7 Pollution Control Officer jobs in the Philippines

1. Responsible for planning, organizing, and directing the completion of specific ESH projects while ensuring these projects are on time, on budget, and within scope. 2. Oversee projects from inception to completion with the end in mine in, helping to reduce costs, maximize company efficiencies, and increase revenue. 3. Define the main objectives of the project, its purpose, and its scope. Discuss shared expectations, and gain the required authorization from TOP management to move a project forward. 4. The plan established during this process helps project managers oversee scope, cost, timelines, risk, quality issues, and communications. It is during this phase that project managers will outline key deliverables and milestones and identify the tasks that must be completed to complete each. 5. Identify key lessons learned after a project has been completed. Understanding on what went well, what could be done differently and future improve project management practices in the future. 6. Perform audits in ESH areas of concerns. Identify these risks and how to mitigate them, and determine environmental impacts. 7. Knowledgeable in waste water treatmentRequirements1. With 3-5 years' experience as an ESH Engineer in an FMCG manufacturing plant.2. Has handled multiple ESH projects in previous company. 3. Must be an Engineering graduate (IE, ME and Che). 4. Knowledgeable in applicable laws and regulatory requirements related to ESH

QUALIFICATIONS:

- Graduated Bachelor's Degree in Engineering./ Industrial / Nursing or equivalent
- Must possess valid BOSH Training Certification for SO2 / SO3
- Must possess valid Certification as Pollution Control Officer
- With at least 2 years of relevant experience as Safety Officer in manufacturing industry
- Knowledge in Safety Regulations and Compliances, Risk-Based Assessment of Hazards in the Workplace and Aspect-Impact Assessment.
- Trained in Management System is an Advantage.
- Willing to be assigned at Meycauayan City, Bulacan
- Can start ASAP

MAIN RESPONSIBILITY:
Responsible in planning, organizing, developing, implementing, controlling and promoting activities and programs of Environmental, Occupational Health and Safety to ensure the safety of life and property within the organization.

DUTIES AND RESPONSIBILITIES:

- Assist in compliance, review, general risk assessment and other safety assessments to support health, safety and Environment Management.
- Maintain relevant HSE log and documentation & Prepare applicable HSE report as necessary
- Assist in the compliance of applicable laws and regulation
- Provide assistance and advice on HSE issues to make recommendation to facility management
- Participate in detailed incident investigation and root cause analysis & Promote incident prevention for the benefit of employees and visitors
- Assist in the development and presentation of relevant HSE training & Comply with company and HSE procedures and policies
- Observe HSE regulations, wear all required safety equipment, encourages safe working practices, correct obvious hazard immediately or reports them to the proper personnel
- Ability to work with employees and achieve cultural change in the face of potential resistance
- Maintain positive and proactive relation with manager and employees as well as customers and regulatory agencies
- Perform other work related tasks as required
- Walk the manufacturing floor on a regular basis to establish HSE presence and provide support
- Conduct daily and monthly HSE meeting / training and schedule needed & Perform facility HSE inspection
- Write implement and manage HSE Programs, Policies and procedures
- Ability to evaluate PPE and ensure proper use and maintenance of PPE
- Have knowledge and enforce compliance of Regulatory requirements including company HSE policies and procedures
- Ability to Oversea Hazardous Waste storage and endure regulatory agency compliance
- Assist emergency response and provide First Aid treatment
- Follow fall Protection program, inspect all fall protection
- Plan and Oversee Vehicle Maintenance and Safety

Great benefits await you!
- w/ HMO
- w/ Accident Insurance
- w/ Life Insurance
- w/ Free Uniform
- w/ Rice allowance

**Benefits**:

- Company Christmas gift
- Company events
- Free parking
- Health insurance
- Life insurance
- On-site parking
- Paid training
- Pay raise
- Promotion to permanent employee

Schedule:

- 8 hour shift

Supplemental Pay:

- 13th month salary
- Performance bonus

Ability to commute/relocate:

- Meycauayan, Bulacan: Reliably commute or planning to relocate before starting work (preferred)

**Duties and Responsibilities**:
Assist with the renewal of Product Registration and Licenses.

Assistant to the MRA Department

Assist on product label review, dossier review, promo materials and editing.

Administrative responsibilities, product filing in server, scanning of documents, filing of hard copies.

**Qualifications**:

- Graduate of Bachelor of Science in Pharmacy. With or without license.
- Willing to be assigned in Rockwell Makati
- Can work independently with less supervision
- Available to start anytime
- Fresh graduates are welcome.

**Job Type**: Temporary
Contract length: 12 months

**Benefits**:

- Flextime

Schedule:

- Day shift

Supplemental Pay:

- 13th month salary
- Overtime pay
- Yearly bonus

COVID-19 considerations:
All employees and visitors are required to wear mask, self declare and take temperature

Ability to commute/relocate:

- Makati City: Reliably commute or planning to relocate before starting work (required)

**Objective of the position**:

- To deliver Product Safety Service tasks to safeguard compliance to Philippine legislations and company directives to ensure business continuity and operations of businesses under care of Philippine Product Safety.

**Main Areas of Responsibilities**:

- Manage Regulatory Operations and Compliance Services
- Plan and align registration strategy with stakeholders by providing wholistic view of the requirement including data gap assessment and advise alternative approach to be able to agree on realistic timeline
- Develop and implement documented regulatory end-to-end process to establish efficient and systematic work structure.
- Champion Product Stewardship
- Implement applicable regulatory conditions such as but not limited to country label requirement; post notification requirements, post registration requirements and reporting requirements through engagement with internal stakeholders and functional supports to achieve full regulatory compliance
- Assist in regulatory monitoring focusing on area of specialization. Work with Product Safety Country Expert and relevant Operational Divisions in analysis and impact assessment for a provision of Management of Change.
- Drive regulatory advocacy with alignment to corporate BASF positions as appropriate in the local context through engagement with local industry associations and participation in relevant activities capacity building, workshops, etc.
- Provide periodic training and professional advice to stakeholders under area of specialization to ensure dissemination of updated information
- Data Gate Keeper
- Establish, manage, and maintain central documentation of submissions and relevant correspondence with authorities ensuring implementation of proper controls in CBI handling.
- Ensure appropriate and updated maintenance of country monitoring database and /or Operational Division Registration Database to provide visible status to stakeholders
- Ensure initiation of BASF Reference & Real Substances Data maintenance according to NSN to warrant appropriate country regulatory status in BASIS.

**Minimum Qualifications**:

- Bachelor’s Degree in Pharmacy with valid professional license. FDA Qualified Person in Industry Regulatory Affairs accreditation is an advantage.
- With 3-5 years of work experience in chemical or allied industry dealing with quality management or regulatory affairs. Experience in multi-national companies or large local companies with matrix organizational setup is preferred.
- Knowledgeable of organic and inorganic chemistry, polymer chemistry; analytical chemistry and quantitative analysis.
- Possess basic to in-depth knowledge of Philippine Chemical Legislations.
- With good analytical and problem-solving skills.
- Possess good organizational skills, a proactive mindset, and ability to multitask and prioritize work.
- Express self well in English both orally and in writing.
- Proficient in Windows and MS Office Applications.
- Demonstrate leadership, professionalism, and integrity at work.

WHAT YOU WILL DO:

- Regulatory Affairs Assistant will encode the Information on the Drug Package Insert in the POS Plus database template.
- Regulatory Affairs Assistant will verify existing Gamot Guide and Medical Information data existing in the POS Plus system.
- Regulatory Affairs Assistant will assist Regulatory Affairs Officers in the clean up of Regulatory Affairs Database system.

TO BE SUCCESSFUL IN THIS ROLE YOU MUST HAVE:

- Bachelors / College Degree in Pharmacy/Registered Licensed Pharmacist
- Fresh graduate / 1 year experience

**Job Type**: Part-time
Contract length: 5 months

Schedule:

- 8 hour shift

Ability to commute/relocate:

- Parañaque City: Reliably commute or planning to relocate before starting work (preferred)

**Education**:

- Bachelor's (preferred)

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
**Responsibilities may include the following and other duties may be assigned.**
+ Execute submission strategy on-time
+ Prepare dossier for regulatory submissions for Global Region
+ Liaise with Operating Unit regulatory affairs and stakeholders to ensure alignment on submission plan
+ Notify manager in a timely manner upon recognition of issues
+ Respond to queries from FDA/MoH
+ Keeps abreast of regulatory procedures and changes.
+ Provide on-time status about projects under their scope and all applicable regulatory activities assigned
**Required Knowledge and Experience**
+ Bachelor's Degree in Pharmaceutical Sciences, Industrial Engineering, Biomedical Engineering,
+ or field related experience.
+ At least 1-year regulatory experience in medical devices
+ Experience in document interpretation, queries and workflow skills is an advantage
+ Proficiency in Microsoft tools
+ Excellent communication skills
+ Ability to work as part of a team, good analytical and problem-solving skills
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email