1,069 Pharmaceutical Qa jobs in the Philippines

Position Title
: Quality Assurance Auditor

Location
: Alabang, Muntinlupa City

Setup
: Onsite

Schedule
: Rotating Shift

Qualifications:

• Bachelor's degree in any 4-year course
• Proven experience in Quality Assurance, preferably within the US Insurance or Health Care industry
• 2 to 3 years of hands-on QA experience is preferred
• Advanced proficiency in Microsoft Excel, including reporting, dashboard creation, and data management
• Strong verbal and written communication skills

Job Description:

Under the supervision of the Operations Supervisor, the Quality Assurance Auditor is responsible for ensuring the accuracy and integrity of client-facing documents by thoroughly reviewing Excel-based proposals and their source materials for errors or discrepancies that could lead to financial exposure. This role requires a strong understanding of employee benefits across medical and ancillary lines, as well as the ability to interpret Carrier Renewals, Quotes, Summary of Benefits and Coverage (SBCs), and benefit summaries.

Responsibilities

• Review client-facing and internal documents (renewals, quotes, presentations) for accuracy and consistency.
• Verify and correct benefits, census data, and rates to prevent financial or reputational risks.
• Ensure alignment of documents with carrier information and company standards.
• Interpret and validate benefit summaries across medical, dental, vision, life, disability, and ancillary products.
• Collaborate with internal teams to resolve benefit inconsistencies.
• Prepare and manage broker compensation disclosure forms in D365, ensuring regulatory compliance.
• Convert Excel proposals to PDF, deliver to clients via email, and upload to the Simple Booklet system.
• Adhere to company policies on quality, security, safety, environment, and data privacy.
• Address audit findings, corrective actions, and report security incidents promptly.
• Perform other assigned duties.

QUALITY ASSURANCE SPECIALIST - Pacific Destinations

Job Type: Full Time-Individual Contributor 

Location: Goway Manila 

Reporting to: QA Manager

Job purpose:

INA Prime Solutions is our BPO line of business in Manila, PH at Goway Travel Ltd. Our mission is to empower businesses through seamless outsourcing solutions, leveraging skilled workforce to drive operational excellence and client success.

As a Quality Assurance for Pacific Destinations team,

What will be your key responsibilities?

1. Review, evaluate, and score loaded contracts, confirmations and documentation etc. against established quality assurance standards.
2. Participate, as needed, in calibration sessions, employee communication sessions, and/or creation of communication tools
3. Supports and communicates business goals, quality standards, processes and procedures and policies
4. Ensure agents adhere to quality assurance standards and standard operating procedures.
5. Analyze data and metrics to assess the quality of operations and identify trends or patterns.
6. Collaborate with cross-functional teams to implement quality improvement initiatives.
7. Conduct coaching sessions as needed
8. Provides performance expectations, action plans and development plans to improve quality
9. Monitor and evaluate the effectiveness of quality improvement initiatives.
10. Provides accurate and timely reports on a daily, monthly, month-to-date and year-to-date rolling basis on call quality, productivity, availability and other key metrics as determined
11. Provide training and support to team members to ensure compliance with quality standards.
12. Develop and implement strategies to improve operational efficiency and quality.

What are we looking for?

• Demonstrated experience in contract loading or quality assurance roles.
• Proven track record of strong analytical skills and data interpretation.
• Hands-on experience in quality assurance processes and procedures is a plus.
• Excellent interpersonal skills with the ability to communicate feedback effectively.
• Strong organizational skills and knowledge of goal-setting practices.
• Proficiency in data visualization techniques and understanding of support metrics.
• Understanding of basic business metrics and the impact of support on overall
• Ability to solve problems and develop effective strategies to enhance support
• Willingness to train onsite

Preferred Qualifications:

• Experience in BPO
• Proficient in Excel and Google Sheets

What can you expect from Goway?Imagine working for a company where your career feels like an adventure. At Goway, you'll join a global community that supports one another:

• We offer a competitive salary accompanied by performance incentives, and we place real importance on time away from work, such as paid personal days for when life calls for them and your birthday off each year.
• Your future matters to us, so we match your RRSP contributions and provide comprehensive medical, dental, and vision coverage.
• Our commitment to professional growth means you'll have access to continuous learning and industry-leading training that keeps you at the forefront of travel innovation.
• Travel is in our DNA, so you'll enjoy exclusive perks and discounts on worldwide getaways.
• Since we operate across Toronto, Vancouver, Los Angeles, Manila, Sydney, and beyond, you'll collaborate across cultures and shape a career path that reflects your ambitions.
• Goway is an equal-opportunity employer. We celebrate differences and are committed to fostering an inclusive workplace for everyone. We appreciate every applicant's interest. Please be advised that only those selected for an interview will be contacted.

How to Apply:

If this role feels like your next step, click "Apply Now" to create your profile, upload your CV, and share a few details about yourself. Our talent team reviews every application, and if your experience aligns with our needs, we will reach out to set up the next step.

Recruitment scams & fraud warning:

Please be aware of any suspicious emails or WhatsApp activity from individuals pretending to be recruiters or senior personnel at Goway Travel. We will never ask you to install an app during the recruitment process. If you receive a message of this nature, please ignore it and report it to Goway.

About Goway

Founded in Toronto in 1970 by Australian economist Bruce Hodge, Goway has evolved from a one-person dream into a family-owned global leader in tailor-made travel. With our headquarters in Toronto and hubs in Vancouver, Los Angeles, Sydney, and Manila, our team of over 700 talented employees designs travel experiences in more than 115 countries across all seven continents. We're united by a passion for travel and are committed to doing the right thing: supporting diversity, equity, inclusion, and sustainable tourism that enriches local communities. Whether working remotely or side by side in one of our offices, we operate as one forward-thinking team, transforming wanderlust into life-changing adventures for our fellow Globetrotters. Discover more

• Performs microbiological and physical-chemical tests of raw materials, finished products and environmental tests of all food safety related equipment and facilities
• Ensures that Good Laboratory Practices and the Quality Assurance Systems are strictly implemented and in place
• Conducts GMP of production and personnel
• Implements HACCP Plan and pre-requisite programs
• Maintaining detailed records and documentation to ensure compliance with industry regulations and internal standards

Job description:

Job Summary:

We are seeking a dedicated and detail-oriented Quality Assurance Specialist to join our team. The ideal candidate must have a solid background in the pharmaceutical industry and will be responsible for ensuring full compliance with Good Manufacturing Practices (GMP), regulatory standards, and company quality protocols. This role plays a key part in maintaining the integrity and quality of our products and processes.

Qualifications:

• Graduate of BS Pharmacy, Applied Science, or Chemical Engineering
  
  – Must hold a bachelor's degree in Pharmacy, Applied Science, Chemical Engineering, or a closely related field, providing a solid foundation in scientific principles and technical knowledge relevant to pharmaceutical operations.
• Preferably with prior experience in QA/QC or regulatory functions within the pharmaceutical industry
  
  – Candidates who have hands-on experience in Quality Assurance, Quality Control, or regulatory compliance in a pharmaceutical manufacturing environment are highly preferred, as this ensures familiarity with industry standards and requirements.
• Dossier preparation and regulatory submission experience is an advantage
  
  – Exposure to preparing technical dossiers, handling documentation, and coordinating regulatory submissions to local or international agencies will be considered an added asset.
• Strong analytical, problem-solving, and critical thinking skills
  
  – Must be capable of identifying issues, analyzing data, evaluating possible solutions, and making sound decisions to support the company's compliance and quality objectives.
• Excellent English communication skills, both written and verbal
  
  – Should demonstrate strong proficiency in written and spoken English, with the ability to prepare accurate reports, draft professional correspondence, and communicate effectively with internal teams and external regulatory bodies.
• Computer literate, with proficiency in Microsoft Office tools
  
  – Proficiency in MS Word, Excel, PowerPoint, and other Microsoft Office applications is required for documentation, reporting, and presentation of data in a clear and professional manner.
• Highly organized, detail-oriented, and capable of managing multiple tasks
  
  – Must possess strong organizational skills with the ability to prioritize workload, handle multiple projects simultaneously, and maintain accuracy and attention to detail in all tasks.
• Self-motivated, goal-oriented, and able to work both independently and collaboratively
  
  – Should be proactive, driven to achieve results, and capable of working efficiently on individual assignments while also being an effective team player in collaborative projects.

Key Responsibilities:

• Ensure compliance with GMP guidelines and internal quality standards across all operations
• Oversee regulatory submissions including FDA applications and product registrations
• Prepare, review, and maintain documentation related to QA activities, audits, and compliance reports
• Assist in identifying areas for improvement and participate in the implementation of corrective and preventive actions (CAPA)
• Draft and update Standard Operating Procedures (SOPs), training materials, and quality manuals
• Collaborate with cross-functional departments to resolve product and process-related quality issues
• Participate in internal audits, inspections, and continuous quality improvement initiatives

Job Title: Quality Assurance (QA) Specialist

Location: Remote-Philippines

Employment Type: Full-Time, Independent Contractor

Department: Operations

Reporting to: Ecommerce Project Manager

About the Company

310 Nutrition is a trusted leader in health and wellness, delivering high-quality, clean-ingredient products designed to help individuals reach their healthiest potential. As a digital-first company, we prioritize exceptional user experiences across our e-commerce platform and digital assets, making quality assurance a cornerstone of our success.

Role Overview

The Quality Assurance (QA) Specialist will ensure the functionality, usability, and responsiveness of our digital products across different devices, screen sizes, and browsers. Collaborating closely with developers, designers, and project managers, you will identify and resolve issues, ensuring a seamless and high-quality user experience.

Key Responsibilities

Testing & Quality Assurance:

• Conduct functional, regression, and usability testing on websites, applications, and digital platforms.
• Perform cross-browser and cross-device testing (desktop, mobile, tablet) to ensure optimal responsiveness.
• Identify, document, and track bugs, inconsistencies, and usability issues.
• Ensure products meet design specifications and work seamlessly across different environments.
• Test performance, page speed, and accessibility across devices.

Collaboration & Process Improvement:

• Work closely with developers and designers to address bugs and inconsistencies.
• Provide clear, structured feedback to improve product quality.
• Align quality assurance processes with user experience (UX) and conversion rate optimization (CRO) best practices.
• Develop and maintain QA documentation, test cases, and testing reports.
• Collaborate with project managers to ensure deadlines are met while maintaining quality.

Efficiency & Optimization:

● Suggest improvements for testing tools, techniques, and workflows to enhance the QA process.

Qualifications

• Proven experience as a QA Specialist, Tester, or similar role.
• Strong understanding of UI/UX principles and ability to spot visual inconsistencies.
• Experience in cross-browser and cross-device testing (e.g., Chrome, Firefox, Safari, Edge, mobile devices).
• Familiarity with responsive design testing tools like BrowserStack or LambdaTest.
• Attention to detail and the ability to provide clear, concise bug reports.
• Strong communication skills for collaboration with designers, developers, and project managers.
• Experience with test case creation and issue tracking tools like ClickUp.
• Basic knowledge of HTML, CSS, and JavaScript (preferred but not required).
• Understanding of performance testing, accessibility standards, and SEO best practices (preferred).

Preferred Qualifications

• Experience with ClickUp for task and workflow management.
• Familiarity with Shopify and WordPress for e-commerce and website testing.
• Knowledge of QA automation tools.
• Understanding of Agile/Scrum methodologies.

Proficiency in the following applications is a PLUS:

Pingdom / UptimeRobot

• These primarily monitor page availability and load performance.
• They're good for uptime, not for true transactional testing.

Checkly

• Checkly allows you to build custom end‑to‑end scripts (using Puppeteer/Playwright under the hood).
• You can simulate parts of the checkout, but Shopify checkout itself is tricky because: ○ Shopify checkout often requires real payment tokens.

○ Shopify's hosted checkout limits automation for security/PCI compliance.

Datadog Synthetic Monitoring

• Simulates real user journeys (a.k.a. "synthetic tests") on your site.
• Example: Automatically "pretend" to be a user by loading homepage → cart → checkout flow and measuring response times or errors.
• Detects issues like broken steps in the funnel, slow pages, or unexpected responses. Use it when: You want to proactively catch functional or performance issues before customers do.

Sentry

• Captures JavaScript errors or exceptions happening in live sessions.
• Shows stack traces, browsers affected, and frequency so devs can debug quickly.

Use it when: You need to know if users are encountering console errors, broken scripts, or other code problems in production.

Hexowatch (or Visualping)

• Monitor visual changes on your site.
• Example: If your homepage layout suddenly shifts, a banner disappears, or a CTA button breaks, these tools alert you.
• They compare screenshots over time and flag unexpected changes.

Use it when: You need to ensure critical pages (homepage, checkout, promo pages) stay visually intact after updates or deploys.

Visualping (alternative to Hexowatch)

• Also, for visual change detection on specific URLs.
• Simpler and often cheaper than Hexowatch.
• Sends alerts (email, Slack) when something on a page changes compared to its last snapshot.

Use it when: You want lightweight visual monitoring for key pages or elements.

What We Offer

• Competitive compensation tailored to the QA Specialist role.
• Innovation-driven culture with opportunities to enhance workflows using the latest tools.
• Flexible, remote work setup with a global, supportive team.
• Opportunities for professional growth in a fast-paced digital environment.

Job Type: Full-time

Pay: From Php60,000.00 per month

Benefits:

• Flexible schedule
• Work from home

Application Question(s):

• Do you have a background in e-commerce or digital marketing (wellness, health, or skincare industry)?

• Would you be comfortable with the use of Teramind, a remote work monitoring tool?

• Can you work on a full-time basis as an independent contractor? 40 hours a week.

• As an independent contractor, do you have your own laptop and stable internet connection suitable for full-time remote work?
• Have you used any of the following tools? If so, how did you apply them in QA?

ClickUp (task management)

Sentry (JavaScript error tracking)

Hexowatch / Visualping (visual monitoring)

Pingdom / UptimeRobot

Checkly / Datadog Synthetic Monitoring

Work Location: Remote

QA Specialist - FIELD

Job Description:

Facilitates timely and proper conduct of independent appraisal of the effectiveness of the policies, procedures and standards of the company's resources and operations.

• Provide relevant assistance on planning and scheduling on a timely and appropriate design of all QAFA activities, and provide technical assistance on the other member of the team
• Responsible and provide clear direction for the strict implementation of food safety procedures and standards in all stores and restaurant operations
• Provide clear and timely preparation of complete and accurate analysis, appraisals, recommendations on audit findings and results that can influence or convince both internal and external unit and have a positive strong impact within the department or on other operations
• Ensure fair and objective detection of non- compliances with regards on food safety standards and policies
• Provide and strict observance on proper implementation of an approved clear procedure to improve operational system and process
• Provides clear recommendations and assistance on removal of inventory items that are obsolete or damaged or expired to ensure that no stock is kept in circulation that is out of date or below par the company's quality standard.
• Facilitate on proper documentation and validation of internal and external complaint
• Facilitate food safety refresher course training to all sales personnel

Job Qualifications:

• Graduate of BS Food technology
• Preferably with experience in the meat industry
• Familiar with restaurant service
• Trainings: GMP, HACCP, SSOP, ServSafe

Deployment Location: Olongapo - Subic area

Job Types: Full-time, Permanent, Fresh graduate

Pay: Php18, Php26,000.00 per month

Benefits:

• Company events
• Flexible schedule
• Flextime
• Opportunities for promotion
• Paid training
• Pay raise
• Promotion to permanent employee

Ability to commute/relocate:

• Olongapo: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Required)

Work Location: In person

Job Purpose and Impact

The QA Specialist - Materials Receiving (Licensed Chemical Technician) will complete moderately complex analytical and laboratory testing in support of the food safety quality and operational teams. In this role, you will perform routine analysis of product testing and will check and monitor instrumentation performance, conduct tests and document results into databases and communicate test results.

Key Accountabilities

• Conduct routine quantitative and qualitative inspections and laboratory tests on raw materials, in process and final products independently and support more complex trials and experiments under intermediate supervision.
• Ensure compliance programs for all individual testing, which includes monitoring adherence to regulations and other procedural food safety compliance.
• Interpret and document results of tests into active databases and communicate results to internal customers as required.
• Run calibration checks, preventive maintenance tasks and simple repair to analytical instrumentation and maintain customer specifications books.
• Help develop food and feed safety, quality and regulatory culture and collaborate cross functionally to build, maintain and improve an effective food safety, quality and regulatory culture.
• Handle moderately complex clerical, administrative, technical or customer support issues under general supervision, while escalating more complex issues to appropriate staff.
• Other duties as assigned

Qualifications
Minimum Qualifications

• Licensed Chemical Technician
• Minimum requirement of 2 years of relevant work experience.

Preferred Qualifications

• Ability to read and interpret documents (safety rules, operating and maintenance instructions, and procedure manuals).
• Licensed Chemist
• Strong computer program professional knowledge: Microsoft Word, Excel, Access and Outlook.
• Write routine reports and correspondence.

• Bachelor's degree in Food Technology, Biology, Chemistry, Chemical Engineering, or a related field required.
• PRC Licensed Professional Food Technologist, Chemical Technician or Chemist.
• At least 1 year of experience in quality assurance or a related field within the food and beverage industry.
• Experience with quality management systems, audits, and regulatory compliance.
• Strong understanding of GMP, Hazard Control Plan, QFSMS and food safety regulations.

Job description:

Job Summary:

We are seeking a dedicated and detail-oriented Quality Assurance Specialist to join our team. The ideal candidate must have a solid background in the pharmaceutical industry and will be responsible for ensuring full compliance with Good Manufacturing Practices (GMP), regulatory standards, and company quality protocols. This role plays a key part in maintaining the integrity and quality of our products and processes.

Qualifications:

• Graduate of BS Pharmacy, Applied Science, or Chemical Engineering

– Must hold a bachelor's degree in Pharmacy, Applied Science, Chemical Engineering, or a closely related field, providing a solid foundation in scientific principles and technical knowledge relevant to pharmaceutical operations.

• Preferably with prior experience in QA/QC or regulatory functions within the pharmaceutical industry

– Candidates who have hands-on experience in Quality Assurance, Quality Control, or regulatory compliance in a pharmaceutical manufacturing environment are highly preferred, as this ensures familiarity with industry standards and requirements.

• Dossier preparation and regulatory submission experience is an advantage

– Exposure to preparing technical dossiers, handling documentation, and coordinating regulatory submissions to local or international agencies will be considered an added asset.

• Strong analytical, problem-solving, and critical thinking skills

– Must be capable of identifying issues, analyzing data, evaluating possible solutions, and making sound decisions to support the company's compliance and quality objectives.

• Excellent English communication skills, both written and verbal

– Should demonstrate strong proficiency in written and spoken English, with the ability to prepare accurate reports, draft professional correspondence, and communicate effectively with internal teams and external regulatory bodies.

• Computer literate, with proficiency in Microsoft Office tools

– Proficiency in MS Word, Excel, PowerPoint, and other Microsoft Office applications is required for documentation, reporting, and presentation of data in a clear and professional manner.

• Highly organized, detail-oriented, and capable of managing multiple tasks

– Must possess strong organizational skills with the ability to prioritize workload, handle multiple projects simultaneously, and maintain accuracy and attention to detail in all tasks.

• Self-motivated, goal-oriented, and able to work both independently and collaboratively

– Should be proactive, driven to achieve results, and capable of working efficiently on individual assignments while also being an effective team player in collaborative projects.

Key Responsibilities:

• Ensure compliance with GMP guidelines and internal quality standards across all operations
• Oversee regulatory submissions including FDA applications and product registrations
• Prepare, review, and maintain documentation related to QA activities, audits, and compliance reports
• Assist in identifying areas for improvement and participate in the implementation of corrective and preventive actions (CAPA)
• Draft and update Standard Operating Procedures (SOPs), training materials, and quality manuals
• Collaborate with cross-functional departments to resolve product and process-related quality issues
• Participate in internal audits, inspections, and continuous quality improvement initiatives

Job Types: Full-time, Fresh graduate

Work Location: In person