Total 815 financial analyst job vacancies in Quality Assurance / Control category in Malaysia

Quality Control Analyst & Senior QC Analyst urgently required for our client in the Sandwich area.

These are exciting full-time permanent positions, 37.5 hours per week, 8am to 5pm, with an hour's lunch. Competitive salary of £27,000 per annum (£30,000 per annum for the senior role), plus a host of benefits, to include:

• 31 days annual leave, inclusive of Bank Holidays - increasing with length of service
• Auto enrolled pension scheme
• Healthcare, Death in Service, Private Medical insurance including dependants
• Annual bonus scheme
• Free parking
• Great working environment

* You must be committed to your role and have HPLC experience *

You will support the production and QA Departments in ensuring all aspects of the manufacture of products are performed in a controlled manner, meeting commitments to international regulatory bodies, as well as Good Manufacturing Practice. Ensure manufactured products are compliant and fit for purpose by performing physical and analytical testing and report accurate results. Duties to include:

• Being responsible for physical analytical testing.
• Follow internal methodologies.
• Adherence to GMP requirements.
• Accurately record microbiological results within data packages, as received.
• Execution of protocols.
• Ensure laboratory housekeeping standards are maintained and documented accurately.
• Ensure all equipment is suitable for use.

The ideal candidate will have the following:

• A relevant BSc degree, eg Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics, or equivalent.
• Be computer literate, with good working knowledge of MS Office.
• Experienced in QC testing of API, including HPLC and GC. Other wet chemistry techniques desirable.
• Good attention to detail, able to prioritise workload, positive and flexible approach.
• One to two years' experience in a similar role would be ideal, but not necessary.
• GMP experience would be desirable.

CVs in Word please.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975. Committed to diversity, equality and opportunity for all. s.mcdermott@newappointmentsgroup.co.uk

This position is part of the Quality Control Department reporting to the QC Manager and will be located in Benoi, Singapore.

In this role, you will have the opportunity to:

• Carry out day-to-day testing including preparation of standards and samples and escalating the failed and risky products.
• Support plant initiatives on PSP, 5S, ESH, Engagement and Kaizen.
• Support to drive lab vision, ensure execution of lab vision to meet company business and production requirement.

The essential requirements of the job include:

• Minimum Diploma in related Science.
• Minimum 3 years of experience in routine QC operations.
• Ability to read/write in English.
• Computer skills – Excel, Word, Typing and Data entry skills.
• Working in 8 hours shift in a cleanroom environment with the gowning procedure.

It would be a plus if you also possess previous experience in:

• Exposure experience to ICP-MS / GC-MS / Liquid Particle Counter/ TOC.
• Good understanding of GMP, GDP, GLP and Quality parameters in QC operations.

Pall Corporation, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.

Have an eye for detail and like to ensure product quality? Come join our team as a QC Lab Analyst if you enjoy quality control and laboratory analysis.

Job Description

· Performing various laboratory tests: routine or non-standard

· Monitoring product quality compliance, from identifying OOS, deviations and quality issues

· Assisting in maintaining laboratory operations: from following the organisation's operational models to reporting any testing activities and results.

· Supporting internal and external audits that occur

Job Requirements

· Minimum a diploma or degree in a science related field

· Attention to detail

· Ability to work with others or independently

Interested Candidates, please forward your updated resumes to:

Audrey Chan Yu Jing – R1104782 at biomedical@recruitexpress.com.sg

EA License No: 99C4599

Please do not use Quick ApplyAll candidates’ informations will be treated with the strictest confidence

EA Personnel No: R1104782

EA Personnel Name: Audrey Chan Yu Jing

about the company
Our client is a renowned insurance firm in Singapore. They are now looking for a Compliance Assurance Analyst (AML) to be responsible for supporting customer on-boarding operations and Anti-Money Laundering functions.

about the job

• You will be responsible for conducting thorough reviews, assessments, and audits to assess compliance levels and identify areas for improvement.
• Perform comprehensive reviews of business operations, processes, and procedures to ensure compliance with applicable laws, regulations, and internal policies.
• Assist in name screening and Anti-Money Laundering support.

about the manager/team
This role lies within the Operations team.

skills and experience required

• Minimum Bachelor's degree in Business Administration, Finance, Law, or related field.
• Proven experience in compliance or operations roles within the financial services industry, especially in the banking or insurance sector.

Role Purpose

The Quality Specialist will be primarily responsible for performing Quality transaction monitoring across the SMB Programs for internal stakeholders as well as external vendors in APAC.

Ideal candidates will need to be proficient in both Customer Service and Sales environments as well as have a good understanding of the APAC market nuances in the specific market he/she is supporting. Success in this position requires strong critical thinking and problem-solving skills and the ability to thrive in a dynamic and changing environment.

Responsibilities:

• Perform audits on recorded client interactions and provide evaluation feedback through QMS
• Conduct regular 1:1 or group calibration to ensure evaluations are aligned based on business requirements.
• Support the business in managing and implementing Quality Management standards and processes that are aligned with the global standard and relevant to the local market nuances
• Highlight trends and red flags to the business for better improvements
• Ensure accurate maintenance of sample calls/chats library
• Provide a bi-weekly QA dashboard highlighting QA audit completion and QA trends to all stakeholders.

Requirement

• Degree preferred or equivalent practical experience;
• Minimum of 2 years of Quality auditing experience in a call centre environment
• Has a clear understanding of the Call Center’s quality framework and methodology.
• Excellent interpersonal and communication skills.
• Bilingual - Fluent in English and one other APAC language (Mandarin and Bahasa Indonesia)
• Self-motivated, entrepreneurial, and comfortable dealing with ambiguity.
• Ability to work in a fast-paced environment.
• Strong attention to detail.
• Coaching experience is a plus
• Knowledge of digital advertising is a plus
• Experience in performing Root Cause Analysis/drill-down is a plus

About Blue Altair:

Have you ever wanted to be a part of something bigger than yourself?

At Blue Altair, we believe each of our employees is a star, full of diverse elements that emit a brilliant light. Just as stars illuminate the night sky, our team members light up the business and technology world with their talent, creativity, and dedication.

Blue Altair is an industry-recognized consulting firm and a trusted partner in digital transformation. Founded in 2015, our services span Assessment and Strategy, Technology Implementation, and Managed Services in API Management and Integration, Data Management, Digital Application Development, and Data Science and AI. We are proud to exceed industry standards for project success, thanks to our expert focus on program and project management, business analysis, and quality assurance.

Working at Blue Altair means being part of a vibrant, dynamic team driving digital change. No matter the role you fill, you'll contribute to the digital future and make a difference. So, if you're a star ready to shine brighter, we can't wait to meet you.

Join us at Blue Altair, where we're not just transforming businesses, but shaping the digital universe one star at a time. Apply now to join our constellation of stars!

Key Responsibilities include:

• Must have good understanding and experience in designing and developing API testing strategies, test cases designing.

• Select appropriate test automation tools, applying the latest techniques and execute test cases in different test environments.

• Must have good experience in developing/executing automated test scripts and setting up the environment.

• Good knowledge of Agile-Scrum methodologies.

• Strong knowledge of JIRA.

• Good understanding of managing test suites and test documentations.

• Actively participated in analyzing and verifying the best automated and manual test approaches and in various testing stages during development/deployment and production release.

Education and Experience Required:

• Bachelor’s or master’s degree in computer science or relevant experience.

• Strong communication skills.

• Testing/Automation certification is highly desired.

In addition to a competitive compensation package, we offer abundant opportunities for you to achieve, excel, and surpass even your own expectations. Aligned with Blue Altair's challenger ethos, we present the Star Elements program, inspired by the composition of stars themselves—comprising diverse elements that give unique qualities and illuminate for thousands of years. Likewise, our initiative aims to facilitate brilliance in our employees. The Star Elements program encompasses a range of benefits, supporting our team across four pivotal facets of their lives and careers. Through Star Elements, our employees can fully realize their potential, both on personal and professional fronts.

• Responsible for maintaining NCR.
• Perform verification of raw material.
• Reviewing and verifying process travelers sequences.
• Supporting quality inspectors.
• Interfacing with engineering, project management and operations to ensure transfer to production of new and existing products are in accordance with approved data.
• Assist quality management in establishing, implementing, and maintaining the quality system.
• Creating inspection and test plans.
• Participating in root cause analysis and implementing of corrective actions.
• Ensuring timely resolutions of supplier failure, corrective actions and preventive actions.
• Analyzing failures, corrective and preventive actions.
• Participating in continual activities to enhance activities of the quality program.
• Conducting audits including closing out audit findings.
• Participating in continuous improvement effort.
• Preparing QA reports.
• API Q1 and Q2 certification is a must.

Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.

This opportunity is for a Senior QC Analyst to join the QC Technical Services Team on a contract basis. The duration of the contract will be 23 months.

Your Responsibilities

You will:

Ensure effective troubleshooting of equipment or technique failures and troubleshooting of problems associated with various analytical techniques.
Sample, analyse and release API, drug products, test incoming raw materials and drug packaging, provide import testing for drug product batches, CDMO batch testing, In process samples, cleaning validation, verification analysis and batch release for raw materials.
Write, review, and drive the completion of validation/analytical transfer activities, owning your analytical projects within the team.
Develop, train and report validation and transfer activities within QC for new and existing clients.
Perform effective reactive and proactive investigations, driving continuous improvements.
Drive compliance working with QA and promote quality standards.
Research, develop, train and report validation and transfer activities within QC for new and existing clients.
Ensure effective troubleshooting of equipment or technique failures and troubleshooting of problems associated with various analytical techniques.
Sample, analyse, and release drug products, test incoming raw materials and drug packaging, provide import testing for drug product batches, CDMO batch testing, cleaning validation, verification analysis and batch release for raw materials.
Write, review, and drive the completion of validation/analytical transfer activities, owning your analytical projects within the team.
Our Company

EUROAPI is focused on reinventing active ingredient solutions to sustainably meet customers’ and patients’ needs around the world. We are a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio, offering a large span of technologies, while developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities.

Taking action for health by enabling access to essential therapies inspires our 3,450 people every day. With strong research and development capabilities and six manufacturing sites all located in Europe (Saint-Aubin-lès-Elbeuf and Vertolaye in France, Brindisi in Italy, Frankfurt in Germany, Budapest in Hungary and Haverhill in the UK), EUROAPI ensures API manufacturing of the highest quality to supply customers in more than 80 countries.

EUROAPI is listed on Euronext Paris.

The EUROAPI Haverhill (UK) site has been established for forty years, located fifteen miles east of Cambridge and sixty miles north of London, within the golden triangle. It employs over 250 people and has built a strong reputation in Flow Chemistry, Active Pharmaceutical Ingredient (API) Spray Drying and as a Contract Development and Manufacturing Organisation (CDMO). Haverhill is proud to house the world’s largest, continuous production, pharmaceutical spray dryer and performs secondary packaging and release activities for oncology and rare disease medicines supporting global markets. The site also offers a contract testing and release facility within its laboratories.

Our Requirements

Sciences degree.

Proven pharmaceutical experience handling HPLC, GC FTIR, UV, PXRD, DSC.

GMP knowledge coupled with proven experience of analytical method validation & transfer principles.

What we offer

Competitive hourly rate and retention bonus
Training & development
A quick turnaround with two interviews (teams interview and face to face) and flexibility to offer a quick start date
23 months contract term
36 hours per week, Monday-Thursday 9-5.30pm, Friday 9-4pm
Apply Today!

Find out more about this exciting opportunity, apply today or contact Victoria Barry-Woods.

Proud member of the Disability Confident employer scheme

An exciting opportunity has opened up with an international fintech firm. This firm is looking for an AML/CFT advisory individual to join their compliance team in Singapore. In this role. you will be providing AML advisory to all business lines, conducting investigations on identified customer profiles, suspicious transactions or activities.

This would be a great and rare opportunity for interested individuals to venture into a stable and ever-growing fintech industry. As part of the expansion plans, the firm is interested to bring onboard individuals who are strong in their compliance knowledge, and yet has a entrepreneurial mindset to come up with creative and innovative solutions.

Requirements

• Experienced in filing of STRs & preparing MIS reports required.
• Min 6 years of experienced in EDD or AML investigations
• Additional certification in AML will be advantageous
• Proficiency in Singapore AML/CFT regulations and guidelines
• Ability to communicate in Mandarin and English

If you are interested in this role or would like to have a discussion, please click "Apply Now" or contact siewching@tenten-partners.com

EA Reg. No.: R22111318

EA Licence No. 16S7919

The Opportunity: CSL Behring is a world class manufacturer of blood plasma proteins which are used to treat human immune deficiencies and severe autoimmune diseases. We are looking for an experienced Quality Control Biochemistry Analyst  to join Quality Control (QC) Biochemistry team at Broadmeadows site on a full-time permanent basis. In this varied role and a high-volume lab, you will ensure that all biochemistry tests are carried out safely, efficiently and following approved test procedures, standard operating procedures and the code of Good Manufacturing Practice.
The Role: Reporting to the Team Leader QC Biochemistry and based on site, you will:

Perform routine biochemistry testing including ELISA, electrophoresis, flow cytometry, nephelometry, auto-coagulation, haemagglutination and endotoxin testing;
Ensure equipment and facilities are maintained and calibrated following approved procedures, and perform troubleshooting in the case of equipment malfunction;
Ensure that all records are completed, signed off, entered onto LIMS, filed and archived;
Complete
... Click here to view more detail / apply for Quality Control Biochemistry Analyst

What’s it all about?

The compliance-risk control framework includes financial crime compliance and regulatory compliance. Financial crime focus is on Anti-Money Laundering (AML), Counter Terrorist Financing (CTF), Sanctions & Anti-Bribery and Corruption (ABC), and on the associated Know Your Customer (KYC) and Know Your Customer’s Business (KYC/B) & Counterparty Due Diligence (CDD) obligations  including primarily but not limited to: -

 

•           On-boarding counterparty due diligence

•           Transactional monitoring

•           Sanctions screening

•           Suspicious activity identification, monitoring and reporting

 

What we expect of you, day to day.

• Develop an understanding of Visa Payments business operations and payment processes
• Identify and internally escalate actual or suspected sanctions matches, assisting and supporting other analysts within the team
• Ensure sanction queries are sent in a timely manner in line with our internal SLAs and deadlines set
• Identify trends and use data to suggest improvements to effectively resolve service issues, escalating appropriately.
• Assist with the development of management information in alignment with regulatory and internal policy/risk expectations
• Assist with the review of new controls to mitigate risks and reduce false positives to improve efficiency across the team.

And assist

• Ensuring clients are within legal parameters and not undertaking ML or criminal activities. For example, using screening and monitoring systems to assess client legitimacy.
• Identifying, managing & escalating suspected and actual money laundering, sanctions breaches and fraud cases through the relevant escalation path.
• Ensuring the compliance risk control framework remains aligned with external legislation.
• Conducting and/or overseeing compliance monitoring reviews and audits.
• Promoting and providing advice on best compliance practice within critical business areas.
• Exemplifying the company values and promoting them in all areas of the role, within and without the function.

 

This is a hybrid position. Hybrid employees can alternate time between both remote and office. Employees in hybrid roles are expected to work from the office two days a week, Tuesdays and Wednesdays with a general guidepost of being in the office 50% of the time based on business needs.

• Responsible of handling corporate user access control to the IT systems.

• To provision and de-provision IT systems access to users in accordance with the joiner and leaver process within the agreed KPI.

• Provide support in advisory capacity to IT Support teams, access approvers and audit teams.

• Liaise with System Administrators and Business Owners to understand role composition and profile management of systems.

• Participate in internal and external audits to produce evidence of process control.

• Ensure all access controls and processes are fit for purpose, and to identify opportunities to streamline the current processesand in order to meet the requirements of audit and compliance policies.

• Identify, document, develop and continually improve processes and controls for access to IT systems.

• Support the UAT testing on administration module to ensure new applications are on-onboarded efficiently, role profiles are appropriate and maintained and that general operation of the solution is monitored and maintained.

Job Requirements

• Diploma or Degree in Information Technology or relevant study.

• Individual interested in technology security and compliance.

• Demonstrates ability to manage communications with stakeholders.

• Work closely with Internal Audit, to align plans and strategy.

• Produce and deliver high quality work products including formal deliverables, technical -documentation and reporting.

• Relevant experience in access control and MS office product.

• Must maintain a strong understanding of access control policies/procedures, vendor onboarding processes and access management resources.

• Review request – Task System and the e-workflow tool.

• Strong discipline in compliance and security policies.

• Good system knowledge relating to workflow, SNOW and access control, or any of the relevant tools.

• Basic knowledge in desktop computing and Microsoft Office products.

For more information, please visit to www.gmprecruit.com and search for Job Reference: 20966
We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | Tang Lee Ling | Registration No: R1106845

Key Responsibilities:

• Establish controls and compliance checks on System Development Methodology (SDM) processes.
• Design, formulate and enforce governance & compliance process improvement.
• Conduct quality gate review for SDM major milestones (analysis, design, build, test and deployment).
• Perform walkthroughs and interviews with project and application delivery managers to drive process adherence.
• Report findings and provide consulting support in ensuring compliances with procedures.
• Aside from day-to-day duties, there will be requirements to undertake other responsibilities such as management reporting & other centrally driven project initiatives as needed.

Key Requirements:

• Degree in computer science/engineering or related disciplines.
• At least 6 to 9 years of relevant experience in IT process compliance audit or Project Management.
• Excellent written and verbal communication, interpersonal, organization and analytical skills a MUST.
• Strong working experience with MS Office (Word, Excel, PowerPoint), MS Visio, MS Project and SharePoint.
• Prior experience in IT risk management and security will be added advantage.

QC lab analyst (Micro)
12 months contract
Salary: Up to $2400 + $400 (Allowance)
Shift: Office hours, Monday-Friday

Location: Tuas

Job Summary:
Conducts Quality Control (QC) inspections on products, materials, components, parts, etc., at various stages of the production process to ensure compliance with established quality and reliability standards. Recommends new or enhanced methods, procedures, and standards. Individual should have a continuous improvement mindset and constantly seek to improve Lab operation processes.

Job Description:

• Ensure timely testing of Environmental and Personnel Monitoring, Stability, Utilities, Components, Raw Materials, and finished product samples, and timely records review as per GMP requirements.
• Assist in investigation on laboratory equipment failure, excursions, Out of Specifications, and any other Non-Conformance Investigation.
• Perform laboratory data trending and escalate any adverse trends accordingly.
• Ensure general laboratory cleanliness and maintain excellent laboratory housekeeping.
• Prepare, support, and front internal or external audits in shaping a successful audit outcome.
• Ensure no critical observation from HA audit.
• Perform any other duties assigned.

How to Apply: send your resume and indicate role(s) you want to apply to: jocelynchan@recruitexpress.com.sg or telegram @jocelynchan
ASAP!

Jocelyn Chan| Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience) Company EA Licence number : 99C4599 Personnel EA License: R1331820

Responsibilities:

• Ensure business operations are following applicable laws and corporate guidelines.
• Conduct investigation and due diligence check on company practices.
• Ensure company practices are adhere to relevant standards.
• Identify, address and resolve business operational issues arise
• Provide business compliance support to sales department and work cross functionally to ensure compliance.
• Stay up to date with trends & latest practices and inform stakeholders and management.
• Oversee the company's business and sales operations.
• Generate data analysis reports for managers to aid in strategic decision-making.
• Implement the risk audit team's recommendations.
• Enhance and include pertinent business conduct and rules initiatives.
• Provide training programmes based on the company's rules of conduct and values.
• Provide guidelines and ensure internal and external stakeholders are following the company's conduct, policies, guidelines, and ethical standards.
• Create and implement procedures for tracking and evaluating adherence.
• Ad hoc duties assigned.

Requirements:

• Bachelor in Business Administration, Finance, Risk Management, Audit or equivalent.
• At least 3 - 5 years of business compliance with data analysis skills.
• Able to work independently will be an added advantage.

Interested candidates who wish to apply for the advertised position, please send in your resume to gs1@talenttradersg.com.

EA License No: 13C6305

Reg. No.: R24120209

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.