Quality Assurance Associate jobs at Pwc - 1598 jobs
Managed Services - Salesforce Test Lead - Senior Associate
PwC 4.8
Quality assurance associate job at Pwc
Industry/Sector Not Applicable Specialism Managed Services Management Level Senior Associate At PwC, our people in software and product innovation focus on developing cutting-edge software solutions and driving product innovation to meet the evolving needs of clients. These individuals combine technical experience with creative thinking to deliver innovative software products and solutions.
In testing and quality assurance at PwC, you will focus on the process of evaluating a system or software application to identify any defects, errors, or gaps in its functionality. Working in this area, you will execute various test cases and scenarios to validate that the system meets the specified requirements and performs as expected.
Focused on relationships, you are building meaningful client connections, and learning how to manage and inspire others. Navigating increasingly complex situations, you are growing your personal brand, deepening technical expertise and awareness of your strengths. You are expected to anticipate the needs of your teams and clients, and to deliver quality. Embracing increased ambiguity, you are comfortable when the path forward isn't clear, you ask questions, and you use these moments as opportunities to grow.
Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to:
* Respond effectively to the diverse perspectives, needs, and feelings of others.
* Use a broad range of tools, methodologies and techniques to generate new ideas and solve problems.
* Use critical thinking to break down complex concepts.
* Understand the broader objectives of your project or role and how your work fits into the overall strategy.
* Develop a deeper understanding of the business context and how it is changing.
* Use reflection to develop self awareness, enhance strengths and address development areas.
* Interpret data to inform insights and recommendations.
* Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements.
The Opportunity
As part of the Software and Product Innovation - Testing and Quality Assurance team you are responsible for the creation and implementation of impactful testing methodologies and quality assurance processes. As a Senior Associate you analyze complex problems, mentor others, and maintain rigorous standards. You focus on building client relationships, managing test delivery engagements, and developing a deeper understanding of the business context.
Responsibilities
* Lead the development and execution of reliable testing methodologies
* Oversee the implementation of quality assurance processes
* Analyze intricate issues to provide solutions
* Mentor and guide junior team members
* Maintain excellence in deliverables
* Build and nurture client relationships
* Manage test delivery engagements effectively
* Develop a thorough understanding of the business context
What You Must Have
* High School Diploma
* 3 years of experience
What Sets You Apart
* Bachelor's Degree in Computer Engineering preferred
* Project Management Professional (PMP), or Agile Certification preferred
* Evaluating and appraising the lifecycle of a defined Testing Methodology
* Managing Test Delivery engagements
* Utilizing leading practice application and integration testing
* Providing testing recommendations and organizational designs
* Managing technical teams and engagements
* Assessing end-to-end integrated systems
* Conducting quantitative and qualitative analyses of large and complex data
Travel Requirements
Up to 60%
Job Posting End Date
Learn more about how we work: **************************
PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: ***********************************
As PwC is an equal opportunity employer, all qualified applicants will receive consideration for employment at PwC without regard to race; color; religion; national origin; sex (including pregnancy, sexual orientation, and gender identity); age; disability; genetic information (including family medical history); veteran, marital, or citizenship status; or, any other status protected by law.
For only those qualified applicants that are impacted by the Los Angeles County Fair Chance Ordinance for Employers, the Los Angeles' Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, San Diego County Fair Chance Ordinance, and the California Fair Chance Act, where applicable, arrest or conviction records will be considered for Employment in accordance with these laws. At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship to responsibilities such as accessing sensitive company or customer information, handling proprietary assets, or collaborating closely with team members. We evaluate these factors thoughtfully to establish a secure and trusted workplace for all.
Applications will be accepted until the position is filled or the posting is removed, unless otherwise set forth on the following webpage. Please visit this link for information about anticipated application deadlines: ***************************************
The salary range for this position is: $77,000 - $202,000. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. All hired individuals are eligible for an annual discretionary bonus. PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation, personal and family sick leave, and more. To view our benefits at a glance, please visit the following link: ***********************************
$77k-202k yearly Auto-Apply 39d ago
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Oracle PeopleSoft QA Lead - Financials Delivery Expert
Accenture 4.7
San Francisco, CA jobs
A global professional services company is hiring for a local project-based role with Accenture Flex in San Francisco, California. The role requires expert proficiency in Oracle PeopleSoft Financials and Account Delivery Management. Candidates must have a HS Diploma or GED. The compensation ranges from $45 to $55 per hour, with access to competitive rewards and benefits programs. The position allows employees to work primarily on-site in their local metro area.
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$45-55 hourly 5d ago
Quality Assurance
Eclipse Advantage 3.6
Swedesboro, NJ jobs
Kickstart a Rewarding Career in the Supply Chain Industry with Eclipse Advantage! About Us: At Eclipse Advantage, our values drive everything we do: Win as One, Be Customer Obsessed, Empower with Purpose, Raise the Bar, and Do Right Relentlessly. These aren't just words, they're how we show up every day. If you're someone who loves working as part of a team, takes pride in delivering great results, wants the ability to own your work, and is always looking for ways to grow while doing the right thing, then Eclipse Advantage is the place for you.
Job Description:
The Quality Assurance responsibilities include ensuring product quality and safety through routine testing and monitoring procedures. Candidates should have at least two years of work experience; prior QA experience is desired, with food industry experience preferred but not required. Responsibilities include product testing such as temperature checks and random quality checks. The position requires availability to work one weekend day. Training will be provided.
Don't wait! Call or text "Swedesboro" to ************ to speak with an Eclipse Advantage representative and begin the onboarding process!
Pay Range: $19.50 - $19.50 per hour
Shift:
First Shift: 4:00 AM - start varies, days vary
Second Shift: 2:00 PM - start varies, days vary
Essential Duties and Responsibilities:
-Conduct routine product testing, including temperature checks and random quality inspections
-Monitor and document quality and safety standards
-Identify and report quality issues or deviations
-Follow established QA procedures and protocols
-Maintain accurate and timely records of inspections and test
-Work collaboratively with production staff to ensure compliance
-Participate in training and apply learned quality assurance practices
-Perform duties as assigned, including working one weekend day
Job Requirements:
-Minimum of two years of work experience
-Quality Assurance experience preferred; food industry experience a plus but not required
-Ability to work one weekend day as scheduled
-Strong attention to detail and ability to follow procedures
-Willingness to learn; training will be provided
-Ability to stand for extended periods and work in a production environment
Benefits:
-Health, Dental, and Vision Insurance: Comprehensive coverage for employees and their families
-Retirement Plans: A 401k with employer matching
-Voluntary benefits: Life, accident, and disability products available for employee and dependents
Bonus Eligibility:
Referral Bonus: Earn $50 for every successful referral after they complete 80 hours of work.
-No limit on the number of referrals.
-Managers confirm referrals during interviews to ensure bonus eligibility.
Eclipse Advantage is an Equal Opportunity Employer, and qualified applicants will receive consideration for employment without regard to race, religious creed, color, national origin, ancestry, physical disability, mental disability, reproductive health decision-making, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, age, sexual orientation, veteran or military status, or any other characteristic protected by applicable law.
Bring your experience and take the next step in your career. We're looking for skilled professionals ready to make an impact. Apply today!
PandoLogic. Keywords: Quality Control / Quality Assurance Specialist, Location: Swedesboro, NJ - 08085
$19.5-19.5 hourly 2d ago
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
Quality Assurance Associate
Yoh, A Day & Zimmermann Company 4.7
Maryland Heights, MO jobs
Yoh is hiring a Quality AssuranceAssociate for our Pharmaceutical Manufacturing client in St. Louis, Missouri. This is a great opportunity to expand your skillsets and join a growing team! Schedule: 8:00 am - 4:30 pm, Monday - Friday Job Responsibilities:
Ensure completion of require training, work (including document review, batch release, QA on-the-floor, AQLs), and timely release of materials and batches.
Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP).
Responsible for the thorough and efficient review and disposition of completed batch record documentation ensuring adherence to Good Documentation Practices, cGMPs and applicable local procedures.
Responsible for performing and / or overseeing performance of Quality Assurance On The Floor tasks including but not limited to performing AQL inspections, performing clearances for manufacturing areas and providing Quality input and guidance to manufacturing personnel.
Responsible for with dispositioning finished product, raw materials/ components and intermediates through an all-inclusive documentation review and cross reference of electronic quality systems.
Responsible with release of incoming raw materials and components per applicable local procedures. This may include support for labeling dispositioned raw materials and components with appropriate status indicator labels.
Ensure a safe and quality working environment through training, awareness, and compliance to safety/Quality guidelines and SOP's.
Ensure the maintenance of department, premises and equipment.
Perform all work in compliance with site safety and radiation protection guidelines.
Assist with quality investigations in order to determine root cause and applicable CAPAs.
Skills/Education Required:
Associate Degree in life science
Bachelor Degree in life science or a related field preferred.
Work experience is considered in lieu of degree.
Three or more years of quality and production experience in a cGMP environment/facility.
#IND-SPG
Estimated Min Rate: $27.00
Estimated Max Rate: $29.00
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: **********************************
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.
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$70k-93k yearly est. 4d 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.
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$70k-93k yearly est. 4d ago
SAP S/4HANA QA Specialist II
The Fountain Group 4.6
Illinois jobs
HYBRID North Chicago IL Pay:$31-$34/hr Hybrid Onsite Schedule: 3 days on site, 2 days remote REQUIRED:
SAP S4/Hana experience
Quality Management systems experience including Document management system
Minimum Bachelor's degree, background in software engineering or software quality assurance, Engineering or other technical/ scientific area or equivalent experience.
RESPONSIBILITIES:
Maintenance, Configuration and Implementation of data for Client's Market Authorization control system.
Knowledge or experience in requirements gathering, analysis techniques, software verification/validation techniques, configuration management techniques or documentation standards.
SAP S4/HANA and TrackWise experience preferred.
Good verbal and written communication skills. Knowledge or experience in computerize system validation/testing;
The candidate is responsible for all software quality assurance activities such as evaluation of software lifecycle (SLC) deliverables for compliance with Operating Procedures, FDA requirements and the CFR including 21 CFR Part 11.
Lead or participate in various reviews, risk analyses and other software quality assurance activities with primary focus on review and approval of restrictions, configurations, and validation supporting documents.
Have a background in software engineering, software lifecycle activities, or software validation and be familiar with the work products that result from SLC key activities.
The candidate should be familiar with IEEE, SEI, ISO and have experience in a regulated environment. Analytical and troubleshooting skills are important, as is the ability to manage tasks. Must be able to manage multiple tasks and resources.
Support project teams in planning, preparation, reviewing and approval of quality documents. Create quality system documentation with guidance from technical teams following approved templates and guidelines.
Collect and compile key quality metric data.
Assist with processing configuration and restriction implementation within SAP S4/ HANA enterprise system.
Ability to maintain a high degree of accuracy and analytical thinking.
Works well with manager guidance to complete tactical objectives while able to manage own time effectively.
Perform assessments to determine compliance to processes and regulations to identify potential gaps and suggest improvements within our quality system.
Assist in the design of effective quality systems, procedures and/or processes to ensure compliance as well as efficiency throughout our quality system.
Daily job responsibilities they vary but overall: Primary focus on creating, review and approval of project deliverables, and compliance with applicable Operating Procedures, FDA requirements and the CFR including 21 CFR Part 11. Responsible for complying with international regulatory requirements. Also, participate in various software lifecycle (SLC) deliverables reviews, risk analyses, troubleshooting business related issues and other quality assurance activities.
Are you open to look at candidates willing to relocate? Prefer local
What are the top 3-5 skills requirements should this person have?:
Experience working with software lifecycle deliverables and ability to incorporate updates
to meet the needs of the business and project teams;
Effective time management and ability to adjust workload to meet customer needs;
Good interpersonal skills with the ability to work collaboratively with multiple project teams of differing backgrounds
Must be able to work 50 weeks out of the year, excluding Client holidays.
What is a nice to have (but not required) regarding skills, requirements, experience, education, or certification?
Quality Management System - Change Management module, and technical skills - implementation and configuration are preferred; Understanding of computerize system Testing.
Hands-on professional with experience in the software lifecycle (SLC).
What type of environment is this person working in? Individual contributor able to work
independently as well as within a team
Work Schedule (Define days, # of hours)/ Is Overtime offered or required? If yes, how many hours,
what impact to scheduled working hours? Monday - Friday, 8 hours days; 40 hours a week. Start
time: 8:00 AM CST. Overtime - limited but requires manager approval.
Does this position offer the ability to work remotely on a regular basis or is it an on-site role? If remote opportunity exists, what are the options (i.e. 1 day remote, 4 days on-site)?
3 days on site (Tue, Wed, Thur) and 2 days remote (If needed, Mon and Friday onsite work is possible).
Is the worker onshore or offshore? Onshore
Will there be Domestic and/or International Travel? No Travel
$31-34 hourly 2d 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
Wound Care 4.2
Upland, CA jobs
!!! NOW HIRING !!! - Quality Assurance (QA) | Wound Care
We are seeking an experienced Quality Assurance (QA) professional with extensive wound care expertise to oversee clinical documentation quality, provider visit management, and compliance for a growing wound care organization.
This role is critical to ensuring accurate provider documentation, Medicare compliance, and timely billing.
Role Overview
As a QA - Wound Care, you will be responsible for reviewing and validating provider documentation, coordinating provider visits, and ensuring all wound care services are documented correctly, compliantly, and billed accurately.
Key Responsibilities
Perform QA review of all provider clinical notes for accuracy, completeness, and compliance
Ensure provider documentation meets Medicare wound care guidelines
Manage and track provider visits to ensure timely completion of notes
Communicate directly with providers to correct, clarify, and complete documentation
Collaborate closely with billing and revenue cycle teams to ensure visits are billed appropriately
Assist and educate wound care providers on proper documentation standards and compliance requirements
Review and validate ICD-10 diagnosis codes related to wound care services
Ensure documentation accuracy within EMR systems
Identify documentation trends and opportunities for provider education and process improvement
Required Qualifications
Extensive experience in wound care (clinical or QA/compliance role)
Proven experience performing QA review of provider notes
Strong knowledge of Medicare guidelines related to wound care services
Experience managing and coordinating provider visits and documentation timelines
Familiarity with EMR systems
Strong working knowledge of ICD-10 coding for wound care-related services
Ability to communicate effectively with providers, clinical teams, and billing staff
High attention to detail and strong organizational skills
Preferred Qualifications
RN, LVN, NP
Prior experience in mobile wound care, home health, or outpatient wound clinics
Experience working directly with billing, coding, or revenue cycle teams
Why Join Us
Key leadership support role impacting compliance and revenue integrity
Collaborative clinical and billing teams
Opportunity to educate and shape provider documentation standards
Stable and growing wound care organization
Compensation & Benefits
Salary Range: $80,000 - $100,000 annually (based on experience and workload)
Comprehensive benefits package, including but not limited to:
Health, Dental, Vision Insurance
401(k)
Paid Time Off (PTO)
Performance Bonuses
How to Apply
Apply directly on LinkedIn.
Qualified candidates may be asked to provide examples of QA or documentation review experience.
$80k-100k yearly 4d ago
Quality Assurance Coordinator - Corporate Housing
Alchemy Global Talent Solutions 3.6
Tampa, FL jobs
Join the thriving corporate housing industry as a Quality Assurance Coordinator based remotely in the United States. This exciting opportunity involves working in a fast-paced environment where attention to detail and quality service are key.
If you're organised, proactive, and ready to ensure top-tier guest experiences, this role is for you.
What You'll Be Doing:
Conduct quality inspections to verify properties meet defined standards.
Maintain detailed inspection records using computerised systems.
Coordinate with internal departments and vendors to resolve quality concerns.
Monitor and uphold service quality for temporary housing accommodations.
Manage scheduling and tracking of inspections to maximise efficiency.
Prepare reports and summaries of inspection findings.
Support day-to-day operations and assist with administrative duties.
Implement and follow up on corrective actions for any identified issues.
Communicate quality expectations clearly to service providers.
Participate in process improvement initiatives related to guest accommodations.
Ensure documentation and filing systems are kept up to date.
Deliver exceptional customer service in all interactions.
What We're Looking For:
Previous experience in the moving, relocation, or corporate housing industry.
Strong organisational skills with keen attention to detail.
Proven ability to work independently and within a team.
Proficiency in Microsoft Office Suite and other relevant software.
Excellent verbal and written communication skills.
Effective time management and task prioritisation.
$43k-64k yearly est. 3d ago
Quality Assurance Specialist
TRS Staffing Solutions 4.4
Charleston, SC jobs
Quality Assurance Specialist
Shifts available:
2nd Shift | Monday - Friday | 3:00 PM - 11:00 PM
3rd Shift | Sunday - Thursday |11:00PM - 7:30PM
(off-shifts receive a shift premium bonus)
Compensation: $65,000 - $85,000
Benefits: Full Benefits Package | Paid Time Off | 401(k) | Relocation Assistance Available
Overview:
We are seeking a detail-oriented and experienced Quality Assurance Specialist to join our team in a sterile manufacturing environment. This role is critical to ensuring compliance with cGMP standards and maintaining the highest levels of product quality and data integrity. The ideal candidate will have hands-on experience in sterile manufacturing, environmental monitoring, and quality documentation processes.
Key Responsibilities
Perform quality review and approval of deviations, investigations, batch records, protocols, and reports.
Conduct floor audits and inspections to ensure compliance with GDP and data integrity standards.
Support client and regulatory audits, providing documentation and insight as needed.
Oversee the release of support materials, products, equipment, and facilities.
Maintain and analyze quality databases; identify trends and improvement opportunities.
Develop and revise SOPs and other quality documentation.
Provide training and consultation on quality and compliance topics.
Ensure timely and accurate completion of all cGMP and company training requirements.
Actively contribute to the site's Quality Management Systems (QMS), including investigations, CAPAs, and change controls.
Qualifications
Bachelor's degree in Chemistry, Biology, or a related field with 3+ years of relevant experience, or a Master's degree with 1+ year of experience Required
Demonstrated experience in GMP-regulated environments.
Preferred experience in environmental monitoring and critical utilities within sterile operations.
Strong understanding of GDP, data integrity, and quality assurance processes in manufacturing
Must be authorized to work in the US without sponsorship
Skills & Competencies
Proficient in Microsoft Office and CRM tools (e.g., Salesforce, HubSpot).
Excellent written and verbal communication skills.
Strong analytical and problem-solving abilities.
Ability to work independently and collaboratively across teams.
Comfortable interacting with clients, regulatory agencies, and internal stakeholders.
Ability to mentor and train others on quality and compliance topics.
Work Environment & Physical Demands
This is a 100% on-site role.
May require standing, walking, sitting, and lifting up to 50 lbs.
Occasional exposure to mechanical parts, elevated workspaces, and vibration.
Must wear appropriate PPE, including safety eyewear, respirators, lab coats, and gloves.
Noise levels may vary depending on the work area (lab, manufacturing, office)
$65k-85k yearly 3d ago
Quality Assurance Specialist III
Us Tech Solutions 4.4
North Chicago, IL jobs
Primarily responsible for supporting the Client Research and Development quality agreement process with a focus on identifying and implementing process improvements.
Lead or participate in technically complex and strategic cross-functional projects, demonstrating the ability to work across various teams.
Drive or support strategic initiatives aimed at improving compliance with regulatory requirements and standards.
Take a proactive role in process improvements, which includes the review and update of current supporting processes and procedures to enhance efficiency and effectiveness.
Achieve a difficult balance of involvement, independence, and objectivity.
Provide support for periodic review of Quality Agreements, ensuring alignment with organizational and regulatory expectations.
Collect, analyze, and report relevant metrics to inform decision-making and track the effectiveness of initiatives.
Consistently demonstrate Client's Ways of Working and Leadership Attributes including a collaborative mindset and leadership. Create a learning environment, embrace the ideas of others, and manage innovation to reality.
Experience/Skills:
Bachelor's degree preferable in a physical science, life science, pharmacy, business, engineering or equivalent experience required
5-7 years of experience in Quality Assurance / Regulatory Affairs (Pharmaceutical or Medical Device preferred)
3-5 years of experience in clinical research and development or manufacturing, or analysis of investigational products
Minimum of 7 years' total combined experience required (Not necessarily the sum of the above)
Must have experience with quality agreements and knowledge of worldwide regulatory requirements that influence their content.
Persuasive, effective communication skills are essential with an ability to work effectively across functions, across technical areas, and outside of the company.
Must have excellent oral/written communications skills, interpersonal skills, leadership, tact, open mindedness, maturity, tenacity, decisiveness, self-reliance, organizational / administrative skills, and sound judgment.
Assures the quality of manufactured products and processes per standard operating processes(SOP'S) and GMP (Good Manufacturing Practices). BS degree and/or 7 to 7 years equivalent experience
Responsibilities:
Provide an active role within R&D as an expert in GCP requirements. The strategic focus is for early detection and prevention, followed by correction of issues.
Collaborate with GCP functional areas and assist in the resolution of external partner quality issues.
Lead or participate in technically complex and strategic cross functional GCP projects.
Lead or participate in GCP focused strategic initiatives to improve compliance with regulatory requirements and standards.
Lead or participate in process improvements, including review / update current supporting processes and procedures
Achieve a difficult balance of involvement, independence, and objectivity.
May support Clinical Quality Agreement creation and periodic review.
Consistently demonstrate Client's Ways of Working and Leadership Attributes including a collaborative mindset and leadership. Create a learning environment, embrace the ideas of others, and manage innovation to reality.
Qualifications:
Bachelor's Degree preferably in technical or scientific area (Chemistry, Pharmacy, Biology, Microbiology, or Engineering) or equivalent industry experience (at least 8 years) with sufficient exposure to pharmaceutical, medical device, or combination product related industries.
Thorough understanding of international GCP regulatory standards.
Must have a technical background and extensive knowledge of worldwide requirements for quality systems.
Must have excellent oral/written communications skills, interpersonal skills, leadership, tact, open mindedness, maturity, tenacity, decisiveness, self-reliance, organizational / administrative skills and sound judgment.
Persuasive, effective communication skills are essential with an ability to work effectively across GCP functions, across technical areas and outside of the company.
Accreditation by a professional body is desirable, e.g., American Society for Quality (ASQ) Certified Quality Manager (CQM), Registered Quality Assurance Professional (RQAP), and/or Certified Quality Auditor (CQA).
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions 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.
Recruiter Details:
Name: Vijay
Email: ******************************
Internal Id: 26-00617
$45k-80k yearly est. 5d ago
Quality Assurance Specialist
Us Tech Solutions 4.4
Fort Washington, PA jobs
Shop Floor QA Specialist
QA Shop Floor - 3rd shift
Must be able to work four 10 hour days
Sun to Wed 9:30pmEST to 8:00AMEST
or
Wed to Sat: 9:30pmEST to 8:00AMEST
The position is responsible for providing daily Quality Assurance support to the manufacturing site to ensure internal and regulatory cGMP and CFR requirements are met. Quality Assurance support areas include but are not limited to Batch Record Review, Product Release, Standard Operating Procedures, Investigations, CAPA, Change Control, Shop Floor Audits. The position will interact with other departments including Manufacturing, Packaging, Quality Laboratories, Quality Systems, Validation, Engineering, Maintenance and other departments as it relates to site Quality Assurance responsibilities.
Responsibilities: (Define key accountabilities and/or activities.) Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and guidelines, this position:
β’ Ensure quality and compliance in all my actions by:
All employees
o Attend GMP training on the schedule designated for my role and as appropriate for my role.
o Adhere to strict compliance with procedures applicable to my role.
o Exercise the highest level of integrity in the tasks that I perform.
o In a timely and prompt manner, identify, report and seek correction for deviations noted in my workplace.
o Embrace a behavior of employee involvement and commitment to doing the job right the first time.
People Managers
o Ensure employees under your scope of responsibility are trained in required procedures for the execution of their role and maintain current with training requirements during the year.
o Promote an environment of employee involvement in the workplace.
o Seek prompt identification, reporting and correction of deviations in the workplace as noted by employees.
1. Quality Assurance and Compliance Focus
β’ Provides daily βShop Floorβ QA support to warehouse, bulk manufacturing and packaging lines.
β’ Provides leadership support to QA Shop Floor activities including communication of quality events to management.
β’ Performs or supports activities related to Batch Record Review, Raw Material, Bulk, and Finished Product Releases.
β’ Provides support to Investigations and/or Investigation Protocols, responsibilities include conducting, writing, reviewing and approvals.
β’ Performs or supports activities related Line Audits, Line or Area Cleaning Verifications
β’ Participates in design of quality processes and creation/modification/approval of Standard Operating Procedures (SOP's).
β’ Provides support to Consumer Complaint investigations.
β’ Provide QA support to various project teams, as needed.
β’ Actively supports Site metrics, compliance improvement and training initiatives.
2. Customer and Performance Improvement Focus
β’ Provide support to capturing of site metrics and promote improvement opportunities.
β’ Facilitate resolution of issues to improve site metrics.
3. People & Organization Focus
β’ Provides training and direction as needed to new employees
β’ Teams with Department members for process feedback and continuous improvement opportunities
β’ Represents Quality Assurance in positive manner
4. Performs other related duties as required.
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions is an Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: I.Prudvi kumar
Email: *******************************
Internal Id: 25- 47837
$52k-90k yearly est. 5d ago
Quality Assurance Supervisor
Provisions Group 4.4
Nashville, TN jobs
About Our Client
Our client is a food manufacturing company producing shelf-stable, canned products. Quality, food safety, and consistency are critical to their operation, and this role plays a key part in protecting the brand, the consumer, and the production process.
Position Overview
The QA Supervisor is responsible for overseeing daily quality assurance activities within a food manufacturing environment, ensuring all products meet internal quality standards and external regulatory requirements. This role leads QA technicians on the floor, supports production in real time, and ensures compliance with food safety programs including HACCP, GMP, and FSMA, with a strong focus on canned and thermal-processed products.
This is a hands-on role that balances people leadership, documentation, and plant-floor presence.
Key Responsibilities
Team Leadership & Daily Operations
Lead, train, and support QA Technicians across production shifts
Assign and prioritize daily QA coverage to support production schedules
Serve as the primary QA point of contact during assigned shifts
Coach team members on food safety, quality standards, and proper documentation
Quality Assurance & Food Safety
Monitor production processes to ensure compliance with product specifications and food safety requirements
Perform and oversee inspections of raw materials, in-process product, and finished goods
Verify adherence to HACCP plans, GMPs, SSOPs, and preventive controls
Ensure proper monitoring of critical control points, especially for thermal processing and canning operations
Testing, Verification & Documentation
Oversee sampling, testing, and verification activities for product quality and food safety
Review and approve batch records, QA logs, corrective actions, and deviation reports
Ensure accurate, timely documentation to support internal audits, regulatory inspections, and customer requirements
Assist with root cause analysis and corrective/preventive actions
Regulatory & Audit Support
Ensure compliance with FDA, USDA (as applicable), and FSMA requirements
Support third-party audits and customer audits (SQF, BRC, FSSC, or similar)
Maintain audit readiness through proper documentation and plant practices
Continuous Improvement & Cross-Functional Collaboration
Partner with Production, Maintenance, and R&D to resolve quality issues
Identify opportunities to improve processes, reduce defects, and strengthen food safety culture
Participate in new product introductions and process changes from a QA perspective
What We're Looking For
Education
Bachelor's degree in Food Science, Microbiology, Chemistry, or a related field preferred
Equivalent hands-on experience in food manufacturing quality may be considered
Experience
3+ years of experience in food manufacturing quality assurance or quality control
Experience in canned foods, thermal processing, or shelf-stable products strongly preferred
Prior supervisory or lead experience required
Skills & Knowledge
Working knowledge of HACCP, GMP, FSMA, and preventive controls
Understanding of thermal processing, CCP monitoring, and food safety documentation
Strong communication and leadership skills
Comfortable working on the production floor and addressing issues in real time
Proficient with Microsoft Office and QA documentation systems
Preferred Certifications
HACCP Certification
Experience with GFSI-recognized programs such as SQF, BRC, or FSSC 22000
Additional Requirements
Ability to work flexible schedules, including weekends, holidays, or off-shifts as needed
Comfortable working in a fast-paced production environment
Physical & Work Environment
Ability to stand and walk for extended periods on the production floor
Occasional lifting up to 25 lbs
Exposure to varying temperatures, food allergens, and manufacturing equipment
$51k-74k yearly est. 2d ago
Production Quality Associate
Adecco 4.3
Joliet, IL jobs
Adecco is excited to announce immediate openings for Production Quality Associates in Joliet, IL, working with a top local client. This is your opportunity to be part of a dedicated team preparing fresh meal kits for delivery, ensuring customers receive delicious meals on time. The starting pay is $17.50 per hour with overtime opportunities available. Plus, you'll enjoy weekly pay, so you don't have to wait long to receive your hard-earned money!
As part of the job, you will work in a refrigerated environment, assembling and packing meal kits. You'll help prepare fresh ingredients and assist with meal cooking, all while ensuring cooking equipment stays clean and in good working condition. Adecco offers comprehensive benefits including medical, dental, vision, and 401(k) options. And if you refer a friend, you'll be eligible for generous referral bonuses!
Previous food, grocery, or restaurant experience preferred, but not required for this position! Candidates must have the ability to read, write and speak English fluently and have basic computer skills. Candidates must be able to stand for the entire shift, lift up to 50 lbs. and stay flexible, as tasks may vary.
If you're ready to get started, simply click "Apply Now" for immediate consideration.
Please note that you will be exposed to the top 8 food allergens: Eggs, Shellfish, Fish, Tree Nuts, Nuts, Wheat, Soy and Milk.
Pay Details: $17.50 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.
$17.5 hourly 12d ago
Quality Assurance Specialist - UL508A
Educated Solutions Corp 3.9
Menomonee Falls, WI jobs
Our Client, a leader in Building Automation Controls Systems is seeking an experienced Quality Assurance Specialist to add to the team in the 15000 square foot facility of UL508A panel building. The purpose of this position is to assure quality and deliver neat and organized building automation UL508A control panels for installation into the field. This role provides βfinal sayβ panel support to this nationwide company of 200+ employees and provides all panel building duties for clients across the nation. The role requires UL508A experience and a highly detailed demeanor. This role delivers strong base pay and bonus and is located onsite in Menomonee Falls, WI. This is a full time position with a strong benefit program, and requires no travel.
The ultimate key to this role is knowledge of the UL 508A standard, with preference to possess the UL MTR (Manufacturer Technical Representative) certification. Candidates must possess background in industrial control / electric panels as this role must be able to read and comprehend wiring diagrams and use and understand tools such as a digital multi-meter. The incumbent will:
Take responsibility for reviewing industrial control panel electrical wiring drawings, inspecting assembled industrial control panels, and ensuring the highest quality standards for a UL 508A Panel Shop.
Review, comprehend, and inspect control panel electrical wiring drawings to ensure each meets required standards.
Review and inspect light industrial control panels for any build or quality related deviations.
Document all drawing and panel errors to identify additional training or process improvements.
Take ownership of UL 508A program and ensure compliance to the standard and to written procedure.
Communicate with and assist UL representative during routine inspections and any other communications.
Research and validate components for UL compliance.
Assist with production related documentation and processes.
Use various software programs to track projects and log other information.
Qualifications
5+ years experience in the electrical panel build arena
2+ years experience specific to UL508A standards
Knowledge of National Electrical Code (NEC).
Experience in the use of testing equipment such as digital multi-meter and other hand tools.
Strong experience in the interpretation of electrical control panel drawings.
Strong knowledge of arithmetic and algebra.
Proficiency with Microsoft Office products and Google drive.
Must be able to stand for majority of the day.
Must be able to manipulate or move up to 100 lbs. while inspecting panels.
Must have good visual perception and be able to hear and respond quickly to verbal instructions.
Must be able to wear safety glasses and steel toe safety boots while inspecting panels in the warehouse.
Preferred but not required
Bachelors or Associates Degree
UL MTR (Manufacturer Technical Representative) certification
$31k-45k yearly est. 4d ago
Senior Quality Assurance Technician
Aegis Worldwide 4.2
Maryland Heights, MO jobs
Senior Quality Assurance Technician - Pharmaceutical Manufacturing
π Maryland Heights, MO | π 1st Shift (8:00 AM - 4:30 PM)
π² $28-29/hr + OT (1.5x)
A pharmaceutical manufacturing organization is seeking a Senior Quality Assurance Technician to support quality operations within a GMP-regulated environment. This role focuses on batch record review, product and material release, and on-the-floor quality support.
Responsibilities
Review and release batch records, raw materials, intermediates, and finished pharmaceutical products
Ensure compliance with cGMPs and applicable regulatory standards
Provide QA on-the-floor support including AQL inspections and manufacturing line clearances
Partner with manufacturing teams to provide real-time quality guidance
Support quality investigations, root cause analysis, and CAPA activities
Maintain accurate GMP documentation and training compliance
Qualifications
3+ years of Quality Assurance experience in pharmaceutical manufacturing
Hands-on experience with batch record review and product/material release
Strong understanding of cGMP and Good Documentation Practices
Experience supporting QA activities on the manufacturing floor
Strong written and verbal communication skills
Ability to work independently and collaboratively in a regulated environment
Why This Role
First-shift schedule
Hands-on QA involvement supporting manufacturing operations
Stable pharma environment with consistent production
π Apply or message directly to learn more.
$28-29 hourly 1d ago
Quality Control Analyst II
Talentburst, An Inc. 5000 Company 4.0
Norton, MA jobs
Industry: Pharmaceuticals
Title: Quality Control Analyst II
Duration: 11 months contract (+Possibility of extension)
This is an onsite role in Norton, MA, with occasional responsibilities at other Client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
Description:
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.
Key Responsibilities'
Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Support weekend lab operations and maintain training records.
Assist in lab equipment and inventory maintenance, including reagent and sample prep.
Review data timely and qualify as a data reviewer.
Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
Contribute to updating controlled documents (SOPs, work instructions, test methods).
Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH).
Participate in continuous improvement initiatives and cross-functional collaboration.
Support regulatory submissions, inspection readiness, and audits
Qualifications:
B.S. in chemistry, biology, biochemistry, or related field.
4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
Experience in method transfer/implementation; understanding of method lifecycle management preferred.
Strong technical writing, data analysis, problem-solving, and organizational skills.
Excellent communication and teamwork.
Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred
$60k-83k yearly est. 4d ago
Managed Services - Salesforce Test Lead - Senior Associate
PwC 4.8
Quality assurance associate job at Pwc
Industry/Sector Not Applicable Specialism Managed Services Management Level Senior Associate At PwC, our people in software and product innovation focus on developing cutting-edge software solutions and driving product innovation to meet the evolving needs of clients. These individuals combine technical experience with creative thinking to deliver innovative software products and solutions.
In testing and quality assurance at PwC, you will focus on the process of evaluating a system or software application to identify any defects, errors, or gaps in its functionality. Working in this area, you will execute various test cases and scenarios to validate that the system meets the specified requirements and performs as expected.
Focused on relationships, you are building meaningful client connections, and learning how to manage and inspire others. Navigating increasingly complex situations, you are growing your personal brand, deepening technical expertise and awareness of your strengths. You are expected to anticipate the needs of your teams and clients, and to deliver quality. Embracing increased ambiguity, you are comfortable when the path forward isn't clear, you ask questions, and you use these moments as opportunities to grow.
Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to:
* Respond effectively to the diverse perspectives, needs, and feelings of others.
* Use a broad range of tools, methodologies and techniques to generate new ideas and solve problems.
* Use critical thinking to break down complex concepts.
* Understand the broader objectives of your project or role and how your work fits into the overall strategy.
* Develop a deeper understanding of the business context and how it is changing.
* Use reflection to develop self awareness, enhance strengths and address development areas.
* Interpret data to inform insights and recommendations.
* Uphold and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements.
The Opportunity
As part of the Software and Product Innovation - Testing and Quality Assurance team you are responsible for the creation and implementation of impactful testing methodologies and quality assurance processes. As a Senior Associate you analyze complex problems, mentor others, and maintain rigorous standards. You focus on building client relationships, managing test delivery engagements, and developing a deeper understanding of the business context.
Responsibilities
* Lead the development and execution of reliable testing methodologies
* Oversee the implementation of quality assurance processes
* Analyze intricate issues to provide solutions
* Mentor and guide junior team members
* Maintain excellence in deliverables
* Build and nurture client relationships
* Manage test delivery engagements effectively
* Develop a thorough understanding of the business context
What You Must Have
* High School Diploma
* 3 years of experience
What Sets You Apart
* Bachelor's Degree in Computer Engineering preferred
* Project Management Professional (PMP), or Agile Certification preferred
* Evaluating and appraising the lifecycle of a defined Testing Methodology
* Managing Test Delivery engagements
* Utilizing leading practice application and integration testing
* Providing testing recommendations and organizational designs
* Managing technical teams and engagements
* Assessing end-to-end integrated systems
* Conducting quantitative and qualitative analyses of large and complex data
Travel Requirements
Up to 60%
Job Posting End Date
Learn more about how we work: **************************
PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: ***********************************
As PwC is an equal opportunity employer, all qualified applicants will receive consideration for employment at PwC without regard to race; color; religion; national origin; sex (including pregnancy, sexual orientation, and gender identity); age; disability; genetic information (including family medical history); veteran, marital, or citizenship status; or, any other status protected by law.
For only those qualified applicants that are impacted by the Los Angeles County Fair Chance Ordinance for Employers, the Los Angeles' Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, San Diego County Fair Chance Ordinance, and the California Fair Chance Act, where applicable, arrest or conviction records will be considered for Employment in accordance with these laws. At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship to responsibilities such as accessing sensitive company or customer information, handling proprietary assets, or collaborating closely with team members. We evaluate these factors thoughtfully to establish a secure and trusted workplace for all.
Applications will be accepted until the position is filled or the posting is removed, unless otherwise set forth on the following webpage. Please visit this link for information about anticipated application deadlines: ***************************************
The salary range for this position is: $77,000 - $202,000. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. All hired individuals are eligible for an annual discretionary bonus. PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation, personal and family sick leave, and more. To view our benefits at a glance, please visit the following link: ***********************************