388 Site Supervision 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

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

• 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.

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

Job Qualifications:

• Must be a graduate of Bachelor of Science in Industrial Engineering.
• Computer Literate.
• Preferably with experience in the same field in a Rubber Industry.

Job Responsibilities:

• Will be in-charge at quality for 2nd Process.
• Conduct verification of quality of products and evaluates the results.
• Responsible in the identification of abnormal condition, its changepoints and ensures implementation of the corresponding controls.
• Promote "early detection" of quality of all QC process.
• Promote continuous improvement through Kaizen ideas specifically in productivity improvement.
• Genba checking to check compliance to the procedures/rules.

Job Type: Full-time

Benefits:

• Company events
• Free parking
• Transportation service provided

Work Location: In person

JOB QUALIFICATIONS:

• Must be a graduate of BS in Food Technology, Chemistry, Chemical Engineering, or a related field.
• At least 1 year of work experience in a related field is required, preferably within the manufacturing or production industry, with exposure to food processing and food packaging considered an advantage.
• Fresh graduates are encouraged to apply.
• Willingness to work or relocate to the Navotas, CAMANAVA area is required.

Duties and Responsibilities:

• Ensure consistent quality of products throughout all stages of production.
• Conduct audits to verify compliance with quality standards on the production line, ensuring adherence to food safety regulations and requirements.
• Knowledge of food safety, Halal certification, ISO standards, or FDA regulations is a plus.
• Develop standard operating procedures (SOPs) that align with Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMPs).
• Monitor consistency of raw materials, including aging and expiration dates. Collect daily production samples for aging tests and water activity analysis.
• Conduct in-house laboratory tests, including pH, moisture content, viscosity, fineness, texture analysis, total solids, and similar parameters.

Job Types: Full-time, Permanent

Pay: Php18, Php23,000.00 per month

Benefits:

• Additional leave

Work Location: In person