Total 721 analyst job vacancies in Quality Assurance / Control category in The United States of America

We are currently seeking an interim Quality Control Analyst (Scientific), to work with our global FMCG client , renowned for brands such as Dove, Sure, Persil, and Simple, and become an integral part of their fast-paced FMCG environment.

The position is based in Port Sunlight Village, Wirral - easily accessible by train and car. This is a full-time temporary role to run for 12 months, requiring 37.5 hours per week, Monday to Friday 8am - 4pm. Compensation for this role is competitive, paying between £36,577 per annum.

MAIN JOB PURPOSE:

The quality analyst is responsible for routine quality control of raw, intermediate and finished products. The analyst also ensures that any problems or issues are communicated and resolved. The role involves mostly independent working as part of team success and is critical to ensuring that all products that leave the factory meet consumer expectations and safety requirements.

Previous experience in a similar field or a science related degree is preferred, as well as good computing skills and being able to demonstrate an ability to think beyond the immediate next step is a plus

KEY AREAS OF ACCOUNTABILITY:

1. Safety

• Ensure Company safety policy, rules and procedures are understood and followed on all operational tasks and improvements
• Identify and report health or safety hazards and dangerous situations and put appropriate control measures in place
• Perform risk assessments as appropriate
• Prepare, maintain, monitor and lead COSHH assessments (following suitable training) where required

2. Quality

• Perform routine analysis of raw, intermediate, and finished products (chemical, microbiological and enzymatic) following established methods
• Good working knowledge of QC procedures, U/L GMP guidelines, any legal operating standards and assists in training other teams as and when required
• Initiate OOS notifications and follow up investigations
• Perform routine equipment calibration and maintain control charts
• Stock taking and submission of orders for laboratory consumables
• Provide support in hygiene laboratory with sample collection, media preparation, analysis (using established microbiology laboratory methods TVC or ATP) and release of products to market
• Support introduction of new innovations and hygiene validations
• Conduct audits of sourcing unit in different areas (for example CRQS, Environmental, Process, GMP)
• Demonstrate good knowledge and use of SAP system (QM)

3. Customer Service

• Provide advice to Leaders and Management on resolving out of specification results in a timely manner.
• Ensure timely release of product to market, interact with all levels within the Factory

4. 5S

• Perform regular inspections/audits for good housekeeping / 5S and ensure agreed actions are completed
• Ensure 5S standards are clearly defined and followed

5. Effective Maintenance

• Ensure all Laboratory equipment is maintained to the correct working standards.

6. Training and Development

• Ensure technical skills are maintained to current and future business requirements regarding product conformity
• Ensure full compliance with analytical training schedule where applicable

1. Attitude/Effort

• Ambitious to hit personal targets and standards
• Act to remove basic blocks to progress without waiting for others to do it
• Persistent in overcoming obstacles to success
• Highly motivated and committed to their role

2. Safety and Environmental Conduct:

• Actively support a safety environment, reacting quickly to safety incidents
• Follows and contributes to all safety regulations
• Encourages others to behave in a safe manner

3. Self Development and Others:

• Rapidly absorbs new information, knowledge and applies new techniques or procedures
• Pursue new opportunities to develop or enhance own experience and capabilities
• Support the development of colleagues
• Seek feedback from others to further development their own skills & behavior

4. Problem Solving:

• Apply WCM approach to identify and eliminate root causes
• Sees problems through to a complete solution to eliminate the problem
• Use technical skills to solve problems
• Demonstrate an ability to think beyond the immediate next step

5. Team Working:
   • Participate constructively and willingly as a team player - following the team Ways of Working
   • Demonstrate commitment to the team in helping it achieve its goals
   • Adapt own actions for the good of the team
   • Participate constructively and willingly as a team player
   • Proactively share best practice, ideas and insights with colleagues

The Quality Analyst role requires the following specific skills:

• Significant previous experience within a Quality role or a science related Degree (or equivalent)
• Previous experience in Root Cause Analysis and Corrective Action Tools
• Good computing skills

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

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.

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.

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.

• 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

Find Your Dream Job With Us

WE ARE HIRING !! Apply now and make a difference.

Role: Process Assurance Analyst

Job Requisition Number: JR32278

Job Level: Preferably 6 to 9 years of relevant experience (L3)

Location: Singapore

Key Skills: IT Risk Management, Project Management & Business Process Design

Job Objectives

The Process Assurance Team (PAT) is within Global Market and Enterprise Technology (GMET) organization, supporting bank’s Project, Development and Service Delivery teams to ensure process compliance to System Development Methodology (SDM) process

The team acts as a quality gate for SDM major milestones to ensure entry & exit criteria are met and is responsible to review the quality of the artefactsuch as functional & design specification, testing documents and others project deliverables.

The successful candidate will be working with Project and Technical Delivery managers to ensure high quality of deliverables.

Key Responsibilities

l Establish controls and compliance checks on SDM processes

l Design, formulate and enforce governance & compliance process improvement.

l Conduct quality gate review for SDM major milestones (analysis, design, build, test and deployment)

l Perform walk through and interviews with project and application delivery managers to drive process adherence

l Report findings and provide consulting support in ensuring compliance'swith procedures

l 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

l Degree in computer science/engineering or related disciplines

l At least 6 to 9 years of relevant experience in IT process compliance audit, Project Management.

l Excellent written and verbal communication, interpersonal, organization and analytical skills a MUST

l Strong working experience with MS Office (Word, Excel, PowerPoint), MS Visio, MS Project and SharePoint

l Prior experience in IT risk management and security will be added advantage

Please forward your resume in MS word format to Careers@infogainglobal.com and Suganthi@infogainglobal.com

Please refer your friends for any IT openings as we have various positions.

Please do not send PDF Format Resume . Send the following details

1. Notice period

2. Current Salary

3. Expected Salary

4. Visa Status in Singapore

5. Current Location

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.

Who We Are   Downer is the leading provider of integrated services in Australia and New Zealand. Our Industrial & Energy business provides end-to-end facilities management and asset lifecycle support services for Australia’s critical economic infrastructure. Operating across the future energy, power generation, oil and gas and industrial sectors, we work closely with our customers to optimise the reliability, efficiency and whole of life costs of their assets and facilities.    About the Role  We are currently seeking applications from experienced Quality Assurance Advisors to join our Power and Energy business to assist with shutdowns to a market leading client. The QA Advisor will be the onsite focus to deliver QA activities for our alumina refinery project in Yarwun, QLD  About You   A Trade qualification in Fitting or Boilermaking highly desirable Previous demonstratable experience in a similar role, preferably in a project environment Knowledge of Australian Standards and ISO is preferred Excellent communication skills both written and verbal…

Click here to view more detail / apply for Quality Analyst

Presently we have a Job Opening for a Test Analyst position with one of our leading clients in Singapore

Atleast 4 years hands on experience in Testing
Should have experience in full STLC
Hands on experience in any of the Automation tools
Good communication & written skills

Should be ISTQB Certified

Join Our Team at a Leading Pharma MNC!
Position: QC Analyst (6-month Contract)
Location: Tuas
Salary: Up to $3,200 per month

Job Description:
We are hiring a QC Analyst for a 6-month contract at our prestigious pharmaceutical MNC. This role involves performing quality control testing and analysis to ensure product compliance and quality standards.

Key Responsibilities:
Conduct quality control tests on raw materials, intermediates, and finished products.
Analyze and interpret test results accurately.
Maintain laboratory documentation and records.
Adhere to Good Manufacturing Practices (GMP) and safety guidelines.

To Apply: Send your resume to Jocelynchan@recruitexpress.com.sg or telegram @jocelynchan

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

Jiteraについて

Jiteraは、モバイルおよびWebアプリケーションの開発自動化を可能にする、生成AIを用いたローコード・ノーコードプラットフォームを開発している日本発のスタートアップ企業です。

Jiteraの開発自動化プラットフォームを使用することで、ソフトウェア開発を10倍速く行うことができます。

開発中で試行錯誤が絶えないですが、当社のプラットフォームで開発されるアプリケーションは増えています。通常のコーディングをゼロから行う場合と比べて、10倍速くモバイルアプリケーションが開発されたケースもあります。

Jiteraはフルリモートでグローバルな組織です。様々なチャレンジのもと、過去1年間で収益、チーム、提供できるサービス価値など、多くの面で成長を遂げてきました。

このポジションについて

当社の製品品質の維持と向上を担うシニアQAアナリストとして、開発されるシステムが正しい機能を備えており、要件仕様に準拠していることを保証する責任を負います。品質基準に適合するようにテスト戦略を立案し、実行することで、ユーザーに高品質な体験を提供することが求められます。

また要件定義フェーズよりプロジェクトマネージャーと伴走し、要件の理解を深めつつ、プロジェクトマネージャーをサポートする業務にも携わります。

主な業務内容

• 探索的テストによるシステムのバグの特定、報告、追跡
• 要件に従ったシナリオテストの作成、及びそれらの文書化
• テスト活動の実行とテスト結果の評価
• プロダクトオーナーや開発者と連携し、問題解決を行う
• QAプロセスの改善提案と実装

副次的な業務内容（プロジェクトマネージャー補佐）

• ユースケースなど要件定義資料の作成
• 要件定義書やFigma上の画面項目の翻訳（日本語から英語がメインです）
• ドキュメント作成とスケジュール管理（例：ミーティングの議事録、スケジュール等）

必要なスキル・経験

• ソフトウェア品質保証における実務経験
• テストシナリオの作成能力
• 問題の特定、分析、解決能力
• （特にリモートワークで必要となる）高いスピード感覚とオーナーシップ
• 英語でのビジネスレベルの会話能力、あるいは英語を本気で学ぶやる気がある

歓迎されるスキル・資格

• IT業界やソフトウェア開発プロセスの基本的理解
• Agile開発環境での作業経験
• テスト関連資格（例：ISTQB Certification）
• ChatGPT、Open Interpreter、Microsoft Copilotなど、最新の生成AIサービスを使いこなす主体性と知見がある
• リスペクトを持ち、コミュニケーションを大切にしてチームとして成果を出せる人柄

待遇・福利厚生

• フルリモート・フルフレックス
• 社会保険完備
• 完全週休2日制（土日）
• 有給休暇
• 最新モデルのMacBook Pro貸与
• 夏季休暇、年末年始休暇
• ストックオプション制度
• 英語学習プログラム受講支援

1 Year Compliance Analyst (Global Bank)

The position falls within a group of associates in the Anti-Money Laundering Client Due Diligence (AML/CDD) onboarding team. This team primarily focuses on the initiation of new clients and expansion within Global Banking and Global Markets. It involves conducting AML/CDD checks according to country standards and complying with Customer Identification Program (CIP) and Customer Due Diligence (CDD) protocols. The role emphasizes the delivery of seamless service and ensuring client satisfaction.

Job Requirements:

• At least 2-4 years of relevant working experience
• Excellent presentation, communication skills
• Experience in corporate banking industry

Interested applicants please send your resume in MS Words format to Claire.chu@ambition.com.sg and attn it to Chu Chin Siew (Claire) (R1989696)

Short listed candidates will be notified

www.ambition.com.sg

EA Registration Number: R1989696

Data provided is for recruitment purposes only

Business Registration Number: 200611680D. Licence Number: 10C5117