Specialist QA Job at Cencora (Juncos)

Specialist QA

Perform one or more of the following duties and responsibilities in support of Q...

Location

United States , Juncos

Salary:

Not provided

Cencora

Expiration Date

Until further notice

Requirements

Doctorate degree or Master's degree and 3 years of directly related experience or Bachelor's degree and 5 years of directly related experience or Associate's degree and 10 years of directly related experience or High school diploma / GED and 12 years of directly related experience
Experience in Quality and Compliance, experience with validation protocols and reports for clean utilities, manufacturing processes, cleaning processes, equipment, computerized systems, change control records, deviations, etc.
Experience in biological processes desired
Project management skills
Strong organizational skills, including ability to follow assignments through to completion
Initiate and lead cross functional teams
Enhanced skills in leading, influencing and negotiating
Strong knowledge in area of expertise
Collaborate and coordinate with higher level outside resources
Strong knowledge of and experience with processes involved in manufacturing and distribution, QA, QAL, validation and process development

Job Responsibility

Review and approve product MPs
Approve process validation protocols and reports for manufacturing processes
Request Quality on incident triage team
Approve Environmental Characterization reports
Release of sanitary utility systems
Approve planned incidents
Represent QA on NPI team
Lead investigations
Lead site audits
Own site quality program procedures

What we offer

medical
dental
vision care
comprehensive suite of benefits focusing on physical, emotional, financial, and social aspects of wellness
support for working families (backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, paid caregiver leave)
training programs
professional development resources
opportunities to participate in mentorship programs, employee resource groups, volunteer activities

Fulltime

QA Specialist (In-Home Care QA visits)

This position will be responsible for conducting in-home visits at clients' home...

Location

United States , Truth Or Consequences

Salary:

Not provided

Arcadia Home Care and Staffing - an Addus family company

Expiration Date

Until further notice

Requirements

Minimum of 3 years’ experience working in the field of senior services or a related social service field
Excellent oral and written communication skills
Strong interpersonal skills
Ability to prioritize and handle high call volumes
Client-focused and customer service-driven
Proficient in Microsoft Word, Excel, and Outlook
Must have reliable transportation, valid driver’s license and insurance for travel within the branch service area

Job Responsibility

Monitors client’s condition and performance of duties by Home Care Aides
Maintains all company and Department on Aging rules, regulations, and standards
Conducts home visits to new clients to welcome and review the Welcome Packet
Observes and evaluates Home Care Aides in the client's home as directed by Supervisor, to assure client Care Plans are being followed
Prepares and completes accurate evaluation reports and case notes as needed
Maintains schedules to assure timely completion of all assigned home visits
Attends weekly branch meetings
Maintains a high degree of confidentiality at all times due to access to sensitive information
Maintains regular, predictable, consistent attendance and is flexible to meet the needs of the department
Follows all Medicare, Medicaid, and HIPAA regulations and requirements

What we offer

Medical, Dental and Vision Benefits
Company matched 401K
Continued Education
Bonus
PTO Plan
Retirement Planning
Life Insurance
Employee discounts

Fulltime

Qa specialist i

We are seeking for a Chemist and detail-oriented QC Technician. As a part of Phi...

Location

Philippines , Biñan

Salary:

Not provided

Sensient Technologies Corporation

Expiration Date

Until further notice

Requirements

bachelor’s degree in related fields plus extensive quality control experience in a commercial or manufacturing environment
knowledgeable of process/ instrument and equipment validation
knowledge in spectrophotometer/ colorimeter and microbiological laboratory is a plus
understands and can use basic statistical tools – Pareto Analysis, Control Charts, Correlation and Regression Analysis, etc.
comprehensive understanding in implementing ISO 17025 and conducting basic physico-chemical testing
familiar with JDE IT or other ERP system will be an advantage

Job Responsibility

routine testing per QC methods and protocols, including designing, conducting and analyzing measurement systems analysis
solve issues and analyze possible solutions using standard procedures, as well as participate in Formal Root Cause Analysis and implement corrective actions
use strong communication skills verbally and in writing to communicate internal lab data across departments and build relationships with teammates
be part of Food Safety team during Quality Audits to ensure positive outcome

What we offer

competitive pay
career advancement opportunities
opportunity to collaborate with colleagues onsite 5 days per week
thorough and constructive training experience during onboarding and beyond
shuttle bus various pick-up points within the city - Alabang & Pasig, nearby Laguna area

Fulltime

Specialist QA, Global Supply Quality

In this role you will be serving patients through internal collaboration with Am...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree with 10 years of experience in manufacturing and quality management systems or a related field OR Bachelor’s degree with 12 to 13 years of experience in quality management systems or a related field
Minimum of 10 years working in a cGMP manufacturing environment with a strong understanding of regulatory requirements and expectations

Job Responsibility

Periodic review and updates to quality agreements to ensure alignment to Amgen expectations and to address needs depending on material type
Documentation review and approval including: supplier manufacturing records, investigation reports, Amgen quality records, and validation records (process & analytical)
Evaluation and documentation of raw materials and devices for changes to incoming inspection profiles
Oversight and completion of supplier assessments and documentation to support product complaints
Ownership of supplier metrics, performance assessments, and other key documents to inform the health of supplier relationships
Review and approval of change control records for supplier changes
Management of supplier audit records, ensuring on time completion and CAPA closeout activities are documented with appropriate closeout evidence
Prepare, review and approve SOPs and other GMP/GDP documentation in compliance with corporate and regulatory requirements, to ensure alignment with procedures, current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations
Take part in operational and quality improvement initiatives, programs, and projects
Develop solutions that are thorough, practical, and consistent with functional objectives

Fulltime

Cdd KYC Qa Specialist

This is Adyen: Adyen provides payments, data, and financial products in a single...

Location

Netherlands , Amsterdam

Salary:

Not provided

Adyen

Expiration Date

Until further notice

Requirements

3+ years of experience in CDD/KYC operational, QA, or compliance control oversight roles
Deep-seated understanding of AML/CFT frameworks and the regulatory nuances governing merchant onboarding and the wider customer lifecycle (including EDR and Terminations)
Exceptional English communication skills
Strong data analysis skills and the ability to synthesize complex information
Track record of working successfully cross-functionally with diverse stakeholders to drive various initiatives and process improvements to completion
You don’t just 'check' work—you own the outcome
You have an 'automation-first' mindset, naturally spotting manual bottlenecks and challenging existing processes to find a better way

Job Responsibility

Perform in-depth QA reviews with a core focus on CDD/KYC processes to identify systemic weaknesses before they become risks
Provide quality oversight as needed across other critical stages of the merchant risk lifecycle, including AML, Screening, Event Driven Reviews (EDR), and Terminations
Maintain the highest quality standards for merchant risk assessments, from initial Underwriting to periodic and event-driven reviews
Develop and maintain clear QA guidelines for analysts, ensuring that quality benchmarks are transparent, easily accessible, and strictly aligned with our global compliance procedures
Design and refine end-to-end QA frameworks that don’t just find errors, but actively facilitate the efficiency and accuracy of our operations
Coach MOPs leads and analysts to take ownership of their own quality
Translate QA findings into actionable dashboards and reports for leadership and compliance functions
Partner closely with 1st line, Compliance, Project Managers (Excellence team), and Product to drive continuous improvement and foster a global culture of shared quality and accountability

Fulltime

Specialist QA - Major Deviations

Let’s do this. Let’s change the world! In this vital role, you will serve as a Q...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master's degree and 2 years of Manufacturing Support and/or Quality Assurance experience OR Bachelor's degree and 4 years of Manufacturing Support and/or Quality Assurance experience OR Associate's degree and 8 years of Manufacturing Support and/or Quality Assurance experience OR High school diploma / GED and 10 years of Manufacturing Support and/or Quality Assurance experience

Job Responsibility

Provide Quality oversight to ensure clinical and commercial pharmaceutical products are manufactured, tested, stored, and distributed in compliance with cGMP and applicable regulations
Serve as Quality investigation lead and decision-maker for complex Major Deviations, maintaining accountability for investigation quality, timelines, documentation, and closure
Actively participate in deviation and RCA meetings, managing multiple concurrent deviations and driving effective resolution
Conduct thorough root cause investigations, including floor presence, process observation, and personnel interviews across shifts, including nights when required
Review, approve, and track cGMP documentation, including Deviations, CAPAs, CAPA Effectiveness Verification (EV), Change Controls, validations, and associated records
Demonstrate strong critical thinking skills, the ability to distinguish causal factors from root causes, and the ability to evaluate investigation quality using evidence-based decision making
Ensure that changes with potential impact to product quality are properly assessed and documented per established procedures
Verify that deviations from established procedures are investigated, documented, and resolved in accordance with Quality System requirements
Ensure production records, laboratory results, and investigation documentation are complete, accurate, and compliant with cGMP standards
Collaborate cross‑functionally with Manufacturing, Engineering, Validation, and Quality to implement effective and sustainable CAPAs

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
Retirement and Savings Plan with generous company contributions
Group medical, dental & vision coverage
Life & disability insurance
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown

Fulltime

Associate Principal QA Specialist

Provide QA review and oversight for various studies and activities. Support a cu...

Location

United Kingdom , Slough

Salary:

32.76 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Education/Degree: Field of Study Scientific
Work Experience: Quality (QA or QC) Level- Advanced - 5-10 years
QA Manufacturing experience
TrackWise records experience (Deviations, Change controls, CAPA's, investigations)
OOS investigations

Job Responsibility

Provide QA review and oversight for various studies and activities
Support a culture of quality and continuous improvement within QC and Development Services
Support Operations to ensure ongoing compliance with GMP
Manage and support GMP issues through QMS processes, site governance and senior QA leadership
Act as a GMP Subject Matter Expert (SME) by implementing, managing and enforcing quality processes on site
Support senior QA leadership in driving continuous improvement and ensuring processes are 'fit for purpose'
Ensure compliance with GMP requirements within Development Services
Maintain compliance with Regulatory Authority expectations, Global Quality Standards and customer requirements
Provide shoulder-to-shoulder review, approval and support for deviations, CAPAs, change controls, investigations and OOS records
Review QA activities for MSAT studies, pilot studies, and Development Services

Fulltime

Lead QA Specialist

The Lead Quality Assurance Specialist in software engineering will lead the QA f...

Location

Malta , Mriehel

Salary:

Not provided

Deloitte

Expiration Date

Until further notice

Requirements

Proven experience leading QA/Testing in software engineering environments, with end‑to‑end ownership of QA outcomes
Strong knowledge of software testing principles, methods and types (functional, regression, integration, usability, performance, load, security, UAT support, etc.)
Hands‑on experience designing and executing test strategies, test plans, test cases and test scripts for complex systems and client implementations
Solid experience with test automation concepts and tools (e.g. UI, API and integration test frameworks) and integrating automated tests into CI/CD pipelines
Familiarity with modern engineering practices (Agile/Scrum, DevOps, continuous delivery, etc) and how QA operates within them
Ability to define and govern QA processes, metrics and standards, and to drive continuous improvement across teams
Strong stakeholder management and communication skills, able to challenge constructively and explain quality risks and trade‑offs to technical and non‑technical audiences
Leadership and mentoring skills, including task delegation, coaching, feedback and fostering a culture of ownership and accountability for quality
A degree in computer science or related field
5 years + in software QA

Job Responsibility

Leads and advances the quality assurance function by setting strategy, managing other QA team members, and aligning QA with organizational and project objectives
Develops QA processes and procedures, including standards for testing methodologies and continuous improvement
Prepares comprehensive test plans, strategies, and scripts tailored to client requirements, ensuring coverage of functional, non-functional, and end-to-end scenarios
Manage and mentor any additional QA personnel introduced as the function grows, ensuring effective performance, training, and alignment with QA objectives
Introduce and maintain innovative testing practices such as test automation and selects and administers appropriate QA toolsets
Executes test plans, strategies, and scripts for clients, performing manual and automated testing while tracking defects and reporting results
Reviews test outcomes daily, troubleshoots issues in systems under test, and coordinates regression, UAT, and performance testing
Manages QA-related meetings, and work closely with the software engineers providing feedback to drive timely issue resolution
Onboards innovative testing approaches, such as test automation frameworks (e.g., Selenium for UI/functional tests), CI/CD integration, and AI-driven tools to enhance efficiency and quality
Mentors QA team members and fosters skill development

What we offer

Four-day work week during July and August
Health Insurance cover for yourself and your dependents
Mental health support through sponsored therapy sessions
Hybrid working option
Digital learning, mentoring and regular performance snapshots

Fulltime

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