Quality Control Microbiology Manager

Posted 13 Hours Ago
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Redmond, WA
92K-131K Annually
Senior level
Biotech • Pharmaceutical
The Role
The Quality Control Microbiology Manager oversees the QC Microbiology lab operations in support of GMP manufacturing, including testing, mentoring staff, ensuring regulatory compliance, and collaborating with teams for continuous improvement. Responsibilities include managing lab functions, training, and establishing performance metrics.
Summary Generated by Built In

Just is seeking a highly motivated individual who desires a significant opportunity to improve worldwide access to biotherapeutics. We are looking for someone to join a fast paced, collaborative, and multidisciplinary team. This individual will join the Quality Control management team supporting the GMP manufacturing facilities in Redmond, WA and Seattle, WA. As the QC Microbiology Manger, you will be responsible for the daily oversight for the QC Microbiology lab operations in support of routine GMP operations, method transfer, validation and method lifecycle activities at Just-Evotec. The ideal candidate will have commercial GMP experience, will possess exceptional leadership skills and be a mentor to our science-based microbiology team.  Responsibilities will include in-process and drug substance sample testing, training of laboratory staff, GMP document authoring / revision, providing oversight in support of GMP operations and spearheading initiatives to build infrastructure and processes across both Washington state facilities. The ideal candidate has a keen attention to detail, is highly organized in their work and strong written and verbal communication skills.

Responsibilities:

  • Provide hands-on leadership for the QC Microbiology lab operations; management of daily/weekly/monthly activities of staff and operational oversight of group, data review, schedule, and training.
  • Oversee multiple QC analysts and direct management of individuals, including goal setting, performance feedback, skills development, and mentoring.
  • Lead and provide guidance for QC Microbiology testing and method qualification in support of GMP Biologics manufacturing, including in-process, stability, drug substance and drug product release testing by techniques such as bioburden, endotoxin testing, growth promotion, Gram staining, biological indicators, TOC, conductivity, microbial identification and plate reading.
  • Provide microbial SME support for microbial investigations and microbiological/aseptic related challenges.
  • Collaborate with Contamination Control Team by providing Environmental and Utility monitoring data and supporting investigations, trend analysis and report generation.
  • Manage all aspects of the Microbiology labs including the ordering supplies and maintaining laboratory equipment and lab spaces.
  • Support client audit/inspection readiness plans and interact with regulatory agencies during inspections on Microbiology/Environmental Monitoring related matters.
  • Establish and publish Key Performance Indicators (KPI) to track cGMP compliance for QC Microbiology. Capture metric information for use in continuous improvement of areas of responsibility.
  • Participate in daily and weekly operation meetings and Quality Management Reviews.

Requirements:

  • BS in Microbiology, Biology, Biochemistry, or related field with 5+ years relevant Quality experience and 10+ years’ experience in industry, including a minimum of 3+ years of hands-on, industry experience managing a cGMP QC Analytical or Microbiology laboratory.
  • Direct leadership experience preferred.
  • Expert understanding of cGMP's, FDA, USP, NSF regulations and ISO 14644 and USP/EU compendia methods
  • Audit and/or regulatory inspection experience
  • Experience deploying and working with electronic systems preferred.
  • Attention to detail and highly organized.
  • Proficient at technical writing including microbiological methods, technical summary reports and Standard Operating Procedures

Physical Requirements:

  • Travel between Seattle and Redmond site required.
  • Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet, and body.

This job description is intended to describe the general content of the job, and to identify the essential functions of and requirements for the performance of this job.  It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Because job requirements evolve with the changing needs of Just-Evotec Biologics business, this description is subject to change and may be modified at any time, whether formally or informally.

The base pay range for this position at commencement of employment is expected to be $91,560 to $130,800;  Base salary offered may vary depending on individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits.

Evotec (US) Inc. is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

Top Skills

Microbiology
The Company
HQ: Hamburg
5,042 Employees
On-site Workplace

What We Do

Evotec is a biotechnology company that is committed to advancing drug discovery and development. Through flexible business models, we collaborate with pharmaceutical companies, biotechs, foundations, and government agencies on a substantial scale. We believe that by working together, we can make a difference in the lives of patients.

Our Pipeline Co-Creation model represents our adaptable, multi-modality, fully integrated end-to-end approach to drive collaborations and services across all phases of drug discovery and development – from discovery of novel targets to achieving Proof of Concept in the clinic and into commercial manufacturing.

We aspire to contribute data-driven disease understanding and early disease relevance in humans to bring the probability of success up. We select the right modality, which is then propelled forward on our platforms by our passionate people striving for the fastest and most effective ways towards patient impact. This is enabled by convergence of human ingenuity with data and AI.

We also offer specific solutions, products, and CRO/CDMO-like services, always in support of the Biopharma R&D innovator. Our more than 4,000 scientists work closely with numerous partners concurrently, delivering fully integrated research and development portfolios or individual projects with the highest quality standards and efficiency, coupled with great science, passion, engagement, and communication.

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