104 Safety Management jobs in the Philippines

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
Why Patients Need You
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.

What You Will Achieve
You will be relied on by the company to monitor its drug, biologics and medical devices surveillance program. This will include intake, evaluation and processing of the adverse reports received. You will support the clinical trial as well as the post marketing activities.

As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.

It is your dedication and hard work that will make it possible for Pfizer's customers and patients to receive the medicines they need, when they need them.

How You Will Achieve It

• Contribute to completion of project milestones and organize own work to meet project task deadlines.

Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission.

Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.

Review case criteria to determine the appropriate workflow for case processing.

Position Purpose
Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer's products and to meet regulatory requirements. Determination of local submission of individual and, where appropriate, aggregate safety reports.

Primary Responsibilities

• Carry out case processing activities.

Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments.

Review case criteria to determine appropriate workflow for case processing.

Assess cases to distinguish those with particular complexities and/or specific issues and escalate appropriately.

Write and edit case narrative.

Determine and perform appropriate case follow-up, including generation of follow-up requests.

Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios.

Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation.

Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database.

Determine reportability of scheduled reports, ensuring adherence to regulatory requirements.

Consistently apply regulatory requirements and Pfizer policies

Participate, as appropriate, in local, internal, and external safety activities

Technical Skill Requirements

• Experience in pharmacovigilance and/or data management preferred

Experience and skill with medical writing an advantage

Demonstrated computer literacy.

Qualifications
Experience in use and management of relational databases preferred

• 1+ years of pharmacovigilance experience preferred

Bachelor's Degree in Health or Life Sciences

Health Care Professional Or Equivalent Experience Preferred.
Ability, with supervision, to solve routine problems and to surface issues constructively.

Ability to make basic decisions with an understanding of the consequences.

Ability to achieve personal objectives while meeting departmental standards of performance.

Ability to work under supervision in a matrix organization.

Fluency in spoken and written English

Physical/Mental Requirements

• Must have the "ability to communicate," "ability to work on teams", "office job involving use of computer", etc.

Work Location Assignment: On Premise (No relocation support)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

Why Patients Need You
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.

What You Will Achieve
You will be relied on by the company to monitor its drug, biologics and medical devices surveillance program. This will include intake, evaluation and processing of the adverse reports received. You will support the clinical trial as well as the post marketing activities.

As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.

It is your dedication and hard work that will make it possible for Pfizer's customers and patients to receive the medicines they need, when they need them.

How You Will Achieve It

• Contribute to completion of project milestones and organize own work to meet project task deadlines.

Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission.

Support Worldwide Strategy and Regulatory teams by providing analyses of post-marketing safety data, reviews of the medical literature, and similar related activities.

Review case criteria to determine the appropriate workflow for case processing.

Position Purpose
Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer's products and to meet regulatory requirements. Determination of local submission of individual and, where appropriate, aggregate safety reports.

Primary Responsibilities

• Carry out case processing activities.

Review, rank, verify, process and document case-related information: event terms; validity, seriousness, special scenarios; timelines; accuracy and consistency. Process cases based on these assessments.

Review case criteria to determine appropriate workflow for case processing.

Assess cases to distinguish those with particular complexities and/or specific issues and escalate appropriately.

Write and edit case narrative.

Determine and perform appropriate case follow-up, including generation of follow-up requests.

Review processed cases to verify accuracy, consistency and compliance with process requirements, and review case data for special scenarios.

Liaise with key partners, locally, and other stakeholders regarding safety data collection and data reconciliation.

Develop and maintain expertise and knowledge for applicable corporate and global regulations, for guidelines, Standard Operating Procedures, for data entry conventions, and for search functions in the safety database.

Determine reportability of scheduled reports, ensuring adherence to regulatory requirements.

Consistently apply regulatory requirements and Pfizer policies

Participate, as appropriate, in local, internal, and external safety activities

Technical Skill Requirements

• Experience in pharmacovigilance and/or data management preferred

Experience and skill with medical writing an advantage

Demonstrated computer literacy.

Qualifications
Experience in use and management of relational databases preferred

• 1+ years of pharmacovigilance experience preferred

Bachelor's Degree in Health or Life Sciences

Health Care Professional Or Equivalent Experience Preferred.
Ability, with supervision, to solve routine problems and to surface issues constructively.

Ability to make basic decisions with an understanding of the consequences.

Ability to achieve personal objectives while meeting departmental standards of performance.

Ability to work under supervision in a matrix organization.

Fluency in spoken and written English

Physical/Mental Requirements

• Must have the "ability to communicate," "ability to work on teams", "office job involving use of computer", etc.

Work Location Assignment: On Premise (No relocation support)

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

Job Description
Pfizer — Safety Data Management Specialist

Location:
Makati City, Metro Manila (Hybrid)

Level:
Junior

Industry:
Pharma, HealthTech, AI, Machine Learning, Biotech

Role Overview

Monitor adverse drug and device reports, support clinical trial and post-marketing safety activities, and ensure compliance with regulatory requirements. Help maintain Pfizer's safety surveillance program by reviewing and processing safety data.

Key Responsibilities

• Process and review adverse event cases for validity, seriousness, and accuracy.
• Write/edit case narratives and perform follow-ups as needed.
• Determine appropriate workflows and escalate complex cases.
• Collaborate with internal teams and external partners on safety data collection and reconciliation.
• Maintain knowledge of regulatory requirements, SOPs, and data entry conventions.
• Determine reportability and ensure compliance with safety reporting regulations.
• Support safety-related activities both locally and globally.

Qualifications & Skills

• Bachelor's degree in Health or Life Sciences.
• 1+ year preferred experience in pharmacovigilance or data management.
• Medical writing skills are a plus.
• Familiarity with relational databases and computer literacy required.
• Ability to solve routine problems with supervision and work effectively in a matrix environment.
• Fluent in English, both spoken and written.

Work Environment

• On-premise role with no relocation support.
• Pfizer is an equal opportunity employer.

Tagged As

• Clinical
• Research
• Biotech
• Healthtech
• Information Technology
• Oncology
• Big Data Analytics
• AdTech
• Digital Media
• Software
• Generative AI

Responsibilities:

• Ensures the completion of documented information review based on timeline as initiated by QMS and Food Safety Officers.
• Consolidates the QD Annual Budget Allocation every last Friday of September for ABP that includes OPEX and CAPEX.
• Ensures the completion of refresher training and alignment of the Integrated Management System standards of all FSQMS Staff on a semi-annual basis with qualifying exams.
• Monitors the completion and or compliance to EMP Program, Pest Control activities, 3rd Party Lab Testing, Cleaning programs, External / Internal Programs, IPM, Document and Records Control and Updating, Retention Evaluation, Food Safety Culture Development Program, GMP / FS Training.
• Ensures the coordination with other departments for the preparation of application requirements for product registration, LTO, and other permits and certificates necessary to ensure on-time application and compliance to statutory and regulatory requirements.
• Monitors current and applicable legislation and government regulations to ensure on-time compliance and implementation based on release / effectivity date.
• Participates in the review of packaging design, revision, and monitoring to ensure compliance on regulatory requirements for labelling.
• Reviews and updates the Site Information File in a timely manner prior to LTO renewal or updates.
• Reviews the effectiveness of the Integrated Pest Management Program by reviewing the performance evaluation on a semi annual basis.
• Reviews the renewal of contracts for third party pest control and cleaning chemicals provider.
• Coordinates the necessary training requirement for the Integrated Pest Management Program.
• Ensures the systematic handling and storage of food safety documented information, of all departments, including management reviews.
• Assists other departments in creating, updating, reviewing of documented information until closure of non-conformances that may impact quality and food safety.
• Handles the scheduled customer visits and audits.
• Consolidates weekly FSQMS report every Monday and sends to R&D, Production Manager, GM and Top Management via email such as but not limited to the following: audit completion, retention evaluation including trials and or modifications.
• Ensures the establishment and review of procedures, responds to all queries on time, and provides assistance to achieve 100% compliance to certification timeline to achieve zero delays.
• Attends NPD meetings and other initiated trials to discuss and align customer requirements and completion of reports respectively.

Qualifications:

• Bachelor's degree in Food Science, Food Technology, Chemistry, or any related field.
• At least 3 to 5 years work experience from any food manufacturing set-up.
• Knowledgeable in ISO / HACCP / GMP / GHP and FDA documentation.
• Can perform quality management system audit

The position is mainly responsible for the development, administration of efficient and professional operations of the company's occupational health and safety(OHS) services in accordance with the company's policies, safety practices and procedures, and applicable government-mandated regulations.

• Safety Programs Administration
• Compliance to OSH Standards
• Occupational Health and Safety Initiatives/ Programs & Process Improvements
• Budget Management for OSH programs & routine activities
• Establishing network/ linkages with government agencies, experts and consultants, government authorities

Job Qualifications:

1. College degree holder, preferably in Nursing or Engineering
2. Must have at least 3 – 5 years direct experience in a supervisory role, handling Occupational Health and Safety
3. Computer literate, technology-savvy
4. Must be an accredited Safety practitioner

The position is mainly responsible for the development, administration of efficient and professional operations of the company's occupational health and safety(OHS) services in accordance with the company's policies, safety practices and procedures, and applicable government-mandated regulations.

• Safety Programs Administration
• Compliance to OSH Standards
• Occupational Health and Safety Initiatives/ Programs & Process Improvements
• Budget Management for OSH programs & routine activities
• Establishing network/ linkages with government agencies, experts and consultants, government authorities

Job Qualifications:

• College degree holder, preferably in Nursing or Engineering
• Must have at least 3 – 5 years direct experience in a supervisory role, handling Occupational Health and Safety
• Computer literate, technology-savvy
• Must be an accredited Safety practitioner

Job Type: Full-time

Benefits:

• Additional leave
• Company Christmas gift
• Company events
• Discounted lunch
• Employee discount
• Free parking
• Health insurance
• Life insurance
• On-site parking
• Paid training
• Pay raise

Application Question(s):

• What's your expected basic monthly rate (please provide exact figure)

Experience:

• Occupational Health & Safety Specialist: 1 year (Required)

Work Location: In person

Opentext - The Information Company
OpenText is a global leader in information management, where innovation, creativity, and collaboration are the key components of our corporate culture. As a member of our team, you will have the opportunity to partner with the most highly regarded companies in the world, tackle complex issues, and contribute to projects that shape the future of digital transformation.

AI-First. Future-Driven. Human-Centered.
At OpenText, AI is at the heart of everything we do—powering innovation, transforming work, and empowering digital knowledge workers. We're hiring talent that AI can't replace to help us shape the future of information management. Join us.

The Opportunity
At OpenText, we put people first. As a Health & Safety Specialist, you will play a key role in supporting the implementation and continuous improvement of Occupational Health and Safety (OHS) programs. Based in our Philippines office, you will provide primary support for OpenText's operations in the Philippines, ensuring compliance with local regulations and promoting a culture of safety. You will also contribute to the development and execution of global OHS programs and initiatives, helping align local practices with international standards. This role is ideal for a developing professional who is eager to grow their expertise, contribute to cross-functional projects, and identify opportunities for continuous improvement. OpenText is more than just a corporation, it's a global community where trust is foundational, the bar is raised, and outcomes are owned. We take pride in the high expectations placed on us by our customers and strive to exceed those expectations with a culture that fosters extraordinary customer service. We are the voice of our customers, and we focus on making them wildly successful.

You Are Great At
Safety Support & Collaboration

• Serve as a key resource for OHS activities and compliance across Philippine operations.
• Support the implementation of safety programs aligned with DOLE regulations and OpenText's global standards.
• Collaborate with internal teams, vendors, and regulators to ensure safe and compliant operations.
• Promote a positive safety culture through awareness campaigns, coaching, and engagement.
• Assist with global and regional environmental programs as directed.

Training & Awareness

• Coordinate and support OHS training sessions, including onboarding and refresher courses.
• Track training completion and maintain accurate records.
• Support behavioral-based safety initiatives and monthly safety committee meetings.

Monitoring & Reporting

• Assist in tracking and reporting OHS performance metrics, including incidents, near misses, and compliance indicators.
• Contribute to data analysis and provide insights to support decision-making and risk mitigation.
• Help prepare reports and documentation for internal and external audits.

Site & Program Support

• Facilitate site inspections, hazard assessments, and risk evaluations.
• Support emergency preparedness and response activities.
• Assist in the development and implementation of site-specific safety procedures and programs.

Compliance & Documentation

• Maintain OHS documentation and ensure alignment with local and international standards.
• Support audits and inspections by DOLE and other regulatory bodies.
• Assist in managing contractor safety programs and ensuring compliance with OpenText's Operational Compliance Program.

Qualifications
What It Takes:

• Bachelor's degree in a related field or equivalent combination of education and experience.
• Minimum of 2 years of relevant experience in occupational health and safety, preferably in a corporate or BPO environment.

Certifications

• Required: Must meet the Department of Labor and Employment (DOLE) qualifications for Safety Officer 3 (SO3), including completion of the Basic Occupational Safety and Health (BOSH) training.
• Preferred: NEBOSH, OHSAS 18001, ISO 9001/14001, and ISO 45001:2018 Implementation and Lead Auditor Training.

Skills & Competencies

• Working knowledge of local and international OHS regulations, including ISO 45001:2018.
• Experience supporting the implementation of safety management systems and compliance programs.
• Strong communication and interpersonal skills to collaborate across teams and with external partners.
• Proficiency in Microsoft Office and digital tools for reporting and training.
• Analytical mindset with attention to detail and a proactive approach to identifying safety improvements.
• Ability to manage multiple tasks and contribute to cross-functional projects in a dynamic environment.

Work Setup

• Hybrid work arrangement: 3 days onsite, 2 days remote.

OpenText's efforts to build an inclusive work environment go beyond simply complying with applicable laws. Our Employment Equity and Diversity Policy provides direction on maintaining a working environment that is inclusive of everyone, regardless of culture, national origin, race, color, gender, gender identification, sexual orientation, family status, age, veteran status, disability, religion, or other basis protected by applicable laws.

If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please contact us at Our proactive approach fosters collaboration, innovation, and personal growth, enriching OpenText's vibrant workplace.

Job Summary

Occupational Health and Safety (OHS) Nurse shall organize and administer occupational health services programs integrating occupational safety to improve and sustain the occupational health and safety management system promoting healthful and safe workplace.

Job Qualifications

• Must be a licensed nurse
• Must have at least experience in a manufacturing firm
• A member of the Occupational Health Nurses Association of the Philippines is preferable
• Must possess a good interpersonal relationship that can adept to different types of personality
• Must be good in both oral and written communications
• Have undergone a course on Basic Occupational Safety & Health
• Can work with minimum supervision and can handle pressure
• Willing to work on night shift

Job Competencies

• Able to communicate to all employees across all levels
• Treat each medical record and other pertinent date of employees with utmost confidentiality
• Able to write and formulate clinic procedure to streamline transactions.

Job Summary

Occupational Health and Safety (OHS) Nurse shall organize and administer occupational health services programs integrating occupational safety to improve and sustain the occupational health and safety management system promoting healthful and safe workplace.

Job Qualifications

• Must be a licensed nurse
• Must have at least experience in a manufacturing firm
• A member of the Occupational Health Nurses Association of the Philippines is preferable
• Must possess a good interpersonal relationship that can adept to different types of personality
• Must be good in both oral and written communications
• Have undergone a course on Basic Occupational Safety & Health
• Can work with minimum supervision and can handle pressure
• Willing to work on night shift

Job Competencies

• Able to communicate to all employees across all levels
• Treat each medical record and other pertinent date of employees with utmost confidentiality
• Able to write and formulate clinic procedure to streamline transactions.

Job Types: Full-time, Fresh graduate

Benefits:

• Additional leave
• Company Christmas gift
• Discounted lunch
• Employee discount
• Free parking
• Health insurance
• On-site parking
• Opportunities for promotion
• Paid training
• Pay raise

Work Location: In person