity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protecte
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This listing is sourced directly from GenScript/ProBio's careers page and normalized into a canonical job model.