330 Site Supervision 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

Benefits

• Competitive compensation package
• Performance-based cash incentives
• Performance-based salary increase
• Employee discounts and gift certificates
• HMO for employee and dependents
• Above standard leave credits (including birthday leave)
• Employee engagement events and activities
• Monday to Friday workweek
• Terms and conditions apply

Responsibilities

• Perform in-process, incoming, and final inspections of materials and finished products.
• Conduct quality tests using various instruments, equipment, or lab procedures depending on the product type.
• Document and report non-conformances, and follow up on corrective and preventive actions (CAPA).
• Maintain and calibrate testing equipment and ensure its proper functioning.
• Prepare and maintain QC documentation including test reports, checklists, certificates, and logs.

Qualifications

• Diploma or Bachelor's degree in Science, Engineering, Food Technology, or related field.
• 2–5 years of experience in quality control or quality assurance role.
• Knowledge of testing procedures, sampling methods, and quality systems.
• Familiarity with regulatory standards (ISO 9001, GMP, FDA).
• Strong attention to detail and documentation skills.

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Job Type: Full-time

Job Type: Full-time

Work Location: In person

JOB DESCRIPTION:

• Examine products for defects and test functionality
• Observe and evaluate manufacturing and operational processes
• Record and analyze inspection results

QUALIFICATION:

• At least High School/Senior High School graduate
• With related experience as Quality Control/Quality Assurance
• With available basic requirements (SSS, Philhealth, Pagibig, TIN)
• Willing to start ASAP

LOCATION: Mawaque Road, Mabalacat, Pampanga

• Inspections & Testing:

• Product Evaluation: Conduct inspections and testing of raw materials, in-process products, and finished goods.

• Sensory Evaluation: Perform checks on taste, smell, texture, and appearance to ensure products meet benchmarks.
• Lab Analysis: Collect samples for microbiological, chemical, and physical testing (e.g., pH, moisture, contaminants).

• Documentation & Reporting:

• Record Keeping: Maintain detailed and accurate records of all quality control activities, test results, and deviations for traceability.

• Reporting: Document findings, identify non-conformances, and make recommendations for quality improvement to management.

• Compliance & Monitoring:

• Regulatory Adherence: Ensure compliance with food safety regulations, such as those from health and safety organizations, and company policies.

• Process Monitoring: Monitor and verify critical control points (CCPs) in the production process to prevent hazards.
• Hygiene & Sanitation: Inspect facilities and equipment to ensure proper hygiene and sanitation practices are followed.

• Problem-Solving & Improvement:

• Issue Resolution: Investigate and resolve quality-related issues and customer complaints.

• Corrective Actions: Collaborate with production teams to identify root causes of quality issues and implement corrective and preventative actions.

• Supplier & Internal Collaboration:

• Supplier Relations: Coordinate with suppliers to ensure the quality of incoming raw materials.

• Teamwork: Work closely with production, research and development (R&D) teams, and management to maintain and improve product quality.

Job Summary

The QC Lab Analyst Associate is responsible for conducting routine and non-routine laboratory analyses on raw materials, in-process samples, and finished products to ensure compliance with quality standards and regulatory requirements. This role supports the QC team in maintaining the accuracy, reliability, and integrity of laboratory data.

Key Responsibilities

RM Receiving:

• Analyzes all incoming raw material deliveries; determines acceptance and rejection status.
• Inform Purchasing and SCM personnel about any quality issues regarding incoming packaging and raw materials

FG Analysis

• Analyzes all finished products for load-out; releases, rejects, and holds depending on the status of analysis
• Inform Production and Formulation and Research for any quality issues on products.

Inter-department collaboration:

• Analyse sample requests from other departments and company's personnel.

Laboratory innovation:

• Develop new analytical methods and updates laboratory test procedures.

Good Laboratory Practice:

• Maintains laboratory equipment's.
• Closely monitors laboratory supplies inventory and acquisition of chemicals.

Regulatory Compliance:

• Certifies product or raw material chemical analysis (chemist for physical and chemical analyzes) another test for non-chemist).

Others:

• Discuss laboratory functions and activities during mill tours from existing and non-company customers.
• Performs other tasks as may be assigned by immediate superior.

QUALIFICATIONS:

• Preferably BS Chemistry / Chemical Engineering /Food Technology and other science courses with valid PRC License as Chemist / Chemical Technician.
• Experience in operating basic laboratory equipment
• Experience in conducting basic analysis for Feed (Proximate and Mineral Analysis
• Experience in Feed Mill Industry processes
• Experience in Handling Customer Complaints
• Knowledgeable in Good Laboratory Practices
• Knowledgeable in Quality Management System
• Knowledgeable in Regulatory Compliance
• Computer literate (MS Word, Excel, PowerPoint)
• Excellent communication skills, both oral and written.

Job Types: Full-time, Permanent

Benefits:

• Company Christmas gift
• Company events
• Health insurance
• Life insurance
• Opportunities for promotion
• Promotion to permanent employee
• Staff meals provided

Work Location: In person

Position Summary

The Quality Control (QC) Officer is responsible for monitoring and inspecting project activities to make sure all works meet the required quality standards, project specifications, and sustainability requirements such as LEED Certification. The role includes inspections, testing, documentation, and coordination with the project team to ensure proper implementation.

Key Responsibilities

• Inspect and monitor materials, equipment, and work to ensure compliance with approved plans, standards, and LEED requirements.
• Check construction materials to confirm they are approved and meet sustainability guidelines (e.g., low-VOC paints, certified wood, recyclable materials).
• Record inspections, test results, and prepare reports for submission and documentation.
• Coordinate with engineers, supervisors, and workers to resolve quality issues.
• Support waste management, indoor air quality checks, and other LEED-related site activities.
• Assist in implementing quality procedures, safety guidelines, and environmental standards.
• Participate in final inspections, testing, and commissioning before project handover.

Qualifications

• Graduate of Civil Engineering, Mechanical Engineering, Industrial Engineering, or related field.
• With 1 to 2 years of experience.
• Knowledge or familiarity with LEED requirements is an advantage.
• Detail-oriented, organized, and willing to learn.
• Good communication skills and ability to work in a team.
• Willing to be assigned in Hermosa, Bataan.

Job Type: Full-time

Work Location: In person

Application Deadline: 09/26/2025

Expected Start Date: 09/29/2025

Quality Control & Assurance

• Inspect incoming raw materials and packaging for quality and specifications.

• Perform in-process and finished-goods checks (weight, color, viscosity, pH, microbial testing as needed).

• Approve or reject batches and maintain release records.

Documentation & Compliance

• Maintain complete and accurate batch manufacturing records, QC logs, and Certificates of Analysis.

• Ensure compliance with FDA and Good Manufacturing Practices (GMP).

• Prepare and organize documentation for FDA inspections and audits.

Inventory & Materials Control

• Maintain real-time inventory of raw materials and packaging.

• Track and reconcile all incoming and outgoing finished goods using FIFO/FEFO practices.

• Generate monthly inventory reports and alert management on re-order needs.

Lab Organization & Sanitation

• Enforce daily and weekly cleaning schedules for equipment and workspace.

• Ensure proper storage, labeling, and placement of raw materials and finished products.

• Oversee adherence to all SOPs during mixing and production.

MAJOR FUNCTION:

• Supervises the personnel to produce good-quality products as required by company set qualifications.
  
  •  Accomplishes manufacturing results by communicating daily production activities.
  
  • Helps the department head by monitoring progress, resolving problems, and reporting results to management.
  
  •  Links the quality and production principles and ensures that they meet all company-set specifications.
  
  •  Ensures operations are not idled by calling for repairs, material requisitions, and purchasing.
  
  •  Provides manufacturing information by compiling, sorting, and analyzing production performance 
  
  •  Ensures that raw materials and packaging materials are used properly.
  
  •  Monitors personnel's day-to-day work routines
  
  •  Collects batch numbers per product batch to ensure the right labels are on products as required in Good Manufacturing Principles.
  
  •  Monitor daily production activities like bulk oil, shortening, and margarine storage.
  
  •  Assist in bulk oil tank withdrawals.
  
  •  Checks water samples for potable water for consumption.
  
  •  Lobby production and quality-related concerns to the Quality Assurance Department
  
  •  Check personnel's hygiene routine as required in Good Manufacturing Practices.
  
  •  Strictly monitors area cleanliness and raw and packaging material usage.

QUALIFICATIONS:

• Relevant degree such as bachelor's degree in Industrial Engineering
  
  •  May include education, certification, and experience as advantage.
  
  •  Must have a strong knowledge and background on Food Quality Standards and Safety & Health Regulations.
  
  •  Strong decision-making skills and a result-driven approach
  
  •  Has good communication and interpersonal skills