Total 22 qa manager job vacancies in Quality Assurance / Control category in The United States of America

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you!

The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement.

This is a contract position offered initially on a 12 month contract basis working 37.5 hours a week Mon-Fri.

Responsibilities:

• Perform QC Review of documents.
• Verify data in assigned documents against source documentation, including checking text against database outputs.
• Perform editorial and technical review for grammatical and stylistic consistency in line with the Style Guide and document templates. This includes reviewing format, internal linking, and external cross-referencing.
• Document QC findings so that appropriate actions can be taken by authors. Where needed, meet with the author to discuss findings and strategize the next steps (in case the error lies within the source document), including support with the development of preferred text.
• Document QC metrics for quality tracking.
• Review vendor authoring and QC as part of oversight activities.
• Support the creation of training material for new staff members and vendors on quality requirements.
• Support the preparation of aggregate report quality trends for discussion at regular team meetings.
• Assist with the development and maintenance of training materials and Job Aids.
• Assist with maintenance of SSA templates.
• Assist with SSA process improvement initiatives for quality documentation and technical tools/systems, including developing new templates.
• Represent the department, where appropriate, in cross-functional improvement initiatives.
• Perform general administrative tasks such as maintaining spreadsheets and communicating summaries and results with the relevant stakeholders.
• Provide support to other functions within SSA, which may include activities outside of QC review (e.g., vendor management, aggregate report processes, SharePoint maintenance, literature activities).

Experience and skills:

• Bachelor's Degree in biologic, natural science, or health care discipline.
• Advanced degree (PhD, MPH, NP, PharmD, etc.) preferred.
• Previous writing and editing experience, preferably in the pharmaceutical or biotech industry.
• Comfortable with medical concepts and terminology; familiar with the American Medical Association (AMA) Manual of Style.
• Familiar with pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and postmarketing safety regulations. Includes familiarity with case processing, expedited reporting rules, and safety database concepts.
• Ability to understand, interpret, analyse, and clearly present scientific and medical data in verbal and written format.
• Ability to interact collaboratively and effectively in a team environment.
• Strong organisational skills, including the ability to prioritise independently.
• Proficient and comfortable using Microsoft Office (in particular, Word, Excel, and PowerPoint) and SharePoint platforms.
• Familiar with Documentum-based systems.
• Knowledge of common safety database systems.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

about company

I am currently working with a well known biotechnology research company. Office located in Woodlands - but there's shuttle bus provided from multiple MRT stations.

Hybrid working arrangement now. Working hours 8am to 5pm. Can end work at 5pm and have more personal time.

about job

● Develop end to end automated integration, verification and continuous integration system

● Develop, maintain and enhance automated test framework, tools and unit tests

● Work with software engineers and bioinformatics scientists to understand analysis algorithms & develop automated test solution(s)

● Partner with software verification engineers to test applications manually as needed

● Prepare necessary test artifacts required for formal software / product release

skills and requirements

● Bachelor of Science degree in in computer science or related field

● Min 5 years of experience

● Software test development experience with programming or scripting language (Python preferred)

● Experience in architecting end-to-end automated test suite for API, desktop, web apps and experience with test frameworks such as pytest, Playwright, or similar

● Experience writing verification plans, test cases, defects reports, executing & managing test cases using test cases management system and writing verification reports

● Experience working with databases such as MySQL or PostgreSQL, cloud computing such as Amazon Web Services and Docker/Kubernetes

● Experience with CI/CD, Continuous Testing

To apply online please use the 'apply' function, alternatively you may contact Stella at 96554170 (EA: 94C3609 /R1875382)

To apply, It will be great if you could share your CV to hoonteck.tan@randstad.com.sg. Alternatively, you can apply at https://lnkd.in/gMAzSD7b

• Interaction with global IT HQ
• Large scale project

About the company

Our client is a market leader within their industry. With massive expansion plan in Asia, they are recruiting a new QA Software Test Specialist APAC (Java, Selenium) to join their team.

About the job

Your role includes:

• Providing and implementing QA test plan for the company. Being the key point of contact for all QA aspects of releases, providing QA services and coordinating resource
• Creating test scripts for automated execution based on user stories and test cases. This includes defining and evolution of test plans, cases, matrix and execution results analysis.
• Managing the off-shore resources, assigning of work and coordinating resources for testing/QA projects
• Creating the Performance testing plan and strategy for projects. This includes establishing priorities and integration logical diagrams, conducts tests in factory and on site, supports acceptance as well as commissioning, analyses results and communicates them to development teams.
• Ensuring quality and the design of software testing and improvements to maintain the business reliability. This includes ensuring the validity of all testing artefacts required during the Build and Test Phases of the SDLC project delivery methodology
• Driving lessons learned activities for prevention/corrective actions in the future

Skills and experience required

As a successful applicant, you will have at least 5 year of experience in Test/ QA. Exposure to At - test strategy/plan will be of added advantage.

Candidates from end user background with cloud experience will be of added advantage.

Whats on offer
This is an excellent opportunity to join a MNC with exposure to high value projects.

To apply, It will be great if you could share your CV to hoonteck.tan@randstad.com.sg. Alternatively, you can apply at https://lnkd.in/gMAzSD7b (EA: 94C3609/ R1219669)

about the company

Our client is a leading materials testing laboratories and solutions provider for a wide range of fields including construction, life sciences, environmental, energy, transportation etc. They’re now on a look out for a Quality Engineer/Manager to join their dynamic team.

about the job

• Implement, maintain and improve the quality management system (QMS)
• Drive quality improvements and proactive participation in continuous improvement and process improvement projects
• Represent our Singapore and Malaysia business units during assessments by accreditation bodies and audits by clients and controlled document holding
• Interact with clients & Accreditation Bodies and be responsible for advising operational colleagues of the importance of quality, accuracy and integrity in the provision of the testing, calibration inspection and certification services we provide.
• Ensure buy-in to the effective implementation of our quality policies and procedure
• Manage scheduled internal audits across management system and technical disciplines
• Monitor laboratory test equipment for calibration currency and advise management of upcoming schedules,ensuring corrective and preventive actions identified within specific laboratories are implemented and verified in a timely manner.
• Manage external and internal proficiency testing programs and prepare compliance and improvement metrics as required.
• Write and review quality documentation and effective and efficient management of personal work schedules and timely generation of quality reports.

job requirement

• Diploma/Degree of Science or Engineering qualification.
• Minimum 2 years of managing quality management systems within a multi-discipline testing, inspection and certification environment
• Candidates with more experience (min 4 years) can be considered for the Quality Manager position.
• Demonstrable experience auditing against ISO/IEC 17025, ISO/IEC 17020 and ISO/IEC 17065.
• Sound knowledge of equipment calibration and analyzing proficiency test data.

If you are interested in the position, kindly apply directly or send your CVs to yiling.tan@randstad.com.sg.

We regret that only shortlisted candidates will be contacted

EA: 94C3609 / Reg: R21103172

about the company

Our client is a biotech company reputable for their immunotherapies with the aim to meet the needs in cancer treatment. With a world-leading combination of technology transfer and their in-house R&D, they are well positioned with global talents in the industry. They’re now looking for a dedicated QC Manager to join their team during this exciting time.

about the job

• Perform quality control tests for clinical materials (cell therapy products) according to GMP standards.
• Work with the Cell Manufacturing & Quality Assurance Team.
• Ensuring GMP compliance is maintained at all times.
• Be accountable for the highest level of execution of regulatory strategies, and standards of quality compliance.

job requirement

• Degree in cell biology/biomedical sciences or in a similar medical technology related field.
• Possess experience in quality control tests of biologics or immune cell products
• Experience in regulatory filing with FDA/HSA is desired.
• Familiar with regular testing methods (i.e. sterility/mycoplasma/endotoxin detection, flow cytometry analysis; Cytokine measurement assays; qPCR assays etc.)

If you are interested in the position, kindly apply directly or send your CVs to yiling.tan@randstad.com.sg.

We regret that only shortlisted candidates will be contacted.

EA: 94C3609 / Reg: R21103172

about the company

Our client is a leading materials testing laboratories and solutions provider for a wide range of fields including construction, life sciences, environmental, energy, transportation etc. They’re now on a look out for a Quality Engineer/Manager to join their dynamic team.

about the job

• Implement, maintain and improve the quality management system (QMS)
• Drive quality improvements and proactive participation in continuous improvement and process improvement projects
• Represent our Singapore and Malaysia business units during assessments by accreditation bodies and audits by clients and controlled document holding
• Interact with clients & Accreditation Bodies and be responsible for advising operational colleagues of the importance of quality, accuracy and integrity in the provision of the testing, calibration inspection and certification services we provide.
• Ensure buy-in to the effective implementation of our quality policies and procedure
• Manage scheduled internal audits across management system and technical disciplines
• Monitor laboratory test equipment for calibration currency and advise management of upcoming schedules,ensuring corrective and preventive actions identified within specific laboratories are implemented and verified in a timely manner.
• Manage external and internal proficiency testing programs and prepare compliance and improvement metrics as required.
• Write and review quality documentation and effective and efficient management of personal work schedules and timely generation of quality reports.

job requirement

• Diploma/Degree of Science or Engineering qualification.
• Minimum 2 years of managing quality management systems within a multi-discipline testing, inspection and certification environment
• Candidates with more experience (min 4 years) can be considered for the Quality Manager position.
• Demonstrable experience auditing against ISO/IEC 17025, ISO/IEC 17020 and ISO/IEC 17065.
• Sound knowledge of equipment calibration and analyzing proficiency test data.

If you are interested in the position, kindly apply directly or send your CVs to yiling.tan@randstad.com.sg.

We regret that only shortlisted candidates will be contacted

EA: 94C3609 / Reg: R21103172

about company

I am currently working with a well known biotechnology research company. Office located in Woodlands - but there's shuttle bus provided from multiple MRT stations.

Hybrid working arrangement now. Working hours 8am to 5pm. Can end work at 5pm and have more personal time.

about job

• Work as part of Agile scrum teams to design, implement, and test the instrument control software that powers our industry-leading DNA sequencing and genotyping devices
• Develop end to end automated integration, verification and continuous integration system
• Develop, maintain and enhance automated test framework, tools and unit tests
• Collaborate with DevOps to design and manage an automated, computational infrastructure supporting experimentation and research
• Design and code test scripts, deploying to build pipeline, monitoring results

skills and requirements

• Bachelor of Science degree in in computer science or related field
• Min 5 years experience in testing and supporting software for mechanical instrumentation
• Software test development experience with programming and scripting languages (C#, TypeScript, shell script preferred)
• Experience in architecting end-to-end automated test suite for API, desktop, web apps and experience with test frameworks such as pytest, Playwright, or similar
• Experience in writing verification plans, test cases, defects reports, executing & managing test cases using test cases management system and writing verification reports
• Experience with CI/CD, Continuous Testing, and related tools such as TeamCity, Jenkins, GitHub Actions
• Experience in developing instrument software / hardware integration is a plus
• Experience in biotech and bioinformatics is a plus
• Experience in Linux Operating System is a plus

To apply online please use the 'apply' function, alternatively you may contact Stella at 96554170 (EA: 94C3609 /R1875382)

about the company

Our client is a biotech company reputable for their immunotherapies with the aim to meet the needs in cancer treatment. With a world-leading combination of technology transfer and their in-house R&D, they are well positioned with global talents in the industry. They’re now looking for a dedicated QC Manager to join their team during this exciting time.

about the job

• Perform quality control tests for clinical materials (cell therapy products) according to GMP standards.
• Work with the Cell Manufacturing & Quality Assurance Team.
• Ensuring GMP compliance is maintained at all times.
• Be accountable for the highest level of execution of regulatory strategies, and standards of quality compliance.

job requirement

• Degree in cell biology/biomedical sciences or in a similar medical technology related field.
• Possess experience in quality control tests of biologics or immune cell products
• Experience in regulatory filing with FDA/HSA is desired.
• Familiar with regular testing methods (i.e. sterility/mycoplasma/endotoxin detection, flow cytometry analysis; Cytokine measurement assays; qPCR assays etc.)

If you are interested in the position, kindly apply directly or send your CVs to yiling.tan@randstad.com.sg.

We regret that only shortlisted candidates will be contacted.

EA: 94C3609 / Reg: R21103172

Are you an experienced QA Engineer with a background in Post Market Surveillance? Are you familiar with cGMP and/or ISO Quality System requirements?

We are recruiting for a QA Engineer to ensure compliance to site and divisional policies and procedures. The successful candidate will also be supporting the continuous improvement and effective maintenance of the QMS, supporting the use of appropriate risk management tools to prioritise activities and level of effort required, support the building and maintenance of successful cross functional relationships with departments such as R&D, Technical, Engineering, Operations and Regulatory Affairs in order to achieve all project goals.

The successful candidate will be joining a global Diabetes Care business based in Witney, working 37.5 hours per week on an initial 6 month contract basis.

Responsibilities:

• Support the review and approval of protocols and reports for Software, Facilities Utilities Equipment, Test Method, and Process validations
• Monitoring and maintenance of the process FMEA and risk analysis records
• Provide input into sampling plans and validation statistical methods
• Maintenance of the site validation plans, listings and periodic review process
• Validation input to post market surveillance activities
• Support the maintenance of Risk Management plans and associated records e.g. design risk analysis and design FMEA
• Support the design input to post market surveillance activities and product performance monitoring
• Monitoring and documentation of Post Market Surveillance activities including clinical performance monitoring
• Support the change control process including, assessment of impact and review, approval and authoring of documentation
• Support the CAPA process by identifying and raising Quality / Compliance issues, reviewing Exception Reports and confirming Corrections and Corrective Actions
• Support Operations to make Quality / Compliance decisions on product during processing, manufacturing, testing, monitoring and packaging
• Project manage ER's / Post Investigations / Deviations within agreed timelines
• Coordinate cross functional team activities to ensure ER investigations establish root cause and identify appropriate Corrective Actions
• Work with end users of the POMS system to triage issues and support driving to resolution
• Post Market Surveillance
• Responsible for supporting the gathering data for product surveillance
• Support the data requests required monthly, quarterly, semi-annual, or ad-hoc reports for management review, postmarket surveillance or other activities as required
• Support postmarket surveillance metrics

Experience & Qualifications:

• Scientific background
• Exposure to in Post Market Surveillance
• Ability to work with a variety of databases
• Ability to handle data / spreadsheets / interpret data
• Strong time management skills
• Strong planning capabilities
• Ability to adapt to changes throughout the week / re-plan

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

about the company

My client is a specialised manufacturer serving the machinery/equipment market. They are a Chinese MNC and with their innovating technology, this is a great brand to join at an exicting time in their development. The role needs the candidate to be based permanently in Hanoi, Vietnam

about the job

• Leader of the Quality Department
• Work with a cross-functional team to manage quality issues in New Production Introductions (NPI) program, resolving issues in material or process to successfully reach mass production
• Work with Purchasing and Engineering Team to develop local sourcing and manage supplier quality issues
• Establish control plans based on customer requirements and PFMEA for incoming, in process, outgoing and reliability inspection
• Drive the implementation of process control in critical process that will impact product quality
• Initiate activities and programs for continuous improvement on product quality and manufacturing processes
• Manage field returns and complaints

skills & experience required

• Master / Degree in Electrical / Mechanical / Manufacturing Engineering or equivalent
• Minimum 10 years of experience in contract manufacturing / services (EMS) environment
• Prior NPI manufacturing experience will be a plus
• Extensive Experience in supplier & product quality management
• Six sigma certified / lean manufacturing / continuous improvement techniques a plus
• Have good understanding of PPAP, and quality tools like MSA, SPC & FMEA
• Will be based in Hanoi, Vietnam permanently

If you are interested in the position , kindly send your CVs in to yitwei.kwan(@)randstad.com.sg
Please include your availability, expected salary and reason for leaving current job.
We regret that only shortlisted candidates will be contacted
EA: 94C3609 / Reg: R1325913

about the company

Our client is a leading total solutions provider for residential, commercial and industrial standby/emergency power, distributed power and recreational power etc. They’re looking for a Quality Manager to join their dynamic team.

about the job

• Implements effective quality system processes in line with ISO9001.
• Develops and leads quality assurance function/team and QMS quality planning process
• Ensures operational process operating and meeting process/ product requirement
• Closely monitors the performance of key quality indicators (Quality objectives) and initiates, deploys and implements plans or measures to meet the goal set.
• Leads team to review daily process issues and drive respective departments for process improvement.
• Analyzes process weakness and/or quality performance data and works with the respective department on a quality improvement plan.
• Ensures all documents are updated regularly.
• Participates in quality improvement programs.
• Ensures that the company is readily prepared for customer audits, internal audits and/or external audits

job requirement

• Diploma/Degree in Quality/Manufacturing/Mechanical/Electrical Engineering
• Minimum 5 years’ relevant experience in a similar position
• Good knowledge in Autocad, SAP, ISO auditing and statistical tools, MS office platforms
• Experience working in an ISO 9001:2000 Quality System.
• Proficient in the use of mechanical inspection equipment including calipers, micrometer, torque tester and other mechanical equipment.
• Willing to work in the West

If you are interested in the position, kindly send your CVs to yiling.tan@randstad.com.sg.

Please include your availability, expected salary and reason for leaving your current job.

We regret that only shortlisted candidates will be contacted.

EA: 94C3609 / Reg: R21103172

Are you a Quality Manager, looking to work on an exciting project in the Hampshire area? Are you looking to work with a well known contractor, who hold an excellent reputation in the area?

If so, read on...

We are looking for a Permanent Quality Manager in the Portsmouth area!

Salary: £50,000 - £60,000

Employment Type: Permanent

Start Date: ASAP

The Project:

This client has a diverse portfolio of civil engineering schemes ranging from access road improvements, public realm works, highways schemes, water treatment works, marine works and specialist framework projects.

The specific projects that you would be working on initially would be water and marines. Therefore, experience in these areas would be advantageous.

The Role:

This is the perfect opportunity working with a well known civils contractor, who hold an excellent reputation Nationwide.

This role will be site based, with the occasional need to spend time in the Head Office.

You will be responsible for:

• Ensuring Inspection Test Plans (ITPs) are producied accurately and in a timely manner
• Reviewing ITPs
• Managing materials testing for subcontractors
• Producing all quality documents and issuing to the client
• Managing all test results and ensuring all are issued to the client or relevant party
• Developing quality forms and checklists
• Ensuring works are approved in a timely manner, to ensure that the construction stages remain on programme
• Liaising with project management and site team to improve the quality of work produced
• Daily liaison with the client, designers and all relevant third parties
• Developing and implementing quality control processes and procedures
• Monitoring the project quality and performance

Requirements:

• Ideally experience in civil engineering projects and specifically water projects
• Excellent understanding of quality within the Design Process
• Excellent with record keeping and data management
• Good communicator
• Experience working on a large scale, complex civil engineering project
• An understanding of working closely alongside other contractors
• Full driving license
• CSCS Card
• Degree or HNC in Construction Management, Engineering or a relatable industry
• Microsoft Word, Excel, Outlook and Sharepoint

if this role sounds of interest to you or if ypou know someone who may be interested, please contact Louise Pridmore @ Randstad on 01622 357230 (option 2) or apply online.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

Are you a dedicated and experienced Quality Manager looking for your next career opportunity? If so, we have an exciting position waiting for you!

Position: Group Quality Manager About the client:
They're a leading civil engineering and construction company, with a rich history of delivering high-quality projects across the UK and beyond. We are committed to excellence, innovation, and safety, and we are looking for a Group Quality Manager who shares our passion for delivering top-notch results.

Role Overview:
As the Group Quality Manager, you will be responsible for ensuring that our projects meet and exceed quality standards. You will work closely with project teams, promoting a culture of continuous improvement and maintaining our commitment to safety and sustainability.

Key Responsibilities:

Develop and implement quality control processes and procedures.
Monitor project quality and performance.
Ensure compliance with industry standards and regulations.
Collaborate with cross-functional teams to drive quality improvement.
Lead quality audits and provide training as needed.
Contribute to our commitment to safety and environmental sustainability.

Requirements:

Proven experience in a quality management role, preferably within the construction or civil engineering sector.
Strong knowledge of quality control principles and standards.
Excellent problem-solving and analytical skills.
Exceptional communication and leadership abilities.
A commitment to safety and sustainability.

Benefits:

Competitive salary and benefits package.
Opportunities for career growth and development.
A collaborative and dynamic work environment.
The chance to work on exciting and challenging projects.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

about the company

Our client is a tech consultancy company that specializes in developing web and mobile applications in the gaming industry.

about the job

• Work closely with backend software engineers to tune code and databases
• Unit Test execution and development using Junit framework and IntelliJ Integrated Development Environment
• Liaise with internal & external teams to identify system requirements and constantly improve test scope accuracy
• Log and track defect using Jira and follow-up to closure
• Mentor peers by cultivating curiosity and technical understanding
• Work closely with other QA team to deliver high quality releases
• Conduct code reviews to ensure unit testing code quality
• Constantly looks for improvements in software development and testing processes
• Perform other duties as assigned

skills and experience required

• Bachelor’s Degree in Computer Science or equivalent
• Exposure or knowledge in whitebox testing
• Exposure or knowledge in Java SpringBoot framework
• Exposure or knowledge in unit testing such as JUnit framework
• Hands-on experience working with Oracle database
• Hands-on experience with IDE (IntelliJ), distributed source control (Git) & CI tool (Jenkins)
• Experience with RESTful(Representational State Transfer) API, 3-tier architecture
• Solid knowledge of software QA methodologies, tools and processes.
• Thorough Understanding of API/integration testing
• Experience in working with agile life cycle and/or tracking and process management tools (JIRA)
• Proven ability to identify and resolve the root cause of system defects
• Proven QA experience in testing highly distributed and complex systems, with an ability to think tactically as well as strategically
• Excellent teamwork and collaboration skills
• Capable to work under pressure
• Desire to share knowledge for the improvement of others
• Experience with performance test is a plus
• Understanding of SOLID principle is a plus
• Experience with Katalon or similar software testing framework is a plus
• Experience in designing and building test tools and systems is a plus
• Strong analytical skills, creative, and detail oriented
• Self-motivated and able to work independently
• Proficient in Mandarin to liaise with clients in China

To apply online please use the 'apply' function, alternatively you may contact Kaixinn at kaixinn.chew@randstad.com.sg

(EA: 94C3609/ R2196712)

about the company

Our client is a licensed Fund Manager with a dynamic work environment and a fast-growing international footprint. They are looking to hire for their compliance team to assist the business in operating in adherence to local regulations.

about the job

Your role responsibilities include:

• Advising business as well as updating company policies as necessary with regards to relevant MAS notices and relevant regulations under the Securities and Futures Act (SFA) as well as Capital Market Licensee conditions
• Manage the Anti-Money Laundering and Counter Financing of Terrorist (AML/CFT) programme, and assist with client onboarding, periodic reviews, etc.
• Continually enhancing the compliance framework and assisting with regulatory and compliance matters with respect to local as well as global operations
• Facilitating in internal and external audits
• Work closely with external vendors such as the fund administrator, corporate agents, external counsel etc.
• Conducting training on compliance matters for all staff

skills and experience required

• Degree in Accountancy, Banking, Business or Law, or relevant professional qualification in financial services or audit
• 5-8 years of relevant experience in Compliance positions within the Asset Management/ Investment Management sector
• Excellent communication and interpersonal skills

To apply online please use the 'apply' function, alternatively you may contact <Daniella Koh> at <daniella.koh(@)randstad.com.sg>.
(EA: 94C3609/ <R1655148>)