1

Qa Technical Lead Jobs (NOW HIRING)

Role Summary The Associate Director, QA Operations serves as the QA technical lead for external manufacturing and testing project teams, ensuring the effective development, implementation, and ...

Showing results 41-60

Qa Technical Lead information

See salary details

$30K

$156.3K

$206K

How much do qa technical lead jobs pay per year?

As of Sep 2, 2026, the average yearly pay for qa technical lead in the United States is $156,348.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,000.00 and $205,000.00 per year, depending on experience, location, and employer.

What is the difference between Qa Technical Lead vs Qa Analyst?

AspectQa Technical LeadQa Analyst
Required CredentialsTypically requires a QA certification, experience in automation and scripting, and technical expertiseOften requires a QA certification or degree, focus on manual testing skills, and basic automation knowledge
Work EnvironmentLeads testing teams, collaborates with developers, and oversees automation frameworksPerforms testing, documents defects, and executes test cases
Employer & Industry UsageCommon in software development companies, tech firms, and enterprises with complex testing needsUsed across various industries including software, finance, and healthcare for quality assurance

The Qa Technical Lead focuses on leading testing efforts, automation, and technical oversight, while the Qa Analyst primarily executes manual tests and documents results. Both roles are essential in ensuring software quality but differ in scope and technical responsibilities.

Is a QA Technical Lead a stressful job?

A QA Technical Lead role can be stressful due to deadlines, high-quality standards, and coordinating testing efforts across teams. Managing complex projects and ensuring software reliability often requires strong organizational and communication skills, which can contribute to work pressure.

What is a QA Technical Lead?

A QA Technical Lead is a senior quality assurance professional responsible for overseeing testing processes, developing testing strategies, and guiding QA teams to ensure software quality. They often have expertise in automation tools, scripting, and testing frameworks, and collaborate closely with development teams to identify and resolve issues efficiently.
More about Qa Technical Lead jobs
Infographic showing various Qa Technical Lead job openings in the United States as of August 2026, with employment types broken down into 60% Full Time, and 40% Contract. Highlights an 100% In-person job distribution, with an average salary of $156,348 per year, or $75.2 per hour.

Quality Assurance Technical Reviewer

Mentor Technical Group

Vega Baja, PR • On-site

$70 - $90/hr

Other

Re-posted 21 days ago


Job description

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG ensures compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Responsibilities

Review and audit validation, qualification, and verification activities across manufacturing, packaging, utilities, facilities, laboratories, and systems.

Participate in defining validation/qualification strategies for product transfers and site product changes, including regulatory impact assessments.

Review and approve Operational Qualification (OQ), Performance/Process Qualification (PQ), and Verification activities, along with associated SOPs.

Review and approve analytical test method validation/verification reports, specifications, test methods, laboratory instrument qualifications, periodic reviews, risk assessments, commissioning documentation, installation certifications, and master batch records for manufacturing and packaging.

Coordinate Change Requests (CRs) for qualified production records, equipment, systems, and facilities, including review, tracking, safekeeping, and closure of CRs.

Assess the regulatory impact of proposed changes and ensure completeness of documentation prior to approval.

Support PCF sponsors in preparing change requests by providing regulatory documentation.

Create and revise export profiles for assigned products.

Support activities related to new R&D products, including change controls, development, and validation documentation.

Contribute to the APR process.

Review documentation and change controls related to shipping labels and artwork.

Qualifications / Requirements / Knowledge / Skills

Bachelor’s or Master’s degree in Chemical Engineering, Pharmaceutical Technology, or a related scientific field.

Proven experience in validation, qualification, and verification within a pharmaceutical manufacturing environment.

Strong knowledge of current Good Manufacturing Practices (cGMP) and other regulatory requirements.

Experience with Change Control processes, regulatory impact assessments, and cross-functional coordination.

Excellent skills in reviewing, auditing, and writing technical documentation.

Ability to manage multiple projects and prioritize tasks effectively.

Strong analytical, problem-solving, and communication skills.

Proficient in MS Office applications (Word, Excel, PowerPoint, etc.).

Bilingual: fluent in English and Spanish preferred.

Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

#J-18808-Ljbffr