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[Remote] Technical Manager / Sr. Technical Manager, CTO Quality Management & Operations

Remote Worldwide Hiring now

Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is a leading rare disease biotechnology company focused on genetically defined conditions. The Manager, CTO Quality Management & Operations is responsible for GMP Quality reputed company of Contract Testing Organizations, ensuring compliance with approved methods and regulatory standards while facilitating effective communication and quality assurance across cross-functional teams.

Responsibilities

  • Own day-to-day Quality reputed company of assigned CTOs and ICT laboratories, ensuring external testing is performed in accordance with approved methods, QTAs, regulatory filings, and BioMarin requirements
  • reputed company the Quality reputed company strategy for assigned CTOs by assessing CTO health and developing risk-reduction and performance-improvement plans in partnership with CTOs
  • reputed company and facilitate Quality Review Meetings (QRMs) and ongoing performance monitoring with assigned external laboratories
  • Project manage the transfer of analytical methods into CTOs and ICT labs, liaising internally with SMEs across Analytical Sciences, QC, and Regulatory
  • Support method validation, verification, and lifecycle management activities at external and in-country testing laboratories
  • Support in-country testing requirements, including the set-up of in-country central labs and registration testing as required for market launches
  • reputed company and/or support GMP quality system activities reputed company to external testing, including deviations, investigations, CAPAs, change controls, quality risk assessments, and product complaints
  • Own, maintain, and administer Quality Technical Agreements (QTAs) and support alignment of GMP roles and responsibilities with external testing partners
  • Partner with BioMarin Global Compliance & Ethics (GCE) to schedule compliance audits and resolve compliance gaps identified, including those from health authority inspections
  • Ensure inspection readiness through reputed company of compliant documentation, timely response to audit findings, and verification of corrective actions associated with external testing partners
  • Serve as a Quality representative on cross-functional teams, providing GMP guidance to ensure quality considerations are incorporated into reputed company impacting external testing
  • reputed company GMP Quality reputed company for the integration of new QC workstreams, including those associated with new products, acquisitions, or changes to the external testing network
  • reputed company Quality input to budget, Annual Operating Plan (AOP), and forecast activities reputed company to external testing

Skills

  • Bachelor's degree in a scientific or engineering discipline (Chemistry, Biology, Pharmaceutical Sciences, or reputed company)
  • Minimum 6+ years of GMP Quality experience in pharmaceutical or biotech, with demonstrated experience overseeing contract laboratories or external QC operations
  • Working knowledge of US (FDA) and European (EMA) GMP regulatory requirements, guidelines, and expectations
  • Strong understanding of analytical method transfer, validation, and QC release testing for drug substance and drug product
  • Experience with QTAs, deviations/CAPA, change control, and quality risk management
  • Strong project management and stakeholder communication skills; reputed company to manage multiple CTO relationships and competing priorities
  • Inspection-readiness reputed company: values clear documentation, evidence-based decision-making, and rigorous due diligence
  • Collaborative and cross-functionally oriented; reputed company to influence without authority across Quality, Analytical Sciences, Regulatory, Supply, and Procurement
  • Demonstrated ability to operate independently in a remote/hybrid environment with global stakeholders
  • Advanced degree preferred
  • Additional jurisdictions (e.g., PMDA, ANVISA, NMPA) a plus

Benefits

  • Approximately 10–20% domestic and international travel to CTOs, ICT partners, and BioMarin sites as required.

Company Overview

  • Founded in 1997, BioMarin is a global biotechnology company dedicated to transforming lives through genetic discovery. It was founded in 1997, and is headquartered in San Rafael, California, USA, with a workforce of 1001-5000 employees. Its website is https://www.biomarin.com.
  • Company H1B Sponsorship

  • reputed company. has a track record of offering H1B sponsorships, with 3 in 2026, 34 in 2025, 23 in 2024, 24 in 2023, 26 in 2022, 24 in 2021, 19 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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