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Evening Quality Assurance Biotech Jobs (NOW HIRING)

PSC Biotech

Validation QA Specialist

Pomona, CA · On-site

$110 - $120/hr

At PSC Biotech ® , it's about more than just a job--it's about your career and your future. Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Chamblee, GA · On-site

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Alpharetta, GA

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Chamblee, GA

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

CorDx

Quality Assurance Manager

Alpharetta, GA · On-site

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

Cellular Technology Limited (CTL)

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Quality Assurance Specialist

Shaker Heights, OH · On-site

$55K - $70K/yr

... a global biotechnology company with locations and distributors worldwide. We are the industry ... As the Quality Assurance Specialist, you will support and contribute to the Quality Management ...

Integrity Consulting

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Quality Assurance Inspector

Santa Ana, CA · On-site

$20 - $24/hr

Seeking a QA Inspector familiar with the biosciences field who can check incoming and outgoing ... or biotech environment. · Computer skills including Microsoft Word, Excel, and Outlook PREFERRED ...

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Evening Quality Assurance Biotech information

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How much do evening quality assurance biotech jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for evening quality assurance biotech in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What is an evening quality assurance biotech?

Evening Quality Assurance Biotech jobs involve ensuring that biotechnology products and processes meet quality standards during evening or overnight shifts. Professionals in this role perform inspections, review documentation, run tests, and monitor compliance with regulatory guidelines, often in a laboratory or manufacturing setting. They play a critical role in maintaining product safety and efficacy, troubleshooting issues, and supporting continuous improvement efforts. Evening shifts help maintain around-the-clock quality oversight, which is essential for companies that operate 24/7.

What skills and qualifications are needed to thrive as an evening quality assurance biotech?

To excel as an Evening Quality Assurance Biotech, you need a solid background in biological sciences, quality control protocols, and typically a bachelor's degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and quality assurance certification such as ASQ is often required. Strong attention to detail, analytical thinking, and effective communication are vital soft skills for identifying and resolving compliance issues during evening shifts. These competencies ensure product safety, regulatory compliance, and continuous improvement in biotech manufacturing environments.

What are typical challenges faced by evening quality assurance biotech professionals, and how can they be addressed?

Evening Quality Assurance (QA) professionals in biotech often encounter challenges such as limited access to daytime resources, time-sensitive batch releases, and effective communication with cross-functional teams who may work different shifts. To overcome these, it's important to establish clear documentation practices, utilize digital communication tools for shift handovers, and proactively coordinate with production and laboratory staff. Staying organized and maintaining a strong attention to detail are critical, as QA decisions directly impact product quality and regulatory compliance.

What is the difference between Evening Quality Assurance Biotech vs Evening Quality Control Biotech?

AspectEvening Quality Assurance BiotechEvening Quality Control Biotech
Primary FocusEnsuring compliance, reviewing documentation, and process auditsTesting products, analyzing samples, and verifying quality
CertificationsGMP, ISO, QA-specific trainingGMP, ISO, Lab certifications
Work EnvironmentOffice and production oversight, documentation reviewLaboratories, testing facilities
Common TasksAudit preparation, SOP review, compliance checksSample testing, data analysis, report generation

While both roles support biotech quality, Evening Quality Assurance Biotech focuses on compliance and documentation, whereas Evening Quality Control Biotech emphasizes product testing and sample analysis. Understanding these differences helps candidates choose the role that best matches their skills and career goals.

What cities are hiring for Evening Quality Assurance Biotech jobs?

Cities with the most Evening Quality Assurance Biotech job openings:

What are the most commonly searched types of Quality Assurance Biotech jobs?

The most popular types of Quality Assurance Biotech jobs are:

What states have the most Evening Quality Assurance Biotech jobs?

States with the most job openings for Evening Quality Assurance Biotech jobs include:

Evening Quality Assurance Biotech jobs near you

Quality Assurance Associate

Krystal Biotech

Pittsburgh, PA • On-site

Full-time

Re-posted 24 days ago

Job description

About Krystal Bio:
At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Job Description Summary:
Krystal Biotech, Inc. is seeking a highly motivated and experienced Quality Associate to support quality systems, GMP manufacturing processes and documentation practices at our headquarters in Pittsburgh's South Side.
Primary Responsibilities:
  • Work with internal teams to obtain an understanding of the product and the documentation requirements.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended use.
  • Develop expertise on FDA regulations and audit processes.
  • Initiate and update GMP manufacturing associated documentation, such as clearing procedures.
  • Provide oversight of daily QA functions which include review and approval of records generated by manufacturing and quality control documents.
  • Provide support for updates on standard operating procedures and associated forms.
  • Assist with QA efforts for site cGXP documentation related to the operation of gene therapy manufacturing.
  • Ensure compliance with regulatory agencies and oversee continuous improvement of company's QA and compliance functions.
Requirements & Desired Competencies:
  • Minimum of a Bachelor's Degree (Biology or related Life Science) with 3+ years of relevant quality systems experience in the biotech or pharmaceutical industry.
  • Background that includes knowledge/experience in GMP, GLP, and GCP.
  • Experience with FDA audits is highly preferred.
  • Strong knowledge of GMP and ICH requirements.
  • Must be a self-starter and capable of working with minimal oversight.
  • Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately.
  • Excellent oral and written communication skills.

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.
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