907 Senior Safety Management jobs in the Philippines

Job Summary

Trainovate Inc. is seeking a Marine Safety Management Training Instructor to deliver high-quality training programs focused on maritime safety, risk management, and regulatory compliance. The role involves developing course materials, conducting engaging sessions for corporate and industry clients, and ensuring all programs align with international and local maritime standards such as ISM Code, MARPOL, SOLAS, and STCW.

Key Responsibilities

• Conduct training programs on Marine Safety Management Systems (SMS), ISM Code, and other maritime safety topics.
• Develop, update, and customize course materials to meet client and regulatory requirements.
• Ensure compliance with IMO, MARINA, and DOTr standards in all training content.
• Facilitate engaging and interactive sessions using real-world case studies and simulations.
• Evaluate participants' learning progress and provide constructive feedback.
• Coordinate with the training operations team for course scheduling and logistics.
• Provide professional advice to clients on safety management, compliance, and risk reduction.
• Maintain accurate training records, documentation, and reports.
• Participate in internal quality assurance and course audits for continuous improvement.
• Stay updated on current maritime safety regulations and best practices.

Qualifications

• Bachelor's Degree in Marine Transportation, Marine Engineering, or a related field.
• Licensed Marine Officer (Deck or Engine) or equivalent maritime safety background preferred.
• Minimum 3–5 years of relevant experience in shipboard operations, marine safety, or safety management systems.
• Strong knowledge of ISM Code, SOLAS, MARPOL, and STCW standards.
• Experience in corporate or technical training delivery is an advantage.
• Excellent communication, presentation, and interpersonal skills.
• Proficient in MS Office and e-learning tools; experience in digital or blended training preferred.
• With Trainer's Methodology (TM I or II) or equivalent certification is a plus.
• Willing to travel for on-site corporate training engagements.

Why Join Us?

• Opportunity to work with leading corporate and maritime industry clients.
• Dynamic and collaborative training environment.
• Competitive compensation and project-based incentives.
• Professional growth and development opportunities.

Job Type: Part-time

Benefits:

• Flexible schedule

Experience:

• relevant industry: 3 years (Required)

License/Certification:

• Marine Officer Certificate (Deck or Engine) (Required)

Work Location: In person

Qualifications:

• Graduate of any four year course, preferably engineering.
• With good oral & written communication skills, analytical and organizational skills.
• Computer Literate: Proficient in using Microsoft Office Applications.
• High Consideration to details.
• With exposure in Auditing is an advantage.

Job Type: Full-time

Pay: From Php700.00 per day

Benefits:

• Company Christmas gift
• Company events
• Employee discount
• Opportunities for promotion
• Paid training

Education:

• Bachelor's (Required)

Work Location: In person

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

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

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

JOB SUMMARY: (In a few lines, describe the over-all job or function of the position)

We are looking for a Safety Officer who's willing to be assigned in Mabalacat Pampanga.

The Safety Officer plays a critical role in ensuring the safety and well-being of personnel, equipment, and the environment at the project site. Reporting to the Project Manager, the Safety Officer is responsible for implementing and enforcing safety policies, procedures, and regulations to prevent accidents, injuries, and hazards. They collaborate with project teams, subcontractors, and stakeholders to promote a culture of safety and compliance with safety standards and best practices.

DUTY (Critical/key obligation to perform)

SAFETY POLICY IMPLEMENTATION:

· Implement and enforce safety policies, procedures, and regulations to ensure compliance with legal requirements and industry standards.

· Develop and communicate site-specific safety plans, protocols, and emergency procedures to project teams, subcontractors, and personnel.

SAFETY INSPECTION AND AUDITS:

· Conduct regular safety inspections, audits, and risk assessments to identify potential hazards, unsafe conditions, and safety violations.

· Prepare inspection reports, document findings, and recommend corrective actions to mitigate risks and improve safety performance.

SAFETY TRAINING AND EDUCATION:

· Provide safety training, orientation, and awareness programs for project personnel, subcontractors, and new hires.

· Facilitate toolbox talks, safety meetings, and educational sessions to promote safety awareness and best practices on site.

INCIDENT INVESTIGATION AND REPORTING:

· Investigate accidents, incidents, and near misses to determine root causes, contributing factors, and lessons learned.

· Prepare incident reports, document findings, and recommend corrective actions to prevent recurrence and improve safety performance.

SAFETY COMMUNICATION AND COLLABORATION:

· Communicate safety policies, procedures, and initiatives to project teams, subcontractors, and stakeholders to promote understanding and compliance.

· Collaborate with project teams to integrate safety requirements into project planning, scheduling, and execution.

SAFETY COMPLIANCE MONITORING:

· Monitor and enforce compliance with safety regulations, standards, and best practices by conducting site inspections and audits.

· Review and evaluate subcontractor safety programs, practices, and performance to ensure alignment with project safety requirements.

EMERGENCY RESPONSE AND PREPAREDNESS:

· Coordinate emergency response activities and drills to ensure preparedness for potential emergencies, such as fires, accidents, or natural disasters.

· Establish communication protocols, evacuation procedures, and emergency response plans to minimize risks and protect personnel.

PROFILE OF JOB / POSITION HOLDER

EDUCATIONAL ATTAINMENT:

· Bachelor's degree in occupational health and safety, Environmental Science, Industrial Engineering, or a related field is preferred. Equivalent work experience in occupational safety may be considered in lieu of a degree.

CERTIFICATIONS:

· Certification in Occupational Health and Safety (e.g., OSHA 30-hour General Industry) is highly desirable.

EXPERIENCE:

· Minimum of 3 years of experience in a safety-related role, preferably in a manufacturing, construction, or industrial setting.

· Experience conducting safety inspections, audits, and incident investigations.

COMMUNICATION SKILLS:

· Excellent verbal and written communication skills with the ability to effectively communicate safety policies, procedures, and training materials.

· Strong interpersonal skills to interact with project-based employees at all levels of the organization, as well as regulatory agencies and external stakeholders.

ANALYTICAL SKILLS:

· Strong analytical and problem-solving skills to identify safety hazards, assess risks, and develop effective control measures.

· Ability to analyze incident data and trends to proactively address potential safety issues.

LEADERSHIP ABILITIES:

· Demonstrated leadership qualities with the ability to influence and motivate others to prioritize safety.

· Proven track record of implementing safety initiatives and driving continuous improvement in safety performance.

ATTENTION TO DETAILS:

· Attention to detail and accuracy in conducting safety inspections, documenting findings, and maintaining records.

· Ability to review safety procedures and protocols for completeness and effectiveness.

REGULATORY KNOWLEDGE:

· Comprehensive understanding of federal, state, and local safety regulations applicable to the industry.

· Ability to interpret and apply regulatory requirements to ensure compliance and mitigate risks.

TEAM COLLABORATION:

· Ability to work collaboratively with cross-functional teams to address safety concerns and implement solutions.

· A willingness to listen to feedback from employees and incorporate their input into safety programs and initiatives.

EMERGENCY RESPONSE SKILLS:

· Knowledge of emergency response procedures and protocols, including fire safety, evacuation plans, and first aid/CPR.

· Experience coordinating emergency drills and exercises to ensure preparedness.

CONTINUOUS LEARNING:

· Commitment to staying updated on emerging trends, best practices, and advancements in occupational health and safety.

· Willingness to pursue additional training and certifications to enhance professional development.

Job Type: Full-time

Pay: Php18, Php25,000.00 per month

Benefits:

• Company Christmas gift
• Company events
• Flexible schedule

Willingness to travel:

• 50% (Preferred)

Work Location: In person

At Least High School Graduate Als Graduate Senior High School Graduate or College Under Graduate open to Apply with or Without Experience w/ (COSH) SO2

Job Type: Full-time

Pay: Php18, Php19,000.00 per month

Work Location: In person

MEDAVIS, INC. is hiring a Full time Safety Officer role in Muntinlupa, NCR. Apply now to be part of our team.

Job summary:

• Flexible hours available

Requirements

• Graduate of at least Vocational Course
• With Construction Occupational Safety & Health Certificate (COSH)
• Good knowledge in construction safety
• Preferably with experience as Safety Officer
• Willing to be assigned in any project site
• Can start immediately
• With complete requirements

• Develops, implements, and enforces health and safety policies, procedures, and protocols in compliance with local and national regulations.
• Conducts regular inspections and risk assessments to identify potential hazards in the kitchen, dining, storage, and food preparation areas (HIRADC, JHA, Work Methodology).
• Monitors compliance with food safety standards, including HACCP, GMP, and sanitation requirements.
• Investigates accidents, incidents, and near-misses; prepares reports and recommends corrective/preventive actions.
• Filing and documentation of accident and illness for DOLE compliance.
• Conducts safety training and orientation sessions for new and existing staff on topics such as proper food handling, emergency procedures (fire and earthquake drill) and use of personal protective equipment (PPE), 8hrs mandatory BOSH Training.
• Ensures all safety equipment (e.g., fire extinguishers, first aid kits, signage) is maintained and accessible.
• Coordinates with local health authorities and regulatory bodies during inspections and audits.
• Maintains up-to-date safety documentation and records, including incident logs, inspection reports, and training records.
• Leads or participates in safety committee meetings and emergency drills.
• Promotes a proactive safety culture and continuous improvement in safety performance across the organization.

Qualifications:

• 40 hrs. Training of Occupational Safety and Health, With SO2 certificate.
• HACCP, or other safety-related credentials is an advantage.
• At least 2-3 years of relevant experience as Safety Officer in related field.
• Knowledge in local labor (DOLE) and food safety laws and regulations.
• Familiarity with safety inspection tools and techniques.
• Strong attention to detail, critical thinking, and problem-solving skills.
• Good communication and interpersonal skills; able to train and influence staff at all levels.
• Proficient in report writing and documentation.

Job Types: Full-time, Permanent

Pay: Php15, Php20,000.00 per month

Benefits:

• Employee discount
• Paid training

Work Location: In person