739 Senior 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

Duties and Responsibilities:

• Strongly enforce project safety rules and policies
• Implement and maintain health and safety standard
• Can do safety documentation and record keeping
• With valid first aid certificate and do health program
• Can do incident/accident investigation report

Qualifications:

• Graduate of any 4 year course
• With at least 5 years relevant experience in a construction industry
• With BOSH Training
• OSH Practitioner

Job Type: Full-time

Benefits:

• Health insurance
• Life insurance

Work Location: In person

What you'll be doing

• Ensure compliance with Occupational Health and Safety (OHS) guidelines
• Conducting regular site inspections and risk assessments to identify and mitigate potential safety hazards
• Implementing and enforcing safety policies, procedures and best practices across project sites
• Providing safety training and toolbox talks to educate workers on safe work practices
• Investigating and reporting on all incidents, accidents and near-misses, and implementing corrective actions
• Maintaining detailed records and documentation related to safety management
• Help management ensure employees follow safety and health rules
• Take charge during emergencies and crises

What we're looking for

• Minimum 5 years of experience as a Safety Officer in the construction industry
• Strong knowledge of health, safety and environmental regulations, standards and best practices
• Excellent communication and interpersonal skills to engage with workers at all levels
• Proactive problem-solving abilities
• Proficiency in computer and Microsoft Office
• Certification in occupational health and safety, such as NEBOSH or OSH, is preferred

If you are a motivated and safety-focused professional looking to join a dynamic team, we encourage you to apply now.

Jane Town Recruitment Services on behalf of Confidential is hiring a Full time Safety Officer role in Tanauan, Calabarzon. Apply now to be part of our team.

Job summary:

• Looking for candidates available to work:
• Monday: Morning
• Tuesday: Morning
• Wednesday: Morning
• Thursday: Morning
• Friday: Morning
• Saturday: Morning
• 1 year of relevant work experience required for this role

We're in urgent need of EHS Staff (Safety Officer III) for a well established Japanese Manufacturing Company located in Sto. Tomas, Batangas. This opportunity is for Direct Hire, send us your applications now and we'll be in touch shortly.

Qualifications:

• Bachelor's Degree Graduate
• Completed a 40-hour Occupational Safety and Health (OSH) training course
• Completed an additional 48 hours of advanced or specialized OSH training
• Have at least (2) two years of relevant OSH experience
• Must have valid BOSH SO3 Certificate / LCM Certificate
• Willing to work in FPIP, Sto. Tomas, Batangas
• Preferably someone who can start ASAP

Come aboard so we can Build a Brilliant Future Together

Meralco is more than a power distribution company. It is home to those who value innovation, dynamism, as well as development of one's self and well-being. Meralco wholeheartedly believes in the significance of customer service, performance, accountability, integrity, and teamwork. Mayroong tunay na malasakit sa kapwa at sa bayan.

Meralco brings out the best in people by championing innovative solutions that move everyone towards a promising future together – for its employees, customers, community and country.

Join us at Meralco and experience a brilliant life.

Meralco. Ang Liwanag ng Bukas.

JOB SUMMARY

• The Safety Officer is responsible for ensuring the overall safety, health, and environmental compliance within the organization. This role conducts regular safety inspections to ensure adherence to all relevant regulations. Promotes a proactive safety culture by identifying and mitigating risks and ensuring a safe and secure work environment for all employees.

GENERAL RESPONSIBILITIES

• Conducts regular spot field inspections and safety audits to identify potential hazards and ensure compliance with safety regulations and company policies; observes work methods and procedures of workers to determine unsafe working conditions and practices.
• Creates Initial / Final Incident Investigation Reports for medical treatment cases or lost-time incidents (including creation of Safety Alerts).
• Oversees safety protocols and risk assessments for company events, ensuring all activities comply with health and safety standards to protect employees and guests.
• Prepares and submits accurate and timely reports to ensure that all required documentations are complete and compliant to the labor and safety laws.
• Observes and complies with existing company codes, policies, agreements, rules and regulations.

QUALIFICATIONS

• Must be a Registered Electrical Engineer or a Registered Master Electrician
• Fulfilled the requirements for Safety Officer 2
• Preferably with at least 2 years in BBS, safety leadership, or safety culture programs
• Knowledgeable with Occupational Safety and Health Standards
• Completed the training course on BOSH/COSH (Basic Occupational Safety & Health / Construction Occupational Safety & Health)
• Amenable for a project-hire contract for 3 years
• Must have a valid driver's license for a 4-wheel manual transmission
• Willing to work onsite (Ortigas, Pasig)

OUR VALUES

• Excellence
• Customer Centricity
• Sustainability
• Integrity
• Innovation
• Malasakit
• Bayanihan

If these things align to your personal values, please don't hesitate to apply. Join us at Meralco and experience a brilliant life.

Job description:

• Graduate of any 4 years course
• With BOSH and LCM at minimum
• With at least 2 years experienced in Heavy Equipment Operation and Material Handling/Transportation

Job Type: Full-time

Benefits:

• Health insurance
• Life insurance

Work Location: In person

Qualifications (Required):

• DOLE-certified Safety Officer 2 (SO2).
• Construction Occupational Safety and Health (COSH) Training Certificate.

Responsibilities:

• Submits all required health and safety statutory and regulatory reports in compliance with legal requirements.
• Plans, implements, and monitors OHS policies and programs to achieve zero disabling accidents and fatalities.
• Conducts risk assessments for critical processes, especially during major concreting and structural activities.
• Investigates accidents/incidents and submits detailed reports with root cause analyses to management.
• Recommends and/or conducts health and safety training for employees and safety orientations for subcontractors.
• Represents the company in safety and health associations, meetings, conferences, and conventions.
• Provides OSH technical consultancy services to management and project teams.
• Conducts regular safety inspections, audits, and risk assessments at project sites; recommends and enforces corrective actions.
• Ensures effective communication and coordination with Project Managers, Site Engineers, staff, clients, and subcontractors regarding safety protocols and hazard mitigation.

Preferred / Advantageous:

• DOLE-certified Safety Officer 3 (SO3).
• Working at Heights Training Certificate.
• Scaffold Safety Training Certificate (especially for overseeing scaffolding operations).