Quality Assurance Associate jobs at CohnReznick - 909 jobs
QC E-File Mailbox Temps
Cohnreznick 4.7
Quality assurance associate job at CohnReznick
As CohnReznick grows, so do our career opportunities. As one of the nation's top professional services firms, CohnReznick creates rewarding careers in advisory, assurance, and tax with team members who value innovation and collaboration in everything they do!
CohnReznick helps organizations optimize performance, manage risk, and maximize value through CohnReznick LLP (assurance services) and CohnReznick Advisory LLC (advisory and tax services). Together, the firm provides leaders with deep industry knowledge and relationships, solutions to address clients' unique business goals and risks, and insight on how emerging market forces can drive opportunity. With offices nationwide, the firm serves organizations around the world as an independent member of Nexia.
We currently have an exciting career opportunity for an QC E-File Mailbox Temp to join the team in our Practice Management practice.
CohnReznick is a hybrid firm and most of our professionals are located within a commutable distance to one of our offices. This position is considered remote which means it does not require job duties be performed within proximity of a CohnReznick office location. However, as a remote employee, you may be required to be present at a CohnReznick office with scheduled notice for client work, team meetings, or trainings.
YOUR TEAM.
This position will support QC e-file mailbox Support- Supporting office's Tax Department on managing the local e-file mailbox on client Tax authorization forms
Hours for positions will be:
8:30am-5pm M-F and evening and weekend OT coverage leading to deadlines
22.5 hours a week starting on 5/16 and brought back up to regular hours on 8/1
WHY COHNREZNICK?
At CohnReznick, we're united by a common mission to create opportunity, value, and trust for our clients, our people, and our communities. Whether it's working alongside your peers to solve a client challenge, or volunteering together at the local food bank, there are so many ways to find your “why” at the firm.
We believe it's important to balance work with everyday life - and make time for enjoyment and fun. We invest in a robust Total Rewards package that includes everything from generous PTO, a flexible work environment, expanded parental leave, extensive learning & development, and even paid time off for employees to volunteer.
YOUR ROLE.
Responsibilities include but not limited to:
Ability to multi-task and turn around projects quickly.
Extensive administrative and computer use.
Dependable, reliable, and a strong attention to detail with the ability to self-review.
Can-do attitude and an ability to work under pressure to meet deadline.
YOUR EXPERIENCE.
The successful candidate will have:
Proficient computer uses in a business environment.
High school diploma or equivalent work experience.
Strong organizational skills; effective communication and interpersonal skills.
Prior experience with Adobe, Caseware, GoFileRoom, CCH ProSystem Scan is a plus!
In addition, please take a moment to review our Universal Job Standards.
Studies have shown that we are less likely to apply to jobs unless we meet every single qualification. At CohnReznick, we are dedicated to building a diverse, equitable, and inclusive workplace, so if you're excited about this role but your experience doesn't align perfectly with every qualification in the job description, we still encourage you to apply. You may be just the right candidate for this or one of our other roles.
In New Jersey, the salary range for a Data Validator is $22 an hour. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. Salary is one component of the CohnReznick total rewards package, which includes a discretionary performance bonus, generous paid time off, expanded and inclusive parental benefits, to name a few. To learn more about life at CohnReznick, visit Life at Life at CohnReznick
"CohnReznick" is the brand name under which CohnReznick LLP and CohnReznick Advisory LLC and their respective subsidiaries provide professional services. CohnReznick LLP and CohnReznick Advisory LLC (and their respective subsidiaries) practice in an alternative practice structure in accordance with the AICPA Code of Professional Conduct and applicable law, regulations, and professional standards. CohnReznick LLP is a licensed CPA firm that provides attest services to its clients. CohnReznick Advisory LLC provides tax and business consulting services to its clients. CohnReznick Advisory LLC and its subsidiaries are not licensed CPA firms.
CohnReznick is an equal opportunity employer, committed to a diverse and inclusive team to drive business results and create a better future every day for our team members, clients, partners, and communities. We believe a diverse workforce allows us to match our growth ambitions and drive inclusion across the business. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information, please see Equal Employment Opportunity Posters.
If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at CRaccommodation@CohnReznick.com Please note: This email address is reserved for individuals with disabilities in need of assistance and are not a means of inquiry about positions or application statuses.
CohnReznick does not accept unsolicited resumes from third-party recruiters unless such recruiters are currently engaged by CohnReznick Talent Acquisition Team by way of a written agreement to provide candidates for a specified opening. Any employment agency, person or entity that submits an unsolicited resume does so with the understanding that CohnReznick will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity.
#LI-CM1 #GD #IND123
$22 hourly 4d ago
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Biopharma Manufacturing QA Associate
Yoh, A Day & Zimmermann Company 4.7
South San Francisco, CA jobs
Yoh Life Sciences is hiring for Quality AssuranceAssociate in South San Francisco. You will support day-to-day quality operations and ensure compliance across the manufacturing processes. This role provides hands-on QA support on the production floor, assists with document control activities, and works closely with Manufacturing, Warehouse, and Quality Control teams to maintain high standards of product quality and cGMP compliance.
Title: QA Associate
Location: South San Francisco - must be local to the area
Schedule: M- F 8-5pm with flexibility during manufacturing runs
Industry: Biotech/CDMO/Cell Therapy
Pay: $35-$40/hr W2
Responsibilities
Provide QA support for daily manufacturing operations in accordance with approved SOPs and cGxP requirements.
Assist in reviewing executed batch records, logbooks, and production documentation for accuracy, completeness, and cGMP compliance.
Support deviation initiation and investigation activities, including documentation, root cause analysis, and timely closure.
Assist with material release.
Perform routine QA walkthroughs on the manufacturing fl oor and escalate quality events per established procedures.
Support document control activities, including the review and routing of SOPs. ? Participate in change control processes for operational and documentation changes.
Support quality oversight of product status, including shipping documentation and release readiness.
Identify and help correct non-compliance with cGMP and GDP requirements.
Perform other QA-related duties as assigned to support operational needs.
Requirements
Bachelor's degree in a related fi eld (e.g., Life Sciences, Engineering, Quality Assurance, etc.)
1-5 years of experience in quality management or quality assurance, preferably in a regulated industry (e.g., medical devices, pharmaceuticals, cell & gene therapy, etc.)
Basic understanding of cGMP principles and regulatory requirements (FDA, EMA, ICH).
Familiarity with quality management systems and GDP practices in a GMP facility.
Experience in cell therapy or cell-based manufacturing is a plus.
Excellent communication, organizational, and analytical skills in a fast-paced, dynamic environment.
#IND-SPG
Estimated Min Rate: $35.00
Estimated Max Rate: $40.00
What's In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
Health Savings Account (HSA) (for employees working 20+ hours per week)
Life & Disability Insurance (for employees working 20+ hours per week)
MetLife Voluntary Benefits
Employee Assistance Program (EAP)
401K Retirement Savings Plan
Direct Deposit & weekly epayroll
Referral Bonus Programs
Certification and training opportunities
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************
$35-40 hourly 5d ago
Mainframe QA Analyst
Highbrow LLC 3.8
Morris Plains, NJ jobs
Job Title: Mainframe QA Analyst
Job Travel Location(s):
# Positions: 3
Employment Type: W2
Duration:Long Term
# of Layers:0
Work Eligibility:All Work Authorizations are Permitted - No Visa Transfers
Key Technology:COBOL, JCL, DB2, CICS
Job Responsibilities:
Ensure the quality and functionality of mainframe systems and applications, primarily working on COBOL, JCL, CICS and DB2.
Design and execute test cases, analyze requirements, troubleshoot issues and improve performance.
Develop detailed test cases and test data based on requirements, conduct manual testing focusing on functional, integration, regression and system testing.
Execute test cases on mainframe environments and validate data accuracy in DB2.
Log, track the defects and perform Root cause analysis of the defect.
Collaborate with cross functional team
Prepare and present the test results and metrics.
Skills and Experience Required: Required:
3 -5 years of experience in Mainframe QA activities
Knowledge of COBOL, JCL, DB2, CICS
Experience in working with large data sets, data validation and SQL queries
Familiarity with mainframe testing tools - automation testing
Knowledge of test management tools - JIRA
Work experience with Agile methodologies and scrum framework
Good analytical skills and attitude to learn newskills
Problem solving and troubleshooting skills
Strong communication and Interpersonal skills
Ability to work independently and as a team.
Education:
Bachelor's degree in related field or equivalent work experience.
#J-18808-Ljbffr
A technology company in Morris Plains, NJ is looking for a Mainframe QA Analyst to ensure the quality of mainframe systems. The role requires expertise in COBOL, JCL, DB2, and CICS, alongside 3-5 years of mainframe QA experience. Candidates should have strong analytical skills and experience with test management tools like JIRA. The position calls for both independent and collaborative work, emphasizing problem-solving and communication skills in a fast-paced environment.
#J-18808-Ljbffr
$70k-93k yearly est. 4d ago
Associate, Quality Operations QA
Talentburst, An Inc. 5000 Company 4.0
Norton, MA jobs
Industry: Pharmaceuticals
Title: Associate, Quality Operations QA
Duration: 09 months contract (+Possibility of extension)
Onsite with 1x per week flexibility as needed.
About the Role
The QA Associate will help ensure that life-changing biopharmaceutical products are manufactured to the highest standards. The QA Associate will provide day-to-day QA support across manufacturing, validation, materials, QC, engineering and facility operations at our Norton site, partnering with cross-functional teams to maintain GMP compliance and inspection readiness.
Key Responsibilities
Provide raw material support, including review/approval of incoming material documentation and release for GMP use.
Deliver on-the-floor QA support to manufacturing, including area clearance and changeover operations, ensuring readiness for production activities.
Review and approve SOPs, master batch records (MBRs), specifications, risk assessments, and quality documents.
Generate and maintain Quality-related SOPs and controlled forms.
Review and approve validation documents and protocol executions to confirm compliance with approved procedures and regulatory requirements.
Review and approve QC laboratory qualification documents, including equipment qualification.
Perform executed batch record review and approval to ensure accuracy and compliance.
Review and approve deviations, CAPAs, Change Controls and related investigations in the quality management system.
Support partner audits and regulatory inspections, including document retrieval and subject matter input.
Approve work orders in the maintenance system to verify equipment maintenance and calibration compliance.
Collaborate with internal cross-functional teams at the Norton facility to drive continuous improvement and quality excellence.
Qualification/Skills
Bachelor's degree in a scientific or engineering discipline (Biology, Chemistry, Biotechnology, etc.) or equivalent experience.
2-4 years of GMP experience in Quality, Manufacturing, or QC.
Knowledge of cGMP regulations (21 CFR Parts 210/211/11, ICH Q7/Q10) and Good Documentation Practices.
Strong attention to detail, organizational skills, and the ability to communicate effectively across teams.
Experience with quality systems (e.g., Veeva, SAP) is a plus.
$57k-71k yearly est. 1d ago
Quality Assurance Specialist
Cypress HCM 3.8
Tustin, CA jobs
This is an exciting opportunity to join a growing company that focuses on precise, early detection of emerging diseases. The Quality Assurance Specialist ensures products, processes, and documentation meet established quality standards and comply with applicable regulatory requirements. This role blends regulatory submissions and strategy with quality system implementation, auditing, and continuous improvement to support product approvals, market access, and patient safety.
Responsibilities
Develop, implement, and maintain the Quality Management System (QMS).
Plan, conduct, and coordinate internal and supplier audits to ensure compliance with regulatory and accreditation standards (e.g., CLIA, CAP).
Manage document control, change control, CAPA, nonconformance management, complaint handling, and MDR/Vigilance activities.
Coordinate proficiency testing programs and analyze results to identify trends and improvement opportunities.
Ensure all required regulatory licenses and accreditations remain current.
Maintain quality documentation, SOPs, and laboratory testing procedures.
Prepare, analyze, and present quality metrics and reports for management review.
Train and onboard new personnel; review training documentation and monitor ongoing competency of testing staff.
Maintain working knowledge of laboratory protocols, specimen processing, equipment operation and maintenance, and data analysis.
Review and approve product labeling, packaging, promotional materials, and technical documentation for regulatory compliance.
Monitor changes in global regulations, standards, and guidance; assess impact and recommend updates to internal processes.
Partner with cross-functional teams (R&D, manufacturing, engineering, clinical, marketing) to embed quality and regulatory requirements early in product development.
Lead or support management reviews, regulatory and quality training programs, and continuous improvement initiatives.
Prepare, submit, and maintain regulatory filings, documentation, and reports.
Coordinate with regulatory and accreditation bodies to support product approvals, certifications, and inspections.
Ensure compliance with internal health and safety policies; report and address violations as required.
Participate as an external auditor on College of American Pathologists (CAP) inspection teams, as required by the CAP accreditation program.
Requirements And Desired Experience
Bachelor's degree (required) in life sciences, biology, chemistry, engineering, pharmacy, or related field; Master's a plus
3+ years of laboratory experience, including experience with audits, compliance systems, and regulatory submissions.
Strong knowledge of key regulations and standards: FDA QSR (21 CFR Part 820/211), ISO 13485/9001, EU MDR/IVDR, GMP, ICH guidelines, etc.
Working knowledge of relevant regulatory frameworks
Professional certification is a plus (i.e, Regulatory Affairs Certification - RAC, ASQ Certified Quality Auditor - CQA).
CLS Generalist or CGMBS license preferred
Proven knowledge of quality assurance terminology, software, methods, and tools.
Previous experience with Laboratory Information Management Systems is preferred.
Proficient in QMS software (i.e. MediaLab, TrackWise, MasterControl or similar)
Strong analytical, problem-solving, and decision-making skills.
Experience in compliance and/or regulatory and knowledge of laboratory standards and regulations
Experience with Microsoft Office Suite; Word, Outlook, Excel
Excellent written and verbal communication skills for agency interactions, technical writing, and cross-functional collaboration.
Able to effectively present information and respond to questions from various stakeholders
Compensation (DOE): $80,000 - $95,000 annual salary
$80k-95k yearly 4d ago
Quality Assurance Tech II: 26-00078
Akraya, Inc. 4.0
Boston, MA jobs
Primary Skills: Robotics testing (Expert), Automaton Testing (Proficient), Documentation (Proficient), Test Plans (Proficient), bug management (Proficient), Contract Type: W 2 Duration: 6 months with possible extension Location: Boston, MA (#LI-Onsit Quality Assurance, Assurance, Tech, Test Engineer, Staffing, Product Development, Business Services
$35k-43k yearly est. 8d ago
Quality Assurance Tech II: 26-00078
Akraya, Inc. 4.0
Boston, MA jobs
Primary Skills: Robotics testing (Expert), Automaton Testing (Proficient), Documentation (Proficient), Test Plans (Proficient), bug management (Proficient), Contract Type: W2 Duration: 6+ months with possible extension Pay Range: $45.00 - $50.00 per hour
#LP
Job Summary:
We are looking for a Quality Assurance Technician II to join our team, dedicated to operating and supporting robotic technology at sortation centers. This role involves executing test plans, collecting and analyzing data, and reporting results under the guidance of Test Engineers and Engineering Leads. The successful candidate will work closely with sortation center personnel to ensure the successful integration of new technologies into our product development process.
Key Responsibilities:
Execute test plans developed by Global Engineering Test Engineers.
Collect and analyze data from testing processes to identify areas for improvement.
Engage with Test Engineers, TE Manager, and Engineering Leads for guidance and direction.
Collaborate with local sortation site personnel including Operations, RME, WHS, etc.
Report results and findings to stakeholders and suggest recommendations for enhancements.
Must Have Skills:
Operate and test robotic technologies at sortation centers, supporting onboarding into RDPI's product development process
Execute engineering test plans and test cases developed by RDPI Global Engineering Test Engineers
Collect, analyze, and report test data and results with accuracy and clarity
Work under direct guidance from Test Engineers, TE Managers, and Engineering Leads to support testing objectives
This role offers the chance to work with cutting-edge robotic technologies and contribute to the development of new processes within a leading global company. If you are passionate about quality assurance and have a knack for working with innovative technologies, we'd like to hear from you.
ABOUT AKRAYA
Akraya is an award-winning IT staffing firm consistently recognized for our commitment to excellence and a thriving work environment. Most recently, we were recognized Inc's Best Workplaces 2024 and Silicon Valley's Best Places to Work by the San Francisco Business Journal (2024) and Glassdoor's Best Places to Work (2023 & 2022)!
Industry Leaders in IT Staffing
As staffing solutions providers for Fortune 100 companies, Akraya's industry recognitions solidify our leadership position in the IT staffing space. We don't just connect you with great jobs, we connect you with a workplace that inspires!
Join Akraya Today!
Let us lead you to your dream career and experience the Akraya difference. Browse our open positions and join our team!
$35k-43k yearly est. 8d ago
Quality Assurance Engineer
The Intersect Group 4.2
Irving, TX jobs
A client of The Intersect Group is seeking a seasoned Quality Assurance Engineer with deep experience in retail systems and end‑to‑end retail operations. In this role, you'll ensure that globally deployed applications meet high bars for functionality, reliability, and performance across multiple regions and languages. Your work will directly improve product quality and speed to market, elevating customer experience and operational efficiency.
You will design and execute both manual and automated tests across mobile, web, and backend services, partnering closely with product managers, designers, and engineers. You will manage testing across environments, track issues through resolution, report meaningful quality metrics, and actively shape test strategies and standards that scale across teams.
Key Responsibilities
Translate requirements into clear test strategies, test cases, and acceptance criteria for mobile, web, and backend services.
Design, build, and execute manual and automated test suites (functional, regression, integration, UI/UX, API, and smoke).
Implement and maintain automation frameworks to expand coverage and reduce cycle time across platforms.
Coordinate test planning and execution across teams and releases; ensure environments are ready and deployments are validated.
Identify, document, and track defects through resolution for both test and production environments; prevent regressions with robust coverage.
Assess UI consistency and usability, providing actionable feedback to product and design.
Report quality metrics and risks (coverage, pass/fail rates, defect trends) and communicate status to stakeholders.
Continuously improve QA processes, tooling, and standards; contribute to Agile ceremonies and release readiness.
Key Requirements
5+ years in Quality Engineering/QA, including retail or consumer-facing environments; BS/MS in Computer Science, Engineering, Information Systems, or related field.
Hands-on test automation with tools such as Selenium, Cypress, Appium; strong experience authoring maintainable test suites and frameworks.
Strong understanding of retail operations and workflows (e.g., POS, store/mobile devices, inventory/price/promo, order fulfillment).
Experience testing globally deployed applications (multi-region, multi-language), including data, configuration, and localization nuances.
Solid Agile experience (sprint planning, stand-ups, retrospectives); comfortable working in fast-paced, cross-functional teams.
CI/CD and cloud familiarity-exposure to pipelines and cloud-native testing (AWS preferred).
Analytical problem-solver with proven ability to isolate issues across layers (client, API, data, environment) and drive to resolution.
Excellent communication and collaboration skills; able to articulate quality risks and influence outcomes with stakeholders.
Nice to Have
Ownership across the full application lifecycle (planning through post-release support).
Experience with performance testing, monitoring/observability, and test data management.
Knowledge of DevOps practices for mobile and web platforms.
$66k-89k yearly est. 1d ago
Manufacturing Equipment Quality Technician
Mastech Digital 4.7
Newton, MA jobs
The Equipment Qualification Technician is responsible for verifying, qualifying, and maintaining the quality and performance of manufacturing equipment (not finished products). This role focuses on ensuring machines and production systems operate reliably, meet qualification standards, and comply with regulatory requirements in a manufacturing environment.
Key Responsibilities:
Perform IQ, OQ, and PQ on manufacturing equipment
Verify machine performance, functionality, and compliance (not product inspection)
Document qualification results, deviations, and corrective actions
Work hands-on on the manufacturing floor / shop environment
Support equipment setup, troubleshooting, and issue resolution
Work around production lines, machines, and industrial systems
Partner with Engineering, Quality, and Operations teams
Participate in root cause analysis, audits, and process improvement activities
Train operators and provide technical support once equipment is qualified
Experience
Prior experience in a manufacturing environment (required)
Experience working with machines, equipment, or production lines
Experience in regulated environments (GMP / ISO preferred)
Technical Skills
Equipment qualification or validation exposure (IQ/OQ/PQ preferred)
Mechanical aptitude with hands-on troubleshooting and equipment setup
Ability to follow and document technical procedures
$40k-53k yearly est. 3d ago
Quality Technician
Mastech Digital 4.7
Newton, NC jobs
Key Responsibilities:
Equipment Qualification:
• Perform Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols for new and existing equipment.
• Ensure equipment meets regulatory standards (e.g., FDA, ISO, GMP, etc.) and internal quality requirements.
• Document and report qualification results, including deviations and corrective actions.
• Hands on activities to troubleshoot and resolve technical issues with newly installed equipment.
• Brainstorming with subject matter experts (SME) to do Root Cause Analysis (RCA).
• Utilize standard process improvement methodologies such as FMEA, Six Sigma, DOE, Hypothesis Tree, DMAIC, Fishbone Diagram.
• Work with trained operators to learn how to setup equipment and be trainer to train others.
Testing and Calibration:
• Conduct regular equipment testing and calibration to ensure proper functioning.
• Troubleshoot and resolve issues with equipment performance.
• Documentation and Reporting:
• Prepare detailed reports documenting qualification processes, outcomes, and compliance.
• Maintain accurate and up-to-date records of all equipment qualifications and calibrations.
• Compliance and Regulatory Standards:
• Ensure adherence to regulatory and industry standards such as Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), ISO standards, or other applicable guidelines.
• Assist in audits and inspections as needed.
• Equipment Maintenance and Support:
• Collaborate with engineering, maintenance, and quality teams to ensure proper equipment care and operation.
• Provide training and technical support to staff using qualified equipment.
Continuous Improvement:
• Identify opportunities to improve equipment qualification processes and implement best practices.
• Stay updated on changes to regulatory standards and industry advancements.
Qualifications:
Education:
• Associate's or bachelor's degree in engineering, science, or a related technical field. Relevant certifications may be considered.
Experience:
• 1-3 years of experience in equipment qualification or a related role.
Technical Skills:
• Knowledge of equipment qualification protocols (IQ, OQ, PQ).
• Familiarity with regulatory requirements (e.g., ISO, OSHA)
• Proficiency with diagnostic tools and calibration equipment.
• Industrial equipment operation and troubleshooting.
$31k-41k yearly est. 3d ago
Quality Lead 1st Shift
Advance Services 4.3
Houston, TX jobs
Quality Lead - Entry Level 1st Shift Advance Services inc. is hiring Quality Lead for the northwest Houston "climate controlled" plant. This role involves working closely with Quality Management to help oversee the production floor, ensuring quality standards are met consistently, attention to detail is required as well as standing for up to 10 hours a day
Shift is Monday to Friday and sometimes sat and sun. Weekends are required if scheduled with some overtime and weekend work as required unless otherwise previously approved to be off of work.
Pay $14.00 per hour
Key Responsibilities:
Support quality assurance processes on the production floor
Collaborate with leadership to maintain high standards of production
Identify and help resolve quality-related issues
Maintain accurate records and reports using basic computer tools
Promote a culture of professionalism, respect, and integrity
Basic Requirements:
Leadership experience (preferred but not mandatory)
Strong commitment and reliability
Attention to detail
Basic computer skills
Respectful and professional demeanor
Honesty and integrity
Problem-solving abilities
Ability to work flexible hours, including weekends and extended shifts (10-12 hours as needed)
English proficiency
Why work for Advance Services, Inc.
We are your employment specialists
Never a fee
Weekly pay
Safety and attendance incentives
Health Benefits
PTO
Referral Incentives
Apply for this job by clicking the apply button, applying our website and selecting a branch near you or calling our office at**************
Please complete online application and Stop in and see our experienced friendly staff at 1530 W Sam Houston Pkwy, Houston, Tx 77043 to be considered for this immediate opportunity.
Advance Services is an equal opportunity employer.
$14 hourly 3d ago
Quality Control Associate - 2nd shift
Adecco 4.3
Hartford, CT jobs
Adecco is assisting a local customer who is currently seeking a Quality Control Associate to perform inspections including receiving materials and dimensional/positional accuracy of parts. Candidate must have a basic understanding of QC policies, methods and procedures. The hours for this position are 2:30 p.m. - 11:00 p.m. Training for this position will be required on the day shift. The rate of pay is $27.66 per hour. If your skill meet the requirements below, apply now to Adecco.com.
Responsibilities include but are not limited to:
· Inspects and reports on manufacturing/material quality
· Inspect incoming materials, packaging and labeling components, work-in-process and final products using basic inspection gauging
· Initiate rejection reports for non-conforming materials
· Ensuring proper completion of required documentation in accordance with departmental, GMP, and ISO requirements
· Performs activities in Quality Control department such as incoming, CQA and final product inspections
· Drive process changes, report on quality metrics and ensure proactive measures are taken to achieve quality goals
· Document quality issues and performance measures for management review
· Document corrective actions and track subsequent follow-up activities
· Prepare and present quality status and performance improvements
· Initiate rejection reports for non-conforming materials
· Identify and champion resolution of quality issues
Requirements:
High School diploma or equivalent degree
Minimum of two years' experience with inspecting mechanical parts and assemblies.
Apply Now for consideration for this QC position! Adecco.com
The Adecco benefits offerings include medical, vision, dental, life insurance, short term disability, additional voluntary benefits, EAP program, commuter benefits, and a 401k plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick leave, where required by law, any other paid leave required by Federal, State or local law, and Holiday pay upon meeting eligibility.
Pay Details: $27.66 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
The California Fair Chance Act
Los Angeles City Fair Chance Ordinance
Los Angeles County Fair Chance Ordinance for Employers
San Francisco Fair Chance Ordinance
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
$27.7 hourly 1d ago
QA/Tester with Routers
Business Integra 3.6
Tampa, FL jobs
Duration: 1 year
QA/Tester who can log into and verify Routers . Experience in Automation, Java, SOAP UI, XML, Workflow, Routers, Switches, Telecom experience.
Additional Information
All your information will be kept confidential according to EEO guidelines.
$57k-74k yearly est. 1d ago
QA/Tester with Routers
Business Integra 3.6
Tampa, FL jobs
Duration: 1 year
QA/Tester who can log into and verify Routers . Experience in Automation, Java, SOAP UI, XML, Workflow, Routers, Switches, Telecom experience.
Additional Information
All your information will be kept confidential according to EEO guidelines.
Logical Paradigm is a professional staffing and solutions firm providing flexible and permanent staffing solutions in the skill areas of; Information Technology, Government, Insurance and Financial Services, Healthcare, Pharmaceutical and Clinical Research. Within our staffing offering, we provide temporary, temporary-to-hire, direct placement services for individual as well as full team placements.
Job Description
We are looking for a QA Analyst to assess software quality through manual testing. You will be responsible for locating and reporting bugs and glitches.
In this role, you should have an eye for detail in addition to excellent communication skills. If you are recent STEM graduate with strong analytical mindset and are passionate about quality, we'd like to meet you.
Job Responsibilities include:
Follow established QA processes for manual testing and automation testing
Develop expertise in applications/modules assigned for testing
Work with Agile Team Members to create Test Plans for assigned projects
Work with Agile Team Members to successfully complete Sprints and produce on-time releases
Determining time estimates and testing priorities
Documenting and reporting issues
Tracking issue resolution
Additional Information
BENEFITS:
- Competitive Salary Package with Benefits and periodic reviews (usually every 3 months) and increments.
- Health and Dental Insurance
- Skills Enhancement Data Analytics Training Program is provided for selected candidates.
For more information, please contact ************
$69k-96k yearly est. 1d ago
QA Associate
Artech Information System 4.8
Morris Plains, NJ jobs
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
The incumbent will have responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements.
Coordinates and performs batch record issuance for internally manufactured products Reviews and approves manufacturing and QC related documents for raw material disposition.
Reviews and approves manufacturing and QC related documents for manufactured media Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center Support cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance.
Control costs within department to meet budget.
Complete job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements.
Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed.
Skills:0-3 years GMP manufacturing and/or QA related experience
Education: BS/BA in Biological Sciences or equivalent relevant career experience
Qualifications
Skills:
0-3 years GMP manufacturing and/or QA related experience
Education: BS/BA in Biological Sciences or equivalent relevant career experience
Additional Information
Sneha Shrivastava
Technical Recruiter (Clinical/Scientific)
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: ************ | Fax: ************
Connect with us on - LinkedIn | Facebook | Twitter
$53k-71k yearly est. 1d ago
QA Associate
Artech Information System 4.8
Morris Plains, NJ jobs
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
1. The incumbent will have responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements.
2. Coordinates and performs batch record issuance for internally manufactured products Reviews and approves manufacturing and QC related documents for raw material disposition.
3. Reviews and approves manufacturing and QC related documents for manufactured media Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center Support cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance.
4. Control costs within department to meet budget. Complete job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements.
5. Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed. Skills:0-3 years GMP manufacturing and/or QA related experience
6. Education: BS/BA in Biological Sciences or equivalent relevant career experience
Additional Information
Regards,
Anuj Mehta
************
$53k-71k yearly est. 1d ago
QA Associate
Artech Information System 4.8
Morris Plains, NJ jobs
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
1. The incumbent will have responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements.
2. Coordinates and performs batch record issuance for internally manufactured products Reviews and approves manufacturing and QC related documents for raw material disposition.
3. Reviews and approves manufacturing and QC related documents for manufactured media Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center Support cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance.
4. Control costs within department to meet budget. Complete job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements.
5. Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed. Skills:0-3 years GMP manufacturing and/or QA related experience
6. Education: BS/BA in Biological Sciences or equivalent relevant career experience
Additional Information
Regards,
Anuj Mehta
************
$53k-71k yearly est. 60d+ ago
Quality Assurance Associate
Pharmaron 4.5
Woburn, MA jobs
Quality AssuranceAssociate Salary: $65,000 to $75,000 per year FLSA Classification: Exempt Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit ******************
Job Overview:
The Quality AssuranceAssociate will work in a GxP compliant Bioanalytical CRO Laboratory and will be responsible for daily QA duties under the supervision of the Lead Quality Specialist. This onsite role will support the development, implementation, and maintenance of the Pharmaron (Boston) Lab Services Quality Management System.
Responsibilities:
* Perform administrative and support tasks to assist PLSB Head of Quality in maintaining all key Quality Systems including but not limited to; Document Control, Training and Qualification Management, Deviation and CAPA Management, Audits and Inspections, Equipment Qualification and Management, Archival and Records Management, and tracking and trending.
* Perform initial intake, documentation, notification, administrative review, tracking, filing, and completion support for records related to the above referenced quality systems.
* Ensure all records are indexed, labeled, tracked, and filed appropriately in paper and electronic format.
* Maintain robust cross-referencing tracking tools with required information to support Head of Quality review of trends, risks, issues, and gaps.
* Provide reports to Lead Quality Specialist of upcoming, outstanding, and incomplete tasks and events.
* Support PLSB technical and laboratory staff in navigating basic QA procedures and escalate issues to Head of Quality when appropriate.
* Assist Head of Quality on all assigned projects, including reconciliation and organization of legacy information for increased accuracy, reduced error, closure of historical gaps, and ease of access.
* Additional duties, as required
What We're Looking For:
We're seeking individuals who have strong communication skills with attention to detail who thrive in fast-paced environments.
* Bachelor's degree in science, preferably in biology or similar field (preferred)
* Two years of Quality Assurance experience within the pharmaceutical or biotechnology industry, in a regulated environment; GLP or other regulatory experience is desired
* ISO 9001:2015 Quality Systems experience, a plus
* Strong technical writing skills
Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centred" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
* Insurance including Medical, Dental & Vision with significant employer contributions
* Employer-funded Health Reimbursement Account
* Healthcare & Dependent Care Flexible Spending Accounts
* 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance
* 401k plan with generous employer match
* Access to an Employee Assistance Program
How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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