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Overnight Biotech Quality Control Jobs (NOW HIRING)

Legend Biotech USA, Inc.

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Role OverviewThe Supervisor, QC Micro is an exempt level position with responsibilities for ...

Legend Biotech USA, Inc.

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Legend Biotech is seeking QC Analyst II as part of the Quality team based in Raritan, NJ.Role ...

Legend Biotech USA, Inc.

$24.50 - $33/hr

Legend Biotech entered into a global collaboration agreement with Janssen, one of the ... Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ.Role ...

BioPhase Solutions

QC Inspector

San Diego, CA · On-site

$18 - $19.80/hr

Quality Control Inspector Are you passionate about ensuring the highest quality standards in the biotech industry? We are seeking a skilled and detail-oriented Quality Control Technician to join our ...

Legend Biotech USA, Inc.

Legend Biotech is seeking a Sr. Manager, QC Microbiology as part of the Quality team based in Raritan, NJ.Role OverviewThe Sr. Manager, QC Microbiology, is an exempt level position with ...

Poly-America

Overnight Quality Control

Grand Prairie, TX

$18 - $23/hr

P. is currently seeking a Quality Control Technician. Poly-America produces several lines of polyethylene products including high quality trash bags, construction and agricultural films. Quality ...

Poly-America

Overnight Quality Control

Grand Prairie, TX · On-site

$18 - $23/hr

P. is currently seeking a Quality Control Technician. Poly-America produces several lines of polyethylene products including high quality trash bags, construction and agricultural films.

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How much do overnight biotech quality control jobs pay per hour?

As of May 30, 2026, the average hourly pay for overnight biotech quality control in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Overnight Biotech Quality Control professional, and why are they important?

To thrive as an Overnight Biotech Quality Control professional, you need a strong background in biology or chemistry, attention to detail, and familiarity with quality assurance practices, often supported by a relevant bachelor's degree. Proficiency in laboratory equipment, data analysis software, and compliance with regulatory standards like GMP or ISO is typically required. Strong problem-solving skills, reliability, and effective communication are important soft skills for this role. These skills are crucial to ensure consistent product quality, regulatory compliance, and effective issue resolution during overnight operations.

What are some common challenges faced by overnight Biotech Quality Control professionals, and how can they be managed?

Overnight Biotech Quality Control professionals often encounter challenges such as working with limited onsite support, maintaining focus during late hours, and responding quickly to unexpected results or equipment issues. Effective communication with day-shift teams and thorough documentation are essential to ensure continuity and avoid errors. Establishing a consistent routine, prioritizing tasks, and utilizing available digital resources can help manage the unique demands of this role and ensure the accuracy and reliability of quality control results.

What are Overnight Biotech Quality Control jobs?

Overnight Biotech Quality Control jobs involve performing laboratory tests and inspections on biotechnology products during nighttime or overnight shifts. These professionals ensure that products such as pharmaceuticals, biologics, or laboratory samples meet quality and safety standards before they reach the market. Responsibilities often include running assays, documenting results, maintaining equipment, and following strict protocols and Good Manufacturing Practices (GMP). Working overnight helps maintain round-the-clock quality assurance in fast-paced biotech environments. Candidates typically need a background in biology, chemistry, or related fields and attention to detail.

What is the difference between Overnight Biotech Quality Control vs Microbiologist?

AspectOvernight Biotech Quality ControlMicrobiologist
CredentialsBachelor's in biology, microbiology, or related field; GMP trainingBachelor's or higher in microbiology, biology, or related field; lab certifications
Work EnvironmentLaboratory setting, often overnight shifts, regulated biotech facilitiesLaboratory, research, or clinical settings; may include overnight or day shifts
Industry UsageBiotech, pharmaceutical manufacturing, quality assuranceHealthcare, research institutions, biotech, pharmaceuticals

Overnight Biotech Quality Control specialists focus on testing and ensuring product quality in biotech manufacturing, often working overnight shifts. Microbiologists conduct research, analyze microorganisms, and may work in various settings, including clinical labs. While both roles require microbiology knowledge and lab skills, Quality Control roles emphasize compliance and product safety in biotech environments, whereas Microbiologists may have broader research responsibilities.

More about Overnight Biotech Quality Control jobs
What cities are hiring for Overnight Biotech Quality Control jobs? Cities with the most Overnight Biotech Quality Control job openings:
What are the most commonly searched types of Biotech Quality Control jobs? The most popular types of Biotech Quality Control jobs are:
What states have the most Overnight Biotech Quality Control jobs? States with the most job openings for Overnight Biotech Quality Control jobs include:
What job categories do people searching Overnight Biotech Quality Control jobs look for? The top searched job categories for Overnight Biotech Quality Control jobs are:
Overnight Biotech Quality Control jobs near you
Infographic showing various Overnight Biotech Quality Control job openings in the United States as of May 2026, with employment types broken down into 65% Full Time, 31% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 3% Hybrid, and 1% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.
Quality Control Support Technician

Quality Control Support Technician

Krystal Biotech

Pittsburgh, PA • On-site

$21 - $23/hr

Full-time

Posted 15 days ago

Job description

Quality Control Support Technician
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:
The QC Support Technician provides operational, administrative, and laboratory support within the Quality Control department in a GMP-regulated environment. This role is responsible for supporting routine laboratory operations, sample management activities, inventory control, documentation organization, and general laboratory upkeep to improve overall laboratory efficiency.
The ideal candidate is highly organized, detail-oriented, able to work independently, and capable of following established procedures while supporting a fast-paced laboratory environment.
Responsibilities will include, but are not limited to, the following:
Sample & Material Support
  • Perform sample receipt and sample request fulfillment activities
  • Support aliquoting activities including batch samples, reference standards, and CQP samples
  • Coordinate sample shipments, including stability and manufacturing-related shipments
  • Assist with reagent preparation activities
Laboratory Operations Support
  • Maintain laboratory inventory and consumable stocking
  • Support equipment cleaning and general laboratory organization
  • Perform waste removal and laboratory housekeeping activities
  • Support autoclave and dishware activities, as applicable
  • Perform routine safety checks including safety shower and eyewash inspections
  • Coordinate equipment send-outs and service support activities
Documentation & Administrative Support
  • Scan, organize, and file laboratory documentation
  • Maintain spreadsheets, trackers, and laboratory support logs
  • Assist with data collection and trending activities for laboratory metrics and reports
  • Support meeting scheduling and note-taking activities
  • Assist with ad hoc laboratory studies and operational initiatives
Compliance & Quality Support
  • Follow all GMP, safety, and laboratory procedures
  • Maintain accurate and complete documentation practices
  • Support inspection readiness through organization and maintenance of laboratory records and workspaces
  • Adhere to standard operating procedures and departmental expectations
Requirements and Preferred Qualifications: 
  • High school diploma or equivalent required; Associate degree in life science or related field preferred
  • Valid driver’s license required for occasional travel between company sites
  • Experience working in a regulated environment (GMP, GLP, ISO, or similar)
  • Familiarity with laboratory inventory systems and sample tracking
  • Experience supporting laboratory operations or scientific teams
  • Experience with documentation scanning, filing, and archival processes

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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