Total 11 job vacancies by Integrity Partners Pte. Ltd.

Partnering with with a leading global biopharmaceutical company, this is a unique opportunity to gain hands-on experience in a fast-paced, regional Medical Affairs environment.

You will work closely with the APAC Medical team, supporting regional initiatives across multiple markets, gaining real exposure to the healthcare and pharmaceutical industry at a strategic level.

Responsibilities

• Support project management activities: track action items, timelines, and deliverables across regional priorities
• Coordinate meeting logistics including scheduling, agenda preparation, materials, and follow-up actions
• Assist in developing and executing internal medical communications and engagement initiatives (newsletters, townhall preparation, Viva Engage posts)
• Research industry trends, best practices, and competitive landscape to support strategic discussions
• Help maintain and organize team documentation, SharePoint content, and shared resources
• Contribute creative ideas and fresh perspectives to ongoing APAC Medical projects and programs

Requirements

• Available full-time between July 2026 to October 2026; some flexibility can be discussed
• Currently pursuing a degree in Life Sciences, Business, Communications, or related field
• Self-starter with a proactive mindset and eagerness to learn quickly
• Strong organizational skills with attention to detail
• Good communicator—written and verbal—comfortable working in a multicultural, regional team
• Proficient in Microsoft Office (PowerPoint, Word, Excel, Teams, Outlook)
• Ability to manage multiple tasks and adapt in a dynamic environment
• Passion for healthcare, pharmaceuticals, or medical innovation is a plus

If you are curious, proactive, and eager to make an impact—this role is for you.

NEXT STEPS

This is a valuable opportunity for professional development with a global pharmaceutical company as you gain regional exposure and participate in cross-functional collaboration.

If this opportunity excites you, kindly apply with your updated resume in Word format and we will connect shortly for a confidential discussion.

Given the volume of applications, we seek your understanding that only shortlisted candidates will be contacted. Thank you and we truly appreciate your interest.

Ambrose Chan
Registration Number: R1218177
EA License Number: 17C8502

We are seeking a technical, customer-oriented Field Service Engineer to join our team. If you enjoy hands-on troubleshooting and are looking for a role that combines technical mastery with client engagement, we want to hear from you.

Your Role:

• Technical Excellence: Manage installations, testing, commissioning, and repairs of specialized medical equipment.

• Client Advisory: Serve as the go-to technical expert for local customers; provide training on equipment use and maintenance.

• Proactive Support: Conduct preventive maintenance and provide data-driven advice on equipment health and upgrade schedules.

• Growth & Collaboration: Partner with our sales and product teams to support project success and service growth.

Who You Are:

• Qualified: Diploma or higher in Engineering. (Fresh graduates with a strong learning mindset are highly welcome).

• Tech-Savvy: Strong analytical skills with basic IT knowledge (Networking, Windows Server, Active Directory).

• Adaptable: A self-starter who excels at multitasking and works efficiently under pressure.

• Service-Focused: You prioritize customer satisfaction and communicate technical info clearly.

• Flexible: Willing to perform occasional standby duties (after-hours/weekends) as needed.

How to Apply

Interested applicants are invited to submit an updated résumé (in MS Word format) highlighting your relevant experience and project achievements.

Contact Person: Tan Jun Jie

EA Personnel Reg. No.: R1878852

EA License No.: 17C8502

We regret that only shortlisted candidates will be notified.

An excellent opportunity has come up with an international Pharmaceutical MNC and they are currently looking for a Senior Regional Regulatory Affairs Specialist to join the team in Singapore.

The successful incumbent will drive the implementation of global guidelines and work alongside local RA functions to ensure product approvals. You will also exhibit strong interpersonal skills and work closely with cross-functional departments to support the formulation of long-term regulatory strategy.

REQUIREMENTS

• 3 years of regulatory affairs experience in the Pharmaceutical industry
• Experience with regulatory submissions (registrations, post-approval variations)
• Related science degree
• Candidates with adequate Regional experience will be considered for a Senior Specialist position

NEXT STEPS

This is a valuable opportunity for professional development with a global pharmaceutical company as you gain regional exposure and participate in cross-functional collaboration.

If this opportunity excites you, kindly apply with your updated resume in Word format and we will connect shortly for a confidential discussion.

Given the volume of applications, we seek your understanding that only shortlisted candidates will be contacted. Thank you and we truly appreciate your interest.

Ambrose Chan
Registration Number: R1218177
EA License Number: 17C8502

An excellent opportunity has come up with a Healthcare MNC who is a leading player with both their Pharmaceutical and Medical Device offerings. They are currently looking for a Regional Clinical Project Manager to join the team in Singapore.

Responsibilities:

• Implement, execute and complete clinical research project sponsored by Principal according to timelines and budget,
• Be responsible of the compliance to local regulations, GCP regulations, and internal SOPs in clinical projects
• Able to work cross functionally to prepare required study documentations for submission to Ethic Committees and competent authorities which includes oversight, writing and review of documents,
• Develop and manage the overall clinical study budget,
• Select and validate investigator/site, and vendors (i.e CROs),
• Contribute to the negotiation and preparation of contracts and budgets with third parties and sites participating in our studies,
• Responsible of the development of high-quality study documentation (i.e. from study protocol and study plans to final clinical study report) throughout the clinical study,
• Responsible of the management of Contract Research Organizations (CROs) and third-party vendors and ensure adherence to scope of work within timelines and budget,
• Able to work cross-functionally within the clinical team to monitor site performance (such as enrolment and compliance to study protocol), ensure high-quality data collection and review in clinical projects,
• Ensure that all relevant documents are properly and timely archived in the TMF during the study,
• Participate in the internal process of improvements.

Requirements:

• Bachelor’s degree, preferably in Medical Science
• Excellent knowledge of NIS/IITs and Sponsored Trials
• Possess minimum 5 years’ of experience in Clinical Trial Management for dermatology across APAC/China/Japan
• Excellent communication skills, particularly in stakeholder interactions.
• Ability to work in fast paced, dynamic and high pressure situations
• Frequency of travel: 30% across APAC

For more information, please apply with a word format CV.

Ambrose Chan

Registration Number: R1218177

EA License Number: 17C8502

Our client is a leading global medical device MNC, and we are seeking a results-oriented sales professional who is driven, motivated, and ready to drive sales success in this role.

Job Responsibilities:

• Manage sales call and sales leads with hospitals/specialist centers.
• Build relationships and maintain strong network with existing accounts to support customers' requirements and future needs.
• Work closely with marketing team to understand the benefits and use of medical devices as well as supporting workshops and launch of new products, roadshow and other sales leads.
• Provide product technical support in Operating Theatre cases.
• Communicate between sales, marketingand support teams to improve customer experience.
• Collect, analyze and present field sales date to assist with strategy planning and implementation and gain clear understanding to grow our market share.
• Update sales report on daily activities/events to the management.

 Requirements:

• Degree or Diploma in Bioengineering/equivalent
• At least 2 years of relevant experience in medical device/instrument sales will be an advantage.
• Positive attitude with a focus on results
• Committed to meeting deadlines and delivering on time
  

How to Apply:

Interested applicants may apply by submitting your updated CV (inMS Word format). We regret that only shortlisted candidates will be notified.

Consultant: Henry Zheng

Registration Number: R1106964 

EA License Number: 17C8502

An excellent opportunity has come up with an international Pharmaceutical MNC and they are currently looking for a Senior Regional Regulatory Affairs Specialist to join the team in Singapore.

The successful incumbent will drive the implementation of global guidelines and work alongside local RA functions to ensure product approvals. You will also exhibit strong interpersonal skills and work closely with cross-functional departments to support the formulation of long-term regulatory strategy.

REQUIREMENTS

• 3 years of regulatory affairs experience in the Pharmaceutical industry
• Experience with regulatory submissions (registrations, post-approval variations)
• Related science degree
• Candidates with adequate Regional experience will be considered for a Senior Specialist position

NEXT STEPS

This is a valuable opportunity for professional development with a global pharmaceutical company as you gain regional exposure and participate in cross-functional collaboration.

If this opportunity excites you, kindly apply with your updated resume in Word format and we will connect shortly for a confidential discussion.

Given the volume of applications, we seek your understanding that only shortlisted candidates will be contacted. Thank you and we truly appreciate your interest.

Ambrose Chan
Registration Number: R1218177
EA License Number: 17C8502

Partnering with a Medical Device MNC with an established branding, our client is seeking a Senior Regulatory Affairs Executive as part of their expanding setup in Singapore.

Reporting to the Senior Regulatory Affairs Manager, we are looking for someone with good knowledge of regulatory framework in Singapore.

In this position, you will prepare technical dossiers for submission to Europe (CE Mark) and US FDA (510K) and also work closely with regional affiliates to help them obtain product approval.

You should have at least 3 years’ of regulatory experience in medical devices and a related science degree.

NEXT STEPS
If this opportunity excites you, kindly apply with your updated resume in Word format and we will connect shortly for a confidential discussion.

Given the volume of applications, we seek your understanding that only shortlisted candidates will be contacted. Thank you and we truly appreciate your interest.

Ambrose Chan
Registration Number: R1218177
EA License Number: 17C8502

The Role: Lead the setup and validation of critical utility systems for a major Greenfield biopharma plant in Singapore.

Key Responsibilities:

• Startup: Oversee installation and commissioning of pharma-grade utilities.

• Maintenance: Build and manage PM programs using SAP/Maximo.

• Ops Support: Rapid troubleshooting of mechanical failures during GMP runs.

• Compliance: Ensure all systems are 100% audit-ready.

Must-Haves:

• Degree in Mechanical/Electrical/Chemical Engineering.

• Expertise in HVAC and WFI (Water for Injection) systems.

• Solid background in GMP environments.

How to Apply:

Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:

Consultant: Tan Jun Jie

EA personnel reg. no.R1878852

EA License No. 17C8502

The Role: Serve as the technical bridge between R&D and full-scale commercial manufacturing for a leading Biopharma site.

Key Responsibilities:

• Scale-Up: Lead the seamless transfer of process technology to large-scale production.

• Shop Floor: Provide real-time technical troubleshooting during live GMP batches.

• Optimization: Analyze production data to identify trends and improve yield.

• Monitoring: Spearhead engineering runs and process monitoring dashboards.

Must-Haves:

• Degree in Biochemical/Chemical Engineering or Biotechnology.

• Strong knowledge of Upstream (Cell Culture) or Downstream (Purification).

• Direct experience with Tech Transfer in a GMP facility.

How to Apply:

Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:

Consultant: Tan Jun Jie

EA personnel reg. no.R1878852

EA License No. 17C8502

Overview

Our Client is looking for a highly skilled and experienced Senior Front-End Web Developer to join our team in Singapore. We are committed to excellence, creativity, and cutting-edge technology, and we need a talented developer to help us deliver exceptional user experiences as we expand our digital presence.

In this crucial position, you will support our new R&D team and drive product evolution development initiatives.

Core Responsibilities

• SPA Development: Engineer and maintain high-performance SPAs using React or Angular with TypeScript and Node.js.

• Performance Tuning: Optimize application speed and asset management via Webpack.

• Data Connectivity: Integrate systems with RESTful APIs, GraphQL, and third-party services.

• Secure Access: Implement robust OAuth, JWT, and OpenID authentication protocols.

• Automated Testing: Ensure code reliability using Jest or Jasmine for unit and integration tests.

• DevOps & Deployment: Manage Docker containerization and CI/CD automation pipelines.

• UI/UX Integration: Convert Figma designs into functional HTML assets in collaboration with design teams.

• Technical Synergy: Work with architects and cross-functional teams to deliver enterprise-grade code.

Requirements

• Education: Degree in Computer Science, Engineering, or a related field.

• Experience: 3–4+ years in front-end development, specifically with complex enterprise solutions.

• Methodology: Proficient in Agile/Scrum environments and iterative workflows.

• Leadership: Capable of guiding teams and coordinating across functions to hit goals.

• Domain Knowledge (Bonus): Background in FinTech or HR tech systems is a plus.

• Soft Skills: Strong problem-solving, communication, and the ability to thrive in fast-paced settings.

How to Apply

Interested applicants are invited to submit an updated résumé (in MS Word format) highlighting your relevant experience and project achievements.

Contact Person: Tan Jun Jie

EA Personnel Reg. No.: R1878852

EA License No.: 17C8502

We regret that only shortlisted candidates will be notified.

Partnering with a Medical Device MNC with an established branding, our client is seeking a Senior Regulatory Affairs Executive as part of their expanding setup in Singapore.

Reporting to the Senior Regulatory Affairs Manager, we are looking for someone with good knowledge of regulatory framework in Singapore.

In this position, you will prepare technical dossiers for submission to Europe (CE Mark) and US FDA (510K) and also work closely with regional affiliates to help them obtain product approval.

You should have at least 3 years’ of regulatory experience in medical devices and a related science degree.

NEXT STEPS
If this opportunity excites you, kindly apply with your updated resume in Word format and we will connect shortly for a confidential discussion.

Given the volume of applications, we seek your understanding that only shortlisted candidates will be contacted. Thank you and we truly appreciate your interest.

Ambrose Chan
Registration Number: R1218177
EA License Number: 17C8502