Quality Manager (M-Th 4pm-3am / 4/10's)

Posted 5 Days Ago
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Pensacola, FL, USA
In-Office
Senior level
Biotech
The Role
The Quality Manager leads night shift quality operations, ensuring compliance with regulations and QMS while overseeing investigations, coaching teams, and driving process improvements.
Summary Generated by Built In

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva, you will be able to continuously improve yourself and us – working on challenges that truly matter with people who care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.

Learn about the Danaher Business System, which makes everything possible.

As the Quality Manager (Night Shift) provides site-level quality leadership during off-shift manufacturing operations. This role ensures compliance to QMS, regulatory, and customer requirements while supporting uninterrupted operations, real-time issue resolution, and strong quality culture across night shift teams.

This position reports to the Sr Manager Site Quality, that leads Quality on nights, located in Pensacola, Florida. This is an on-site role.  At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

What you will do:

  • Serve as the primary quality authority for night shift, providing real-time decision making and escalation as required
  • Ensure consistent application of QMS, DBS/lean principles, and site procedures during night shift activities
  • Oversee night‑shift investigations, ensure evidence‑based RCA, and escalate systemic issues to site quality leadership
  • Lead containment, risk assessment, and disposition decisions for deviations, nonconformances, batch documentation, and material holds during off‑shift operations.
  • Coach night‑shift teams on quality ownership, standard work, and DBS problem solving; identify trends and drive improvements that prevent recurrence

Who you are:

  • Hold a Bachelor’s degree, preferably in Science, Business, or Engineering.
  • Have at least 5 years of experience in Quality Assurance, Quality Engineering, or Manufacturing Operations within Life Sciences, Biotechnology, Medical Device, Biopharma, or other FDA/EPA-regulated manufacturing environments.
  • Possess an additional 2 years of leadership experience, in Operations, Quality Engineering within a regulated industry.
  • Leadership and Communication: Proven ability to lead, coach, and mentor teams; manage performance; plan succession; and effectively communicate at all organizational levels, both written and verbal.
  • Willing to go to Gemba

Travel, Motor Vehicle Record & Physical/Environment Requirements:

  • Ability to travel 10% of the time to other Cytiva manufacturing locations in the US and Worldwide, as required.
  • Ability to access gauges and equipment 5-6 feet off the ground, lift and move 20-35 lb. parcels.
It Would Be a Plus If You Also Possess Previous Experience In
  • Contamination control, sterilization, sanitation, or E-beam processes, including ISO 14644 cleanroom operations.
  • Enterprise systems such as SAP, Oracle, Veeva, or Magic, supporting laboratory or quality operations.

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

This job is also eligible for bonus/incentive pay. 

 

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. 

 

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law. 

 

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or [email protected].

Skills Required

  • Bachelor's degree in Science, Business, or Engineering
  • 5 years of experience in Quality Assurance, Quality Engineering, or Manufacturing Operations
  • 2 years of leadership experience in a regulated industry
  • Proven ability to lead, coach, and mentor teams
  • Willingness to travel 10% of the time

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

Cepheid Insights

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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