Process Associate – Quality Assurance Job at InfoMate (Colombo)

Quality Assurance Associate

DCBL is a highly successful business and are one of the market leaders in Debt C...

Location

United Kingdom

Salary:

28000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Familiarity and competency using Microsoft Office (Word, Excel, Outlook) is essential for effective reporting and communication
Excellent verbal and written communication skills, with a strong ability to produce reports, present findings, and deliver feedback
Strong time management skills to manage multiple priorities efficiently and meet deadlines
Ability to work flexibly and adapt to changing circumstances
High attention to detail to ensure the accuracy and compliance of all processes
Ability to solve problems, be proactive and make decisions effectively
Ability to work as part of a team and alone
Ability to multitask in a fast-paced office environment

Job Responsibility

Conduct regular quality monitoring reviews across all business areas to assess the effectiveness of communications and processes
Identify best practice and areas of concern, providing feedback and findings to relevant stakeholders
Analyse results from quality monitoring, identify recurring issues or themes, and determine the root causes
Collaborate with relevant teams to design corrective action plans to improve overall quality
Identify training needs based on the findings from quality reviews and liaise with operational managers and the training department to ensure support is provided to the necessary teams to improve performance
Work closely with the Operational teams to ensure internal processes align with regulations and company standards
Regularly review and update these processes to ensure ongoing compliance
Monitor and assess adherence to customer and regulatory requirements, including identifying data breaches, ensuring objection handling is effective and complaints are managed according to company protocols
Log and report outcomes and trends identified through QA reviews
Conduct detailed root cause analysis and engage with stakeholders to implement necessary improvements

What we offer

Early finish Fridays
Dress Down Fridays
30 days holiday (including Bank Holidays)
Employee Assistance Programme
Newly refurbished offices
Free Mersey Gateway bridge pass
Free parking
Free tea and coffee facilities
Free monthly lunch
Company social events

Fulltime

Senior Associate Quality Assurance

The Senior Associate QA will be required to perform 12-hour shift (rotational ni...

Location

Singapore , Singapore

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Masters Degree OR Bachelor's Degree and 2 years of directly related experience OR Associate's Degree and 6 years of directly related experience OR High School Diploma / GED and 8 years of directly related experience
Preferred 5+ years of relevant work experience in the commercial manufacturing environment within the pharmaceutical / biologics industry and understanding of GMP pharmaceutical production, biological drug substance experience and operation
Experience with batch record review, and quality record support
Experience in pharmaceutical equipment operation, design and control including GMP change control
Experience in providing floor support, troubleshooting unit operations, and resolving and documenting investigations to support cGMP production
Understanding of equipment log review and continuous monitoring requirements
Good communication skills (technical writing and verbal communication/presentation)
Interacts effectively with variety of communication and working styles
Experience with regulatory audits and inspections
Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality

Job Responsibility

Conduct Quality Assurance activities related to quality floor support for solution and equipment preparation, cell culture and product purification & Drug Substance Filling operations
Support of electronic batch record review and approval, change control, investigations and product release
Work in a cross functional team with Process Development, Manufacturing, Supply Chain, Engineering and Facilities to ensure product quality and market supply
Role may include participation in new product introductions, additional equipment, installation commissioning, qualification
Support continuous improving initiatives

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Senior Associate Quality Assurance

As an Applications Managed Services Engineer (L2) at NTT DATA, your primary miss...

Location

Indonesia , Jakarta Selatan

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

Hands-on experience managing platforms, including ErP, Middleware, and other business-critical software
Moderate experience in managed services with knowledge of using ticketing tools like ServiceNow
Ability to handle multiple tasks, execute change management duties, and lead troubleshooting processes effectively
Ability to plan activities and adapt quickly to changing circumstances
Effective communication skills and the ability to work across different cultures and social groups
Active listening skills to understand clients' needs and craft a positive client experience
Capacity to maintain a positive outlook, even in a pressurized environment, and put in extra effort when necessary
A bachelor’s degree in information technology/computing or equivalent work experience

Job Responsibility

Proactively monitor, investigate, and resolve application-based incidents, service requests, and alerts
Handle second-line support with a medium level of complexity, focusing on resolving client requests and issues without breaching any service level agreements (SLAs)
Update tickets with resolution tasks and promptly log incidents
Communicate with other teams and clients to extend support where needed
Execute changes carefully and ensure all changes are properly documented and approved
Work with automation teams to optimize efforts and coach Service desk and L1 teams
Lead initial client escalations for operational issues
Identify problems before they impact client services and contribute to producing trend analysis reports for continuous improvement
Support project work, execute approved maintenance activities, and assist in implementing and delivering disaster recovery functions

Fulltime

Quality Assurance Associate

Based out of Industrial Oils Unlimited, LLC, located in Tulsa, Oklahoma and repo...

Location

United States , Tulsa

Salary:

Not provided

HF Sinclair

Expiration Date

Until further notice

Requirements

One year of experience in a quality assurance position within a manufacturing setting required
H.S. Diploma or G.E.D. equivalent required
Valid driver's license
Proficiency in quality assurance systems and related software tools
Strong analytical and problem-solving skills with the ability to interpret data and make informed, timely decisions
Excellent organizational and time management skills, with the ability to manage multiple priorities in a fast-paced environment
High level of attention to detail and accuracy in inventory tracking, reconciliation, and documentation
Effective basic written communication skills
Ability to apply fundamental mathematical concepts in inventory calculations and analysis
Proficiency in Microsoft Office applications, with strong emphasis on Excel

Job Responsibility

Understands, follows and enforces all established policies, procedures and recognized practices
References Bills of Material against production to ensure quality of product and final packaging
Conducts shipping and receiving inspections
Works closely with production employees to achieve a quality product
Completes reports, related paperwork, and ensure all information is recorded accurately
Performs secondary checks on production processes
Participates in continuous quality improvement projects and other related activities as assigned
Creates, updates and monitors skillset procedures to ensure efficiency, quality, and currency
Performs quality audits on processes throughout the production cycle
Other duties as assigned by management team

What we offer

Medical Insurance
Vision Insurance
Dental Insurance
Paid Time-Off
401(k) Retirement Plan with match
Educational Reimbursement
Parental Bonding Time
Employee Discounts

Fulltime

Quality Assurance Associate

As a Quality Assurance Associate at Sam’s Club Supply Chain, you will play a vit...

Location

United States of America , Fort Worth

Salary:

21.60 - 25.10 USD / Hour

Walmart

Expiration Date

Until further notice

Requirements

6 months experience in Walmart Logistics clerical related responsibilities (for example, filing, data entry) using computer applications (for example, email, spreadsheet, word processing) OR 1 year's experience in clerical related responsibilities (for example, filing, data entry) using computer applications (for example, email, spreadsheet, word processing)

Job Responsibility

Maintain the quality and accuracy of warehouse inventory
Inspect freight and products for correct quantities and conditions
Identify, research, and resolve inventory discrepancies
Prepare, review, and analyze reports using computer applications
Move freight manually and with powered equipment
Maintain a clean work environment to ensure safety and compliance
Comply with company policies, procedures, and standards of ethics and integrity
Perform additional duties as assigned

What we offer

medical, vision and dental coverage
401(k), stock purchase and company-paid life insurance
PTO, parental leave, family care leave, bereavement, jury duty, and voting
short-term and long-term disability, company discounts, Military Leave Pay, adoption and surrogacy expense reimbursement
Live Better U education benefit program

Fulltime

Regulatory Affairs & Quality Assurance Associate

NYES is looking for a motivated, detail-oriented Regulatory Affairs & Quality As...

Location

United States , Brooklyn

Salary:

Not provided

New York Embroidery Studio

Expiration Date

Until further notice

Requirements

Recent Regulatory Affairs and Quality Assurance (RAQA) Graduate Program
1–2 years of experience in a regulated industry (MedTech, Biotech, or Pharma)
Internship experience in RA/QA is highly valued
Understanding of FDA Class I and II medical device classifications
Familiarity with ISO 13485 and 21 CFR 820 frameworks
High level of technical writing proficiency
attention to detail
a "student of the craft" mentality
A clear desire to grow into a leadership role within NYES

Job Responsibility

Assist the Manager in the daily maintenance of the ISO 13485 Quality Management System, including document control and CAPA tracking
Support the preparation of FDA 510(k) premarket notifications and NIOSH approval packets for N95 respirators and surgical masks
Perform routine checks to ensure manufacturing processes align with 21 CFR Part 820 (Quality System Regulation)
Draft and update Standard Operating Procedures (SOPs), labeling, and IFUs (Instructions for Use) to ensure accurate regulatory claims
Work with third-party labs to track ASTM barrier performance testing (fluid resistance, viral penetration) and organize results for regulatory dossiers
Participate in internal audits and assist in preparing the facility for external inspections from the FDA or Notified Bodies

What we offer

Direct Mentorship: Learn from a veteran Lead with 5–10 years of specialized PPE experience
Clear Career Path: This isn’t just a job
it’s a prepared seat
Impact: Your work ensures that frontline healthcare workers receive PPE that is safe, cleared, and effective

Fulltime

Associate Quality Assurance (Incoming QA)

As Associate Quality Assurance, you will be part of the Incoming QA team, playin...

Location

Netherlands , Breda

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

MBO or Bachelor's degree in Life Sciences or a related field, or an equivalent combination of education and experience
Preferably around three years of experience within the pharmaceutical industry or a regulated environment
Working knowledge of Good Manufacturing Practice (GMP) and/or Good Distribution Practice (GDP), with the ability to interpret and apply requirements in routine situations
Strong attention to detail, structured way of working, and a quality-first mindset
Fluency in English, both written and spoken

Job Responsibility

Execute sampling and inspection of incoming materials, including commercial and clinical printed and non-printed packaging components and devices
Perform review and release of incoming materials in accordance with applicable procedures and quality requirements
Collect data and initiate follow-up with internal stakeholders (e.g. Warehouse, Supply Chain, External Supply) and/or Amgen suppliers to resolve quality issues
Initiate, document, and own minor deviations, ensuring timely investigation and closure
Perform reserve sample inspections to support product complaint investigations, deviations, or the annual reserve sample inspection process
Execute additional sampling, inspection, and damage assessment of received components as required

What we offer

Full support and resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising competitive salary, bonus structure, fixed 13th month, holiday allowance and a collective health insurance
Focus on vitality with an on-site gym, vitality program and a restaurant with healthy food

Fulltime

Senior Associate Quality Assurance

The Incoming Quality Assurance (IQA) Associate position will provide support for...

Location

Singapore , Singapore

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Masters Degree OR Bachelor's Degree and 2 years of directly related experience OR Associate's Degree and 6 years of directly related experience OR High School Diploma / GED and 8 years of directly related experience
5 years of experience in regulated environment
Experience and basic troubleshooting skills with laboratory and process equipment
Experience with LIMS, SAP, TrackWise, Veeva
Ability to understand, apply and evaluate basic chemistry
Ability to adhere to regulatory requirements, written procedures and safety guidelines
Ability to evaluate documentation/data according to company and regulatory guidelines
Ability to interact with inspectors (internal and external)
Ability to interpret and apply Good Manufacturing Practice (GMP) knowledge
Ability to organize work, handle multiple priorities and meet deadlines

Job Responsibility

Comply with safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
Complete required assigned training prior to execution of required tasks
Perform raw material inspection, sampling and rapid ID testing in accordance to written SOPs and Methods.
Generate complete and accurate documentation using electronic or handwritten systems.
Review records to ensure raw materials are tested and inspected according to specification and SOPs
Perform business operations related to inspection/sampling/testing (i.e updating dashboards, relevant metrics, housekeeping, inventory management, audit support)
Support site/network Continual Improvement initiatives
Ensures facilities, equipment, materials and procedures comply with cGMP practices and other applicable regulations
Alert management of quality, compliance, supply and safety risks in a timely manner
Participate in raw material issues or deviations

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

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Process Associate – Quality Assurance

Job Description

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