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Intermediate Qa Analyst Jobs in Humacao, PR (NOW HIRING)

Amgen

Sr Associate QA

Juncos, PR · On-site

Analyze data and documentation to detect trends or potential quality issues, escalating ... Intermediate word processing, database, presentation and spreadsheet application skills * Skill in ...

ProQualityNetwork

QA Specialist-35615

Juncos, PR

Strong analytical skills with the ability to assess compliance risks and recommend appropriate ... Quality Assurance program under minimal supervision. FUNCTIONS - Review and approve product MPs ...

New

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance ... analysis, documenting investigation activities, and preparing clear, evidence-based inputs for ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance ... analysis, documenting investigation activities, and preparing clear, evidence-based inputs for ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance ... analysis, documenting investigation activities, and preparing clear, evidence-based inputs for ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance ... analysis, documenting investigation activities, and preparing clear, evidence-based inputs for ...

Danaher

Quality Assurance Specialist II

Fajardo, PR · On-site

This position reports to the Sr. Manager QA Engineering and is part of the Quality Assurance ... analysis, documenting investigation activities, and preparing clear, evidence-based inputs for ...

Mirus Consulting Group

Specialist QA - 35615

Juncos, PR · On-site

Position Summary The Specialist QA is responsible for ensuring compliance with quality standards ... Strong analytical, problem-solving, and organizational skills. * Excellent written and verbal ...

New

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Intermediate Qa Analyst information

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How much do intermediate qa analyst jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for intermediate qa analyst in Humacao, PR is $40.54, according to ZipRecruiter salary data. Most workers in this role earn between $28.94 and $50.14 per hour, depending on experience, location, and employer.

What is the difference between Intermediate Qa Analyst vs QA Tester?

AspectIntermediate QA AnalystQA Tester
CredentialsTypically requires a bachelor's degree in IT, Computer Science, or related field; certifications like ISTQB are commonOften requires a high school diploma or associate degree; certifications like ISTQB are also common but less emphasized
Work EnvironmentInvolves analyzing requirements, designing test plans, and coordinating testing efforts within development teamsPrimarily executes test cases, reports bugs, and documents test results, often under supervision
Industry UsageUsed across software development, IT, and tech companies for quality assurance rolesCommonly found in software companies, testing service providers, and tech industries

The Intermediate QA Analyst typically has more responsibilities in test planning, analysis, and coordination, requiring a higher level of technical knowledge and experience. QA Testers focus more on executing tests and identifying bugs. Both roles are essential in quality assurance but differ in scope and complexity.

What are the key skills and qualifications needed to thrive as an intermediate QA analyst?

To thrive as an Intermediate QA Analyst, you need a solid understanding of software testing methodologies, test case design, and defect tracking, typically supported by a degree in computer science or related experience. Familiarity with automated testing tools (such as Selenium or JUnit), bug tracking systems like Jira, and knowledge of SQL are commonly required. Strong attention to detail, analytical thinking, and effective communication help QA Analysts identify issues and collaborate with development teams. These skills and attributes are crucial to ensure software quality, reduce defects, and deliver reliable products to end users.

What is an intermediate QA analyst?

Intermediate QA Analysts are quality assurance professionals with a moderate level of experience, typically ranging from 2 to 5 years. They are responsible for designing, implementing, and executing test plans and cases to ensure software meets quality standards. Intermediate QA Analysts work closely with developers, product managers, and other stakeholders to identify bugs, verify fixes, and contribute to process improvements. Their role often involves both manual and automated testing, and they are expected to have a solid understanding of QA methodologies and tools.

What are some typical challenges faced by an intermediate QA analyst when working on cross-functional teams?

As an Intermediate QA Analyst, one common challenge is ensuring clear communication and alignment between developers, product managers, and other stakeholders. You may need to advocate for quality standards while managing tight deadlines and shifting requirements. Balancing thorough test coverage with project timelines and adapting to evolving technologies are also frequent hurdles. Collaborating effectively and proactively addressing issues helps maintain both software quality and team efficiency.
Intermediate Qa Analyst jobs near you

Specialist QA

BioPharma Consulting JAD Group

Juncos, PR • On-site

Full-time

Re-posted 19 days ago

Job description

Under minimal supervision, the Specialist QA supports the site Quality Assurance program by ensuring compliance with cGMP requirements, regulatory standards, and internal quality systems. The role provides oversight across manufacturing, environmental monitoring, critical utilities, validation, and quality systems, while driving continuous improvement and maintaining a strong contamination control posture.

FUNCTIONS

  • Review and approve product MPs, process validation protocols, and validation reports.
  • Review and approve Work Orders, EMS/BMS alarms, nonconformance investigations, CAPA records, and change controls.
  • Approve Environmental Characterization reports and planned incidents.
  • Provide lot disposition and authorize lots for shipment.
  • Lead investigations, site audits, and own site quality program procedures.
  • Serve as QA designee on local CCRB and represent QA on NPI teams.
  • Participate in incident triage teams and support automation, facilities, and environmental programs.
  • Review and assess risk assessments across GMP operations.
  • Ensure facilities, equipment, materials, processes, and products comply with cGMP and applicable regulations.
  • Support internal and external audits and inspections.
  • Alert senior management of quality, compliance, supply, and safety risks.
  • Support GMP building Environmental Monitoring (EM) processes.
  • Generate EM and Critical Utilities (CU) trend reports; analyze data to identify improvement opportunities.
  • Lead or participate in risk assessments for sampling sites in GMP areas.
  • Provide quality assessments for change controls, deviations, audits, and contamination control initiatives.
  • Participate in Environmental Control Network, Aseptic Council, and Contamination Control Network.
  • Present EM/CU data and recommendations during Quality System forums and Management Review meetings.
  • Ensure adherence to regulatory standards including Annex 1, FDA Guidance, ISO‑14644‑1, and USP.
  • Support continuous improvement initiatives related to contamination control and environmental programs.

COMPETENCIES & SKILLS

  • Strong knowledge of QA, QAL, validation, process development, and GMP manufacturing.
  • Advanced data trending, evaluation, and compliance issue assessment.
  • Experience in EM, Microbial Identification, CU monitoring, sampling techniques, and microbiological testing methods.
  • Understanding of aseptic behavior, facility cleaning/disinfection, and contamination control strategies.
  • Ability to interpret and apply regulatory requirements for cleanrooms and controlled environments.
  • Proficiency in Microsoft Office (Word, PowerPoint, Excel), Smartsheets, and data visualization tools.
  • Hands-on experience with electronic systems such as Veeva, Spotfire, LIMS, Maximo.
  • Ability to use statistical tools and AI/data analytics platforms to interpret EM/CU data.
  • Strong project management and organizational skills.
  • Ability to lead cross-functional teams, influence stakeholders, and negotiate effectively.
  • Strong written and oral communication skills; facilitation and presentation capabilities.
  • Fully bilingual in English and Spanish.
  • Demonstrated ability to interact with regulatory agencies.
  • Ability to work independently and collaborate across multiple levels of the organization.
  • Demonstrates strong leadership practices and quality mindset.

Requirements

EDUCATION REQUIREMENTS

  • Doctorate OR
  • Master’s + 2 years directly related experience OR
  • Bachelor’s + 4 years directly related experience OR
  • Associate’s + 8 years directly related experience OR
  • High School/GED + 10 years directly related experience

Preferred:

  • Bachelor’s or higher in Microbiology, Biology, Life Sciences, Engineering, Chemistry, Physics, or Computer Science.
  • 10+ years in biopharmaceutical industry with 5+ years in Quality.

PREFERRED QUALIFICATIONS

  • Extensive experience in Quality & Compliance, regulatory audits, validation, characterization, and automation validation.
  • Strong background in reviewing/approving deviations, EM/CU trend reports, and contamination control documentation.
  • Ability to identify quality, compliance, supply, and safety risks and escalate appropriately.

Benefits

  • Administrative Shift
  • 1 Year contract