Total 14 job vacancies by Integrity Partners Pte. Ltd.

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

Our client, an innovative pharmaceutical company, is seeking a medical sales professional to drive sales and play a key role in supporting marketing activities for the assigned product range.

Key Responsibilities:

• Promoting key products by detailing the features, advantages, benefits and unique selling points of the assigned portfolio
• Deliver sales targets and reporting on sales and business development, including updates on competitor activity
• Support in product launches and marketing activities (online and offline)
• Execute effective call reports and meet business KPIs
• Actively build and maintain current and potential customer relationships
• Provide feedback to managers regarding customers, markets and product performance and issues.

Requirements:

• Degree in pharmacy/life sciences or equivalent.
• At least 3 years of relevant experience in pharmaceutical sales targeting hospitals and specialists and a proven track record in achieving sales target.
• Independent, resourceful, self-driven, result-oriented.
• Valid Class 3/3A driving license and own transport.

Interested applicants may apply directly. We regret that only shortlisted candidates will be notified.

Consultant: Henry Zheng

EA Registration No: R1106964

EA Licence No: 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 an MNC leader in Consumer Health, we are seeking a Regional Events Manager (APAC) to join their marketing team. This role will involve overseeing the planning, development, and production of customer and media-facing events.

Responsibilities:

• Overseeing event planning, management, and successful delivery, including conferences, virtual and live events, awards ceremony, road shows, promotions, exhibitions, and summits in SEA and/or Asia Pacific

• Responsible for events related theme and related event’s communication materials .

• Helm a customer-facing awards ceremony while reviewing its award criteria and conditions yearly to ensure that it ties in with the company commercial objectives

• Research for available venues and recommends event sites; investigates, selects, negotiates and coordinates services with vendors, including F&B catering needs

• Proven ability to think strategically, creatively and manage projects from initiation to completion, including agency management, planning, budgeting, timeline management, supplier coordination, resource allocation, and digital integration.

• Playing a key role in preparing high-quality proposals and presentations that showcase innovative ideas with excellent oral and written communication skills to present to leadership team with a cohesive, influential story to each event

• Championing the development and implementation of new approaches/technologies for successful events.

• Overseeing event setup and production, ensuring efficient supplier and contractor management.

• Prepares budgets and forecasts and compiles summaries of total event costs, cost-per-contact, audience profiles and attendees' comments.

• Compiling comprehensive post-event reports to evaluate success and identify areas for improvement.

Requirements:

• Bachelor’s degree, preferably in Marketing, Events Management

• Minimum 6 years of working experience in event management.

• Proven track record of successfully delivering in-person, virtual, and hybrid events.

• Extensive experience working on diverse projects, including exhibitions, seminars, product launches, promotions, live events, and conferences, showcasing versatility and adaptability.

• Excellent communication skills, particularly in stakeholder interactions.

• Strong experience in proposal preparation and delivering impactful presentations.

• Willingness to travel overseas for work, if required

• Demonstrated problem solving and decision-making skills.

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

Our client, an innovative pharmaceutical company, is seeking a medical sales professional to drive sales and play a key role in supporting marketing activities for the assigned product range.

Key Responsibilities:

• Promoting key products by detailing the features, advantages, benefits and unique selling points of the assigned portfolio
• Deliver sales targets and reporting on sales and business development, including updates on competitor activity
• Support in product launches and marketing activities (online and offline)
• Execute effective call reports and meet business KPIs
• Actively build and maintain current and potential customer relationships
• Provide feedback to managers regarding customers, markets and product performance and issues.

Requirements:

• Degree in pharmacy/life sciences or equivalent.
• At least 3 years of relevant experience in pharmaceutical sales targeting hospitals and specialists and a proven track record in achieving sales target.
• Independent, resourceful, self-driven, result-oriented.
• Valid Class 3/3A driving license and own transport.

Interested applicants may apply directly. We regret that only shortlisted candidates will be notified.

Consultant: Henry Zheng

EA Registration No: R1106964

EA Licence No: 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