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Biotech Qa Jobs (NOW HIRING)

DivIHN

QA Contractor, GMP Quality Assurance

NC · On-site

... biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement * Strong understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S ...

Krystal Biotech

Quality Assurance Associate

Moon, VA · On-site

About Krystal Bio At Krystal Biotech, we bring together the brightest and most eager minds to ... Provide oversight of daily QA functions which include review and approval of records generated by ...

Legend Biotech US

Director, QA Operations

Raritan, NJ · On-site

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Legend Biotech is seeking a Director, QA Operations as part of the Quality team based in Raritan ...

Legend Biotech USA

Director, QA Operations

Raritan, NJ · On-site

Legend Biotech is seeking a Director, QA Operations as part of the Quality team based in Raritan, NJ. Role Overview The Director of Quality Operations, CAR-T is responsible for Quality oversight and ...

Legend Biotech USA, Inc.

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Legend Biotech is seeking a Director, QA Operations as part of the Quality team based in Raritan ...

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

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

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 ...

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Biotech Qa information

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$10

$46

$73

How much do biotech qa jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for biotech qa in the United States is $46.70, according to ZipRecruiter salary data. Most workers in this role earn between $29.81 and $62.02 per hour, depending on experience, location, and employer.

What is a Biotech QA?

Biotech QA (Quality Assurance) professionals are responsible for ensuring that products developed in the biotechnology industry meet regulatory standards and quality requirements. They oversee processes to ensure compliance with Good Manufacturing Practices (GMP), conduct audits, review documentation, and collaborate with other departments to maintain product integrity. QA professionals play a critical role in preventing errors, ensuring safety, and facilitating the approval of biotech products by regulatory agencies like the FDA. Their work helps protect consumers and supports the successful commercialization of new biotechnological innovations.

What are the key skills and qualifications needed to thrive as a Biotech QA?

To thrive as a Biotech QA, you need a strong background in life sciences, quality assurance processes, and regulatory compliance, often supported by a relevant degree and experience in biotech or pharmaceuticals. Familiarity with quality management systems (QMS), Good Manufacturing Practices (GMP), and tools like LIMS or CAPA systems is typically required, with certifications such as ASQ CQE being advantageous. Strong attention to detail, problem-solving abilities, and effective communication skills are essential soft skills for this role. These competencies ensure that biotech products meet stringent regulatory standards and maintain high quality, safeguarding consumer safety and company reputation.

What are some common challenges faced by Biotech QA professionals when ensuring compliance with industry regulations?

Biotech QA professionals often encounter challenges such as staying up-to-date with evolving regulatory requirements, managing complex documentation, and ensuring consistency across multiple teams and processes. They must balance strict compliance with the need for efficiency in dynamic research and production environments. Collaborating with scientists, engineers, and production staff, QA professionals play a crucial role in identifying potential risks, conducting audits, and implementing corrective actions to maintain product quality and regulatory standards.

What is the difference between Biotech Qa vs Biotech Quality Control Analyst?

AspectBiotech QaBiotech Quality Control Analyst
CredentialsBachelor's in Life Sciences, Quality Certifications (e.g., ASQ)Bachelor's in Life Sciences, Quality Certifications (e.g., ASQ)
Work EnvironmentQuality assurance departments, documentation review, auditsLaboratory testing, sample analysis, data recording
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract labsBiotech and pharmaceutical manufacturing, testing labs

Biotech Qa professionals focus on ensuring overall quality systems, audits, and compliance, while Biotech Quality Control Analysts primarily perform laboratory testing and sample analysis. Both roles require similar credentials and work within biotech environments, but their daily tasks and focus areas differ.

What cities are hiring for Biotech Qa jobs?

Cities with the most Biotech Qa job openings:

What states have the most Biotech Qa jobs?

States with the most job openings for Biotech Qa jobs include:

What are popular job titles related to Biotech Qa jobs?

For Biotech Qa jobs, the most frequently searched job titles are:

Biotech Qa jobs near you
Infographic showing various Biotech Qa job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 89% Full Time, 4% Part Time, 5% Contract, and 1% Nights. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $97,144 per year, or $46.7 per hour.

QA Contractor, GMP Quality Assurance

NC • On-site

DivIHN
See more jobs at DivIHNexternal

Contractor

Re-posted 27 days ago

Job description

For further inquiries regarding the following opportunity, please contact our Talent Specialist, Hema at (630) 847-0275
Title:QA Contractor, GMP Quality Assurance
Location: Onsite at Research Triangle Park, NC
Duration: 9 Months
Travel: Domestic travel (less than 10% of the time) expected.
Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered
Description:
The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or designee, will be responsible for assisting in the management of client Quality Management System (QMS) and will strongly support client's Culture of Quality. This role will assure corporate compliance with applicable GMP national, international, and state regulations. This position will be based at our headquarters facility in RTP, NC.
Job Responsibilities
  • Manage assigned day-to-day QA responsibilities in support of the company's Quality Management Systems (QMS).
  • Provide timely support of Learning Management System, Change Control, Deviation Management Systems, or other QMS based customer requests.
  • Liaison with applicable department record owners to ensure their complete and timely resolution. Review and Approve said record types as assigned.
  • Provide accurate and timely weekly and quarterly QMS metric and Key Performance Indicator updates to QA and CMC senior management.
  • Collaborate successfully with the other departments to ensure that direct and supportive tasks are completed within project timelines.
  • Providing deliverables and resolving issues; Draft SOPs/controlled documents as well as perform quality unit review and approval of Quality Management Systems requests/ records related to Learning Management, Non-Conformance Management, CAPA management, and metric/KPI reporting.
  • Continually evaluate systems and procedures for improvement for efficiency and compliance to applicable regulatory requirements and standards.
  • Participate in project meetings as a Quality Unit representative and support colleagues by acting as a technical resource for quality and compliance related issues.
  • Perform daily customer-facing activities, as assigned by area management.
  • Maintain health of customer-facing activities such as document archival activities and notebook/logbook assignment and management.
  • Identify and collaborate with colleagues to implement continuous improvement initiatives; provide Quality Unit oversight of QMS based activities.
  • Assist in the qualification and oversight of vendors, contract manufacturers, contract laboratories, and service providers.
  • Support regulatory (FDA, EMA) and internal audits/inspections per client procedures and applicable regulatory requirements.
  • Communicate project status to stakeholders and escalate issues in a timely manner.
  • Perform and support other duties as assigned by area management.

About you
  • Bachelor's degree in a scientific field and 4+ years of experience in GMP based Quality Assurance, particularly in support/oversight of a company QMS, or 10+ years of GMP based Quality Assurance experience using a company QMS.
  • 3+ experience working within a pharmaceutical/biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement
  • Strong understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S. standards, and where appropriate, other regulatory authority standards.
  • Ability to author, review, and interpret Standard Operating Procedures (SOPs).
  • Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible, and constructive manner.
  • Strong attention to detail, highly organized and the ability to multitask in a fast-paced, highly interactive environment.
  • Strong service-oriented mindset with excellent verbal and written communication skills, and the ability to effectively collaborate with peers including scientific/technical colleagues.
  • Experience in analytical method validation and QC testing, especially in the fields of mammalian cell culture and Gene Therapy/Biologics based potency testing, is preferred.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

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