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Genezen

Viral-vector and cell-therapy CDMO provider

Manager/Senior Manager - Quality Control, Microbiology

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLexington, MA, USA$130k - $170kIn-person

About the Job

Requirements

  • A Bachelor of Science degree in Microbiology, Biology, or a related scientific discipline is essential.
  • At least 8 years of GMP Quality Control experience, including at least 4 years of management experience.
  • Advanced knowledge of global GMP guidelines, especially United States and European Union guidelines, is essential.
  • Strong leadership in team management, decision making, change management, collaboration, delivering desired business results, and the ability to influence.
  • Ability to prioritize and operate with a sense of urgency.
  • Solid organizational, analytical, and problem-solving skills.
  • Effective communication skills and the ability to interact with stakeholders at all levels, with demonstrated interpersonal skills.
  • Demonstrated ability to solve problems and implement practical solutions in a dynamic and innovative environment.
  • Strong operational and business acumen.
  • High integrity and commitment to ethics and compliance standards.
  • Openness and transparency in sharing data and information.
  • Adaptability to changes in work schedule based on business needs.
  • Ability to meet the stated physical demands, including sitting for long periods; frequently standing, sitting, using hands to handle objects, reaching, and lifting or moving up to 10 pounds; occasionally walking, climbing or balancing, stooping, kneeling, crouching, crawling, and lifting or moving up to 25 pounds.
  • Must pass a criminal background check and drug screen.
  • Must be eligible to work in the United States; the employer does not sponsor visas.

Responsibilities

  • Maintain a safe, efficient, functional, and compliant laboratory operation in accordance with GMP standard operating procedures, guidelines, and regulations.
  • Coordinate day-to-day management of Quality Control Microbiology operations, including high-level planning of activities and resources, guidance and performance reviews within Quality Control, and cross-functional communication.
  • Manage and develop direct reports by setting clear goals, providing performance feedback, supporting career development, and recognizing and rewarding exceptional performance.
  • Oversee testing of in-process samples, drug substance and drug product release and stability samples, and complaint samples.
  • Oversee environmental and utility monitoring according to standard operating procedures, sample test requests, approved protocols, and investigations.
  • Maintain data integrity to the highest industry standards.
  • Oversee timely investigation of out-of-specification, out-of-trend, and other laboratory exceptions; manage deviations, change controls, and corrective and preventive actions; and maintain critical reagents, controls, and laboratory supplies.
  • Manage outsourced testing activities as necessary and ensure results are reported in a timely and compliant manner.
  • Develop, maintain, and continuously improve Quality Control systems for sample management, testing, data approval, data management, data archiving, and validation and calibration of Quality Control equipment.
  • Participate in cross-functional continuous improvement projects that support site improvements and cost efficiency.
  • Support and participate in internal and external inspections and audits, including regulatory inspections.
  • Collaborate with Quality Control Technical Services on method validation, specification generation, stability studies, and lifecycle management of methods, reference standards, and critical reagents.
  • Support new equipment validation and implementation.
  • Provide Quality Control data internally and actively support and participate in cross-functional teams, including CMC, Quality Management, Management Review Meetings, and SRB.
  • Escalate issues promptly to Quality senior management and cross-functional support teams.

About the Company

Genezen

Viral-vector and cell-therapy CDMO provider

Genezen is a contract development and manufacturing organization (CDMO) focused on gene and cell therapies, specializing in viral vectors and transduced cells. It provides end-to-end, fee-for-service development and cGMP manufacturing, from early development through clinical-grade vector production for trials. The company differentiates itself by offering a global, single-partner solution that covers the entire viral vector and cell-therapy pipeline. Its goal is to help clients advance gene and cell therapy programs by delivering reliable development, manufacturing, and testing support toward clinical trials.

Company size
201-500
Company stage
Growth Equity (Venture Capital)
Total funding
$18.5M
Headquarters
Lexington, MA
Founded
2014

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