10 Pharmaceutical Law jobs in the Philippines

Job Summary:
We are looking for a Regulatory Affairs Specialist to ensure that our products comply with all applicable regulations and requirements set by the Food and Drug Administration (FDA Philippines) and other relevant government agencies. The ideal candidate will be responsible for handling product registrations, renewals, license applications, compliance documentation, and regulatory submissions. br>
Key Responsibilities:
Prepare, compile, and submit product registration dossiers to the FDA (Philippines) and other regulatory bodies (e.g., DOH, BFAD, DENR, BOC)
Coordinate with internal departments (e.g., R&D, QA/QC, Marketing) for required documents and technical data
Monitor the status of product approvals, renewals, and license applications
Ensure compliance with all relevant local regulations for pharmaceuticals, food, cosmetics, or medical devices
Maintain and update regulatory files and databases
Provide regulatory advice during product development or marketing planning
Track changes in regulatory legislation and guidelines and communicate these updates to relevant teams
Handle product variations, labeling reviews, and post-market surveillance reports if required
Serve as the company’s point of contact with the FDA and other government agencies < r>
Qualifications:
Bachelor’s Degree in Pharmacy, Chemistry, Biology, Food Technology, or any life science-related field < r>Preferably licensed Pharmacist (for pharmaceutical and drug-related companies)
At least 1–3 years of experience in regulatory affairs or product registration < r>Strong understanding of FDA Philippines regulatory processes and requirements
Excellent attention to detail and organizational skills
Strong communication and documentation skills
Proficient in MS Office (Word, Excel, PowerPoint)
Able to work independently and meet strict deadlines

Preferred but Not Required:
Experience in handling ASEAN Common Technical Dossier (ACTD/ACTR)
Familiarity with GMP, ISO, or HACCP standards (depending on industry)
Experience working with regulatory consultants or third-party laboratories.

Work Schedule:
Monday - Friday | 8am - 5pm

SALARY RANGE: ₱22,000 - 25,000 | Depending on qualifications
WORK SCHEDULE: Monday - Friday | 8:00 AM - 5:00 PM br>WORK LOCATION: Makati | Willing to do Field Work

- At least 1 to 2 years of working experience in the same field / role

Job description
Duties & Responsibilities: br>• Ensures compliance with regulatory requirements and standards in the industry. < r>• Developing and implementing regulatory strategies, collaborating with cross-functional teams, < r>and ensuring that products and processes meet all relevant regulatory guidelines.
• Develop new tools, standards, and approaches to assess the safety, efficacy, quality and < r>performance of all products.
• Develop and execute regulatory strategies and plans to ensure compliance with applicable laws, < r>regulations, and standards.
• Stay updated on changes in regulatory requirements and translate them in actionable steps for < r>the organization.
• Collaborate with cross-functional teams including R&D, Quality Assurance, and Legal to ensure < r>that all regulatory requirements are met throughout the product lifecycle.
• Prepare and submit regulatory submissions, including but not limited to, product registrations, < r>pre-market notifications, and post-market surveillance reports.
• Liaise with regulatory authorities and act as the primary point of contact during inspections, < r>audits, and regulatory agency interactions.
• Conduct risk assessments and develop mitigation strategies to manage regulatory risks. < r>• Review and approve product labelling, promotional materials, and other relevant documentation < r>to ensure compliance with regulatory requirements.
• Provide regulatory guidance and support to internal stakeholders, including product < r>development teams, to ensure that regulatory requirements are incorporated into the
development process.
• Monitor and track regulatory compliance metrics and provide regular reports to senior < r>management.
• Maintain a thorough understanding of international regulations in relevant markets and guide < r>the organization regarding international expansion plans.
Skills & Competencies:
• In-depth knowledge of relevant regulations and standards, such as FDA regulations, ISO < r>standards, and other applicable regional regulations;
• Strong understanding of quality systems and the ability to apply regulatory requirements to < r>quality management processes.
Educational / Work Experiences:
• Graduate of Bachelor in Science degree in Scientific Discipline, Engineering or related field < r>• Master’s Degree is an advantage
Affairs Manager in the food manufacturing industry;
• Proven track record of successfully developing and executing regulatory strategies and obtaining < r>regulatory approvals for products;

• Experience in developing and maintaining regulatory compliance documentation, including < r>technical files, regulatory dossiers, and other relevant documentation;
• Experience in interacting with regulatory authorities and managing regulatory inspections and < r>audits.
Willing to be assigned in Calauan, Laguna
Job Types: Full-time, Permanent

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**
In this role, you will have the opportunity to lead global regulatory efforts for medical devices. Coordinate RF registrations, support product development, and ensure compliance with international RF standards. Act as a key liaison for internal teams and regulatory agencies, managing documentation and assessing impact of design changes on compliance. This will be a remote position in Bogotá.
**Re** **sponsibilities may include the following and other duties may be assigned:**
+ Prepare, obtain and maintain global RF registrations for Medtronic and our third-party radio products.
+ Coordinate and execute global strategies in collaboration with our Operating Units.
+ Support our Operating Units with any RF related queries.
+ Provide RF regulatory support for new products/therapies that include wireless components.
+ Provide impact assessment on RF compliance due to changes to existing products.
+ Work cross-functionally to resolve regulatory queries from regulatory agencies.
+ Manage and maintain technical documentation in line with local RF regulations.
+ Maintain project lists with status and activities for assigned projects.
**Required** **Knowledge** **and** **Experience** **:**
+ Bachelor's Degree in Electric or (bio)medical Engineering. 1-2 years' experience in (Radio) Regulatory function.
+ A basic understanding of electrical engineering and medical device principles.
+ Curiosity and willingness to learn about the international RF regulatory landscape.
+ Strong attention to detail and a proactive, growth-oriented mindset.
+ Excellent communication skills in English and comfort across cultures and time zones.
+ Experience with regulatory submissions of medical devices
+ An electronic engineering background, including basic knowledge of electromagnetism and experience with wireless technologies
+ Desirable skills in automation using Microsoft cloud tools (Power Automate, Power Apps, Power BI, flows)
**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

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**
We're a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Join this newly created team in global Regulatory Affairs and be part of a community that welcomes learners and values growth-we're bringing these devices to markets across the world and looking for those eager to become experts. Step into a role where your ideas matter, your growth is supported, and your work changes lives.
**Responsibilities may include the following and other duties may be assigned.**
+ Prepare, obtain and maintain global RF registrations for Medtronic and our third-party radio products.
+ Coordinate and execute global strategies in collaboration with our Operating Units.
+ Support our Operating Units with any RF related queries.
+ Provide RF regulatory support for new products/therapies that include wireless components.
+ Provide impact assessment on RF compliance due to changes to existing products.
+ Work cross-functionally to resolve regulatory queries from regulatory agencies.
+ Manage and maintain technical documentation in line with local RF regulations.
+ Maintain project lists with status and activities for assigned projects.
**Required Knowledge and Experience:**
+ Bachelor's Degree in Electric or (bio)medical Engineering.
+ 1-2 years' experience in (Radio) Regulatory function.
+ A basic understanding of electrical engineering and medical device principles.
+ Curiosity and willingness to learn about the international RF regulatory landscape.
+ Strong attention to detail and a proactive, growth-oriented mindset.
+ Excellent communication skills in English and comfort across cultures and time zones.
**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

Sr Global Reg Affairs Scientist - PHL/MY - Homebased
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Senior Global Regulatory Scientist to join our diverse and dynamic team. The Senior Global Regulatory Scientist fulfils the role of Global Regulatory Partner (GRP) and is responsible for coordinating all Central Independent Ethics Committee (IEC), Regulatory Agency (RA) and other central authority submissions to ensure contractual timelines are met.
**What you will be doing:**
+ Ensuring regulatory deliverables are performed in accordance with all relevant regulations, guidelines, policies and procedures within contractual timelines and budget with sound scientific/technical principles
+ Developing the overall and global clinical trial submission strategy in accordance with the project requirements in collaboration with stakeholders including proactive identification and mitigation of risks, as applicable
+ Regulatory function team lead overseeing the assigned clinical trial Regulatory project team
+ Point of contact for clients for clinical trial Regulatory deliverables
+ Preparation of clinical trial Regulatory plan in accordance with project specifications
+ Preparation/creation/adaptation/coordination/collation/compliance of global core documents considering strategic, scientific and therapeutic area principles in addition to study requirements
+ Tracking and reporting of submission/approval progress in Clinical Trials Management System (CTMS), eTMF and other applicable systems ensuring accuracy and completeness of data/documents
+ Performing Quality Control review of clinical trial Regulatory deliverables in accordance with applicable process
+ Coordinating submission(s) to regulatory agencies (RAs), central ethics committees (CECs), and all other country-level submissions in collaboration with stakeholders, overseeing the assigned Regulatory project team
+ Coordination of clinical trial label review/approval according to project specifications
+ Managing Regulatory study budget, proactively identifying out of scope activities and supporting budget recognition
+ Supporting the maintenance of accurate, up to date Country and Regulatory Intelligence
+ May work with Regulatory team members to provide Regulatory consulting services
+ May participate in business development activities
+ May mentor junior team members
**Your profile:**
+ Bachelor's degree in a scientific discipline or related field.
+ **Minimum of 3 years of experience in regulatory affairs submissions within the clinical research industry.**
+ Demonstrates complete understanding and application of clinical research regulations, concepts and standards.
+ **Strong understanding of global regulatory requirements and guidelines.**
+ Demonstrates a good understanding of country requirements and how they need to be applied in the clinical trial environment.
+ **Proven history of successful interaction with internal and client teams and a basic understanding of each related function**
+ Excellent English communication and social skills.
+ Ability to work independently and collaboratively in a fast-paced environment.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply

ABOUT UNILEVERWith 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people - we believe that when our people work with purpose, we will create a better business and a better world.At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don't believe in the 'one size fits all' approach and instead we will equip you with the tools you need to shape your own future.ABOUT PERSONAL CARE GREATER ASIA BUSINESS UNIT (BU)Personal Care (PC) business in Greater Asia is a large, profitable, growing market and thus represents a significant growth opportunity in Unilever. We have an ambition to generate over 150M incremental turn-over in the next 3 years and we are accretive to overall PC Business Group (BG). We have a diverse geographical footprint spanning markets like Vietnam, Philippines, Japan, Thailand, Cambodia, and Laos. We see a clear opportunity to grow our core PC brands through market-making (driving penetration & consumption), premiumization (upgradation), and drive competitiveness across channels.As part of the Greater Asia Personal Care Research and Development (PC R&D) , Regulatory Affairs (RA) team will support the Greater Asia PC Business Group (PC BG) ambition by defining and delivering strategically aligned technical advocacy programs, providing regulatory steer and direction to support successful landing of the innovation program and ensuring regulatory compliance in Greater Asia. Since the regulatory framework from almost all Greater Asia countries are linked with the ASEAN regional approach, therefore it will need to collaboration with RA PC Indonesia Lead & RA BW SEA ID Lead to manage our influencing the cosmetic regulation in ASEAN thru ASEAN Cosmetic Association.Who You Are & What You'll DoThe Regulatory Affairs Personal Care Greater Asia Lead will bear the critical responsibility of managing, supporting, and driving all Regulatory Affairs activities across each country seamlessly.
Outlined below are the key responsibilities aligned with the strategic agenda and priorities of the Personal Care R&D:ADVOCACY
+ Work closely with the PC Greater China, Greater Asia & Indonesia RA Lead to establish both short- and long-term regulatory advocacy strategies and priorities. This collaboration aims to ensure smooth business operations and the successful implementation of all PC innovations, including major initiatives and superior claims
+ Identify and implement advocacy opportunities to assist PC R&D in achieving business objectives.
+ Deliver the PC ASEAN advocacy agenda in relevant trade associations e.g., Eurocham, ACA, Vietnam Trade Association and other, collaborate with partners RA B&W SEA & Indonesia Lead, PC Global RA, PC GA R&D, External Affairs, SERS, Communications, and Legal in Greater Asia/Vietnam.
+ Monitors the external environment for regulatory changes and issues impacting the Greater Asia business and cosmetics with support from Local PC RA Leads in each country. This may require knowledge beyond cosmetics, such as packaging, and sustainability, and provides its impact on the PC Greater Asia Business.
+ Raises awareness of regulatory issues and potential impact to PC Greater Asia Business (e.g., legislative developments) to key stakeholders and functions (e.g., RA, R&D, Legal, External Affairs, SC, Comms, Customer Development etc.).
+ Ensure and drive the Unilever Personal Care Business Unit agenda successfully by engaging with local/regional Cosmetic Trade Association through local Personal Care/Beauty & Well-being Regulatory Affairs country leads or regional Personal Care/Beauty & Well-being Regulatory Affairs leads or by her/himself.
+ Represents Unilever with external bodies (Trade Associations, Alliances, regulatory authorities, etc.)
INNOVATION
+ Regulatory input to PC R&D innovation projects
+ Coordinate and provide regulatory assessment input and strategy that could impact PC GA Innovation Projects and PC Global R&D design projects. Collaborate with local PC RA country teams to ensure smooth implementation of all innovation plans within this cluster.
+ Develop strategic plans to support the claims approval process for each country, aiming to achieve superior and bold claims.
COMPLIANCE
+ Monitor the appropriate utilization of RA Digital tools in PC Greater Asia.
+ Support the implementation of Compliance Digital tools in PC RA.
+ Optimize compliance processes in each country to ensure efficiency.
+ Inform the SERS (Safey , Environmental & Regulatory Science) Product Compliance team of new regulatory requirements for Greater Asia.
+ Work closely with local PC RA country teams to monitor and maintaining all the PIF, CSD date based for RA PC Greater Asia and how to handle audits or inspections from local governments or internal auditors smoothly.
+ Connect with the Global Product Compliance team to support PC RA country leads with necessary data.
+ Monitor and maintain all PIF and CSD databases for PC RA Greater Asia, alongside the PC RA Compliance Assistant Manager and the R&D PC Category Team.
TEAM DEVELOPMENT
+ Establish connections within the Global PC RA network to facilitate the communication of issues, issue management, and regulatory updates across R&D and other functions.
+ Develop regulatory talent and foster flexible, agile, and efficient collaborations across business groups and within Greater Asia as appropriate.
+ Ensure the delivery of PC-related regulatory training on relevant scientific areas, legislation, and human/environmental safety to the broader PC RA team, especially within the R&D, Legal, and Supply Chain organizations.
QUALIFICATIONS:
+ Minimum BSc, preferably an M.S. or PhD in Chemistry, Pharmacy or equivalent.
+ Minimum of 6 years experience within an FMCG environment with expertise in Regional Role and ASEAN regulatory requirements that govern Cosmetic Industries.
+ Minimum of 6 years of Advocacy experience in regulatory advocacy within the cosmetics or personal care industry.
+ Demonstrated history of successful engagement with regulatory bodies and industry associations, particularly at both local and regional levels.
+ Demonstrated experience successfully handling regional regulatory work in the cosmetics sector or others, including effective collaboration with a wide range of stakeholders.
+ Strong communication, negotiation, and networking skills to effectively influence policy and regulatory outcomes
+ Proven track record in active collaboration with R&D and non-R&D functions as well as 3rd parties in support of the innovation program.
+ Pro-active self-direction with a high level of initiative and persistence and a hands-on approach to results delivery.
+ Excellent oral and written communication skills Ability to assess regulatory risks and opportunities and the impact it has on the existing and innovation portfolio.
+ Ability to apply argumentation to influence at all levels externally and internally.
+ Clear and logical thinker with the ability to recognize patterns and develop innovative solutions.
We highly encourage applicants to exclude information on age, gender, and school/s in view of Equity, Diversity, and Inclusion. Unilever assesses candidates based on skills, performance, experience and leadership.
Unilever is an organisation committed to equity, inclusion and diversity to drive our business results and create a better future, every day, for our diverse employees, global consumers, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. At Unilever we are interested in every individual bring ing their 'Whole Self' to work and this includes you! Thus if you require any support or access requirements, we encourage you to advise us at the time of your application so that we can support you through your recruitment journey.
Job Category: Research & Development
Job Type: Full time
Industry:

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.
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Emerson's 130+ years of history have been filled with achievements and challenges that have driven innovative thinking and bold transformations, molding us into the company we are today. By joining us as a Legal Governance and Compliance Analyst 1, you will ensure that the business unit's transactions are checked and aligned with the rules and regulation and Emerson's policies on International Trade Compliance and provide support to the business units in managing its trade compliance program.
If this sounds like a perfect fit for you, apply now and join our team in Mandaluyong City, Philippines!
**In This Role, Your Responsibilities Will Be:**
+ To audit the business units' export and import transactions with emphasis on ensuring that the correct export classification codes for its items/parts are used and are in place.
+ Work with the business unit in handling and declaring the appropriate Country of Origin for its products/parts/items.
+ Maintain reports of metrics/KPIs/dashboard to determine performance against business needs.
+ Conduct order and shipment screenings for ISV India
+ Acts as back-up for ISV India ITC gatekeepers
+ Assist the Business Units in screening its export transactions by handling the Tradesphere (TSE) holds for ISV China
+ Assist in developing BU work processes and instructions
**Who You Are:**
You establish clear goals with anticipated outcomes and results. You learn to streamline processes and cut out redundancy and are open to continuing to learn. You research initiatives and try new approaches while staying aligned with your goals.
**For This Role, You Will Need:**
+ Bachelor's Degree in any course
+ At least 1.5 years of experience in trade compliance, product classification, export and import transaction auditing, and Country of Origin Management
+ Good analytical skills and keen attention to details
**Preferred Qualifications that Set You Apart**
+ Experience in product classification and international trade compliance will be an advantage
**Our Culture & Commitment to You**
At Emerson, we prioritize a workplace where every employee is valued, respected, and empowered to grow. We foster an environment that encourages innovation, collaboration, and diverse perspectives-because we know that great ideas come from great teams. Our commitment to ongoing career development and growing an inclusive culture ensures you have the support to thrive. Whether through mentorship, training, or leadership opportunities, we invest in your success so you can make a lasting impact. We believe diverse teams, working together are key to driving growth and delivering business results.
We recognize the importance of employee wellbeing. We prioritize providing competitive benefits plans, a variety of medical insurance plans, Employee Assistance Program, employee resource groups, recognition, and much more. Our culture offers flexible time off plans, including paid parental leave (maternal and paternal), vacation and holiday leave.
#LI-Hybrid
**WHY EMERSON**
**Our Commitment to Our People**
At Emerson, we are motivated by a spirit of collaboration that helps our diverse, multicultural teams across the world drive innovation that makes the world healthier, safer, smarter, and more sustainable. And we want you to join us in our bold aspiration.
We have built an engaged community of inquisitive, dedicated people who thrive knowing they are welcomed, trusted, celebrated, and empowered to solve the world's most complex problems - for our customers, our communities, and the planet. You'll contribute to this vital work while further developing your skills through our award-winning employee development programs. We are a proud corporate citizen in every city where we operate and are committed to our people, our communities, and the world at large. We take this responsibility seriously and strive to make a positive impact through every endeavor.
At Emerson, you'll see firsthand that our people are at the center of everything we do. So, let's go. Let's think differently. Learn, collaborate, and grow. Seek opportunity. Push boundaries. Be empowered to make things better. Speed up to break through. Let's go, together.
**Accessibility Assistance or Accommodation**
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**ABOUT EMERSON**
Emerson is a global leader in automation technology and software. Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability.
With global operations and a comprehensive portfolio of software and technology, we are helping companies implement digital transformation to measurably improve their operations, conserve valuable resources and enhance their safety.
We offer equitable opportunities, celebrate diversity, and embrace challenges with confidence that, together, we can make an impact across a broad spectrum of countries and industries. Whether you're an established professional looking for a career change, an undergraduate student exploring possibilities, or a recent graduate with an advanced degree, you'll find your chance to make a difference with Emerson. Join our team - let's go!
**No calls or agencies please.**
**Requisition ID** : 25023477
Emerson is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.