1,403 Head Of Quality jobs in the Philippines

JOB DESCRIPTION:

Team Leadership and Organizational Development

• Provide strategic leadership to the quality organizations, aligning departmental goals with overall business objectives.
• Build and develop a high-performing quality leadership team through mentorship, succession planning, and capability development.
• Cultivate a culture of quality and accountability, and continuous improvement across all operational levels and functions.

Enterprise Risk & Compliance Management

• Oversee enterprise wide quality risk identification and mitigation strategies across product, process, and supply chain domains.
• Establish robust governance frameworks for quality risks assessment and ensure alignment with global regulatory and customer compliance requirements.
• Lead cross-functional initiatives to proactively resolve systemic risks and elevate quality resilience.

Quality Performance & Executive Reporting

• Define and drive strategic quality KPI's and performance dashboards to measure effectiveness, efficiency, and customer satisfaction.
• Lead data-driven quality reviews and report critical insights, risk forecasts, and strategic recommendations to executive leadership.

QUALIFICATIONS:

• Graduate of Bachelor's Degree in Engineering (Electrical, Electronics, Mechanical, Industrial, and Computer)
• Minimum of 10 year(s) working experience in related field is required for this position.
• At least 3 year(s) of managing experience in related field is required for this position.
• Strong knowledge in 8D/FMEA/7 QC Tools/SPC.
• Knowledgeable in drawing interpretations to identify the standards given by the customer.
• Relevant trainings and seminars to this position will be of high advantage.
• Willing to be assigned in FPIP Site.

Job Types: Full-time, Permanent

Benefits:

• Company Christmas gift
• Company events
• Staff meals provided
• Transportation service provided

Education:

• Bachelor's (Preferred)

Experience:

• Quality management: 10 years (Required)
• Managing: 3 years (Required)

Language:

• English (Required)

Work Location: In person

JOB SUMMARY:

Provides general direction to the Quality Control Section, which is responsible for standardization, quality assurance of materials and construction, and documentation management. Ensures that all projects and daily operations meet the standard and quality assurance requirements.

QUALIFICATIONS:

• BS Civil / Mechanical Engineering
• Must be a licensed Engineer
• At least three (3) years of relevant work experience
• Knowledgeable in construction quality standards, project audits, materials inspection, and documentation
• Professional certification in quality standards is an advantage
• Must have excellent leadership, decision-making, and communication skills

Job Type: Full-time

Work Location: In person

We are seeking an experienced Quality Assurance & Quality Control (QA/QC) Division Head to lead and oversee quality operations across all aspects of manufacturing, packaging, testing, and compliance. This role is responsible for ensuring that all raw materials, packaging components, in-process and finished products conform to established standards, regulatory requirements, and client specifications.

The QA/QC Head will direct multiple teams engaged in Quality Assurance, Quality Control, Validation, Compliance, and Regulatory activities, while ensuring adherence to cGMP, Good Laboratory Practices, and international quality standards.

Key Responsibilities

• Lead and manage QA/QC teams across multiple sections, including Packaging Inspection, Raw Materials Testing, Microbiological Assay, Physical & Chemical Testing, Stability Studies, Technical Services, Validation, and Regulatory.
• Approve and oversee technical and quality system documents (e.g., manufacturing orders, validation protocols, deviation reports, risk assessments, change control, complaints, CAPA, and SOPs).
• Ensure compliance with FDA, PIC/S, ISO 9001:2015, and other regulatory requirements.
• Conduct audits of suppliers, packaging material vendors, and internal processes.
• Act as lead auditor and approver for suppliers, validation documents, and product release for domestic and international markets.
• Lead investigations, product recalls, and complaint handling, ensuring timely client communication and resolution.
• Provide training, coaching, and performance evaluation for managers and staff under the QA/QC division.
• Oversee GMP training programs, environmental monitoring, equipment validation, and preventive maintenance schedules.
• Collaborate with cross-functional teams including Production, Engineering, Supply Chain, Technical Services, and Accounts Management to drive quality improvements.
• Maintain liaison with FDA and external stakeholders regarding technical and regulatory matters.

Qualifications

• Bachelor's Degree in Chemistry, Chemical Technology, Chemical Engineering, Pharmacy, or Industrial Pharmacy (professional license preferred).
• Minimum of 6 years of managerial experience in QA/QC within the pharmaceutical, cosmetics, veterinary, or food manufacturing industry.
• Strong expertise in GMP, laboratory practices, pharmaceutical manufacturing, packaging technology, and regulatory compliance.
• Hands-on knowledge of validation, risk management, deviation handling, CAPA management, supplier qualification, complaint management, and stability studies.
• Proven leadership skills with the ability to supervise multiple managers and technical staff.
• Strong decision-making, analytical, and problem-solving skills.
• Proficient in project management, report preparation, and technical documentation.
• Computer literate; familiarity with ISO quality systems is an advantage.

Job Types: Full-time, Permanent

Pay: Php250, Php260,000.00 per month

Benefits:

• Company car
• Company Christmas gift
• Company events
• Health insurance
• Life insurance
• Paid training
• Pay raise

Work Location: In person

Company Overview

Established in January 2019, BioAnalytica Inc. is a testing laboratory performing bioanalytical laboratory services to local and international clients dedicated in ensuring quality, safe and reliable drugs for the pharmaceutical industry.

Job description:

· Documentation of the laboratory's quality manual, in accordance to the requirements of ISO/IEC 17025:2017

· Identification, investigation, and resolution of nonconforming work

· Conduct and Participation in internal audits

· Conduct and Participation in management reviews

· Review of Method Validation or Method verification protocol prior to approval and use by the Laboratory.

· Review of Method Validation/Verification reports. Analysis reports, and Certificate of Analysis prior to authorization for release.

· Act as Document controller

· Manages Customer feedback and complaints related to quality and working to resolve issues to enhance customer satisfaction.

Requirements:

· Comprehensive knowledge in ISO/IEC 17025:2017 and OECD Good Laboratory Practices

· Must be a Registered Chemist/Pharmacist with extensive knowledge in HPLC

· At least 1-2 years of experience in Quality Assurance

· Awareness of internal audits as per ISO/IEC 17025:2017 standard, whether participating as an auditor, or an auditee

· Experience in technical documentation, particularly writing procedures, instructions and manuals

Secondary Qualifications:

o Awareness of the ISO/IEC 19011:2018 is a plus

o Awareness on information security

o Knowledge on data privacy as relevant to the data privacy act

o Awareness of ISO/IEC 27001 is a plus

o Awareness of Good Manufacturing Practice is a plus

QUALIFICATIONS:

• Bachelor's Degree in any related field of study General Science, Biology, Chemical Engineering, Engineering, Statistics, Mathematics, or other related courses exposed in Quality Assurance System
• At least 2-5 years proven work experience with Quality Assurance with Managerial status
• Must be Physically Fit

Working Conditions:

• Regular Office Area or assigned on field if needed
• Might deal with chemicals, fumes or airborne particles if needed
• Render extra time if needed

Job Types: Full-time, Permanent

Benefits:

• Opportunities for promotion
• Promotion to permanent employee

Experience:

• QUALITY MANAGEMENT: 1 year (Preferred)

Location:

• General Santos City 9500 P12 (Preferred)

Work Location: In person

Job title
: Training and Quality Director

Location:
Taguig City (Onsite)

Education:
Bachelor's degree in business, Human Resources, Management, or related field.

Experience:
7-10 years of experience in training, quality management, or related fields.

No of Openings:
1

Roles and Responsibilities:

• Develop and Implement Training Programs: Design and roll out effective employee training programs tailored to different departments, ensuring alignment with organizational goals.
• Training Needs Analysis: Collaborate with department heads and HR to identify skills gaps and create targeted training strategies.
• Leadership Development: Implement leadership training programs aimed at developing high-potential employees and future leaders within the organization.
• Quality Standards Development: Establish and enforce company-wide quality standards, ensuring compliance with industry regulations and best practices.
• Quality Audits: Oversee regular audits to evaluate the quality of products, services, and processes across departments.
• Training Evaluation: Continuously monitor and assess the effectiveness of training programs, using metrics such as employee performance, feedback, and productivity.

Required Skills:

• Proven ability to develop and implement training and development strategies.
• Strong knowledge of quality assurance processes and methodologies.
• Excellent leadership and team management skills.
• Exceptional communication, presentation, and interpersonal skills.
• Strong problem-solving and analytical skills.
• Ability to manage multiple projects simultaneously and meet deadlines.
• Bachelor's degree in business, Human Resources, Management, or related field.
• Minimum of 7-10 years of experience in training, quality management, or related fields.
• With at least 5 years in a leadership role in the BPO Industry

II. ROLE AND RESPONSIBILITIES

1. Oversee the overall operation of the Firms' Quality Control System.
2. Recommend new policies and revisions to existing policies for Firm's compliance.
3. Provides guidance and consultation on the application of accounting and auditing standards to Partners and staff.
4. Facilitate and speak in training and seminars on soft and technical skills for the Firm's employees and clients to ensure continuing professional development.
5. Attend and contribute to the meetings of the Philippine Interpretation Committee (PIC).
6. Conduct research works to update the firm on newly issued technical pronouncements, and
7. Review financial statements and audit reports of high-risk audit clients.

III. QUALIFICATIONS: EDUCATION AND EXPERIENCE REQUIREMENTS

A. EDUCATIONAL BACKGROUND

• Bachelor's degree in accountancy
• Must be a CPA, MBA is an advantage

B. EXPERIENCE REQUIREMENTS

• At least 10 years experience in external audit or quality assurance

C. SKILLS AND ABILITIES

i. Technical Skills

• High understanding and application of the Philippine Financial Reporting Standards.
• High understanding and application of the Philippine Standards in Auditing
• High understanding and application of relevant laws and regulations
• High understanding and application of the International Standard on Quality Management (ISQM)

JOB DESCRIPTION:

The Quality Assurance Manager is responsible for the overall quality of operations for the entire company covering the incoming materials, in-process materials and finished goods materials that will be delivered to clients.  He/she must be independent of the other process managers to ensure the unbiased and credible findings that is intended to check, correct and punish non-compliance if necessary to meet the commitment of the company to total quality management.  He/she supervises the Incoming and Data Bank QA Associate and the In-Process and Outgoing QA Inspector.  He/she reports directly to the General Manager and President.

Key Responsibilities:

Monitoring the production processes from pre-press to post-press doing periodic Quality Control checks.

Implementing improvements to the production processes that lead to overall increases in production, service and product quality.

Monitor, report and document all ongoing production processes issues and discuss with Management to find solutions.

Ensure compliance to the Quality Management manual process and requirements.

Assess every stage of production and recommend process improvements necessary.  Investigate causes of quality problems.

Ensure proper and complete documentation of all non-compliance as well as best practices.

Job Requirements:

Successful candidate must be preferably a graduate of Industrial Engineering, or any related course.

to 2 years experience in the areas of quality assurance management and planning is preferred.

Must have strong initiative to review current processes and provide improvement recommendations.

Good organization and time management skills.  Able to multi-task without sacrificing quality and performance objectives.

Advanced computer skills for data management (Microsoft Office – Excel, PowerPoint and Word).

Good interpersonal and communication skills to handle working with production people (plant manager, team leaders, press operators, etc…)