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Weekend Qa Jobs in Raleigh, NC (NOW HIRING)

The role will serve as Quality-to-Quality client liaison and sometimes SME for the Quality team reporting cross-QA metrics and status for KBI and clients. The role is client-facing. The role will be ...

Knowledge of quality assurance processes and procedures.. Strong interpersonal skills.. Excellent problem solving, risk analysis and negotiation skills.. Strong training capabilities.. Effective ...

Must be willing to participate in occasional evening and weekend work as needed * Willing to work on-site, at least 4 days a week, at our Raleigh, NC location Senior QA Engineer Position Preferences ...

Sr. Quality Assurance Specialist

Durham, NC ยท On-site

$79K - $109K/yr

The Senior Specialist, Quality Assurance provides Quality Assurance (QA) oversight of AskBio's Vendor Qualification Program for GCLP, GLP, GCP (and GMP vendors, as needed). This key individual ...

Connoisseurs in the field of staff augmentation for IT, we operate on 24 by 7 model with an aim of providing affordable and adept professionals with an assurance of satisfaction for both Consultants ...

Sr. Quality Assurance Specialist

Durham, NC ยท On-site

$79K - $109K/yr

The Senior Specialist, Quality Assurance provides Quality Assurance (QA) oversight of AskBio's Vendor Qualification Program for GCLP, GLP, GCP (and GMP vendors, as needed). This key individual ...

Quality Assurance RN

Smithfield, NC ยท On-site

$30 - $40/hr

Join us as a Quality Assurance RN and make a meaningful impact through clinical excellence! Location: Smithfield Manor Rehabilitation and Healthcare Center Compensation & Benefits: * Salary: $30-$40 ...

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Weekend Qa information

See Raleigh, NC salary details

$36.9K

$114.8K

$174K

How much do weekend qa jobs pay per year?

As of Jun 10, 2026, the average yearly pay for weekend qa in Raleigh, NC is $114,777.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,700.00 and $140,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Weekend Qa position, and why are they important?

To excel as a Weekend QA, you need a solid understanding of software testing principles, keen attention to detail, and experience with bug tracking and test case management. Familiarity with automation tools like Selenium, JIRA, and basic scripting languages, as well as ISTQB certification, are often beneficial. Strong communication, problem-solving abilities, and adaptability help Weekend QAs collaborate effectively across distributed teams and manage shifting priorities. These competencies ensure thorough product testing, quick issue resolution, and help maintain software quality during weekend release cycles.

What are the typical responsibilities and work patterns for a Weekend QA position?

As a Weekend QA, your primary responsibilities include executing test cases, identifying and documenting defects, and collaborating with development teams to ensure product quality during weekend releases or maintenance windows. You may work independently or as part of a smaller weekend shift team, often communicating with colleagues through project management tools and virtual meetings. The role typically requires flexibility in hours, as coverage is needed outside the standard work week, but this can offer a better work-life balance for some professionals. Additionally, Weekend QA work is valuable for those seeking exposure to critical deployments, fast-paced troubleshooting, and unique scenarios not encountered during regular business hours. This experience can help build expertise and open doors to more advanced QA roles in the future.

What is a Weekend QA job?

A Weekend QA (Quality Assurance) job typically involves testing software, applications, or products during weekends to ensure they meet quality standards. Weekend QA professionals work part-time or on a contract basis, performing tasks such as identifying bugs, running test cases, and reporting issues to the development team. This role is common in industries requiring continuous testing, such as software development, gaming, and e-commerce. It helps companies maintain quality without disrupting weekday workflows.

What are the most commonly searched types of Qa jobs in Raleigh, NC? The most popular types of Qa jobs in Raleigh, NC are:
What are popular job titles related to Weekend Qa jobs in Raleigh, NC? For Weekend Qa jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Weekend Qa jobs? Cities near Raleigh, NC with the most Weekend Qa job openings:
Infographic showing various Weekend Qa job openings in Raleigh, NC as of June 2026, with employment types broken down into 72% Full Time, and 28% Contract. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $114,777 per year, or $55.2 per hour.
Principal QA Specialist

Principal QA Specialist

KBI Biopharma, Inc.

Durham, NC โ€ข On-site

Full-time

Posted 26 days ago


Job description

Position Summary:
Individual contributor and special project leader responsible for ensuring compliance with internal quality documents, regulatory requirements, and cGMP. The role will serve as Quality-to-Quality client liaison and sometimes SME for the Quality team reporting cross-QA metrics and status for KBI and clients. The role is client-facing.
The role will be responsible for supporting processes required for product release, including deviation investigation guidance and CAPA review and approvals. Additionally, this will be responsible for compiling, analyzing, and reporting of associated Quality and Client metrics. The completion of the Annual Product Quality Review for commercial programs is also required.
The role requires routine interactions with all functions supporting the external network, including interaction with functions across our company's global network.
The role supports activities to ensure systems and business processes are robust, effective, and efficient to comply with required regulations, policies, and guidelines governing the manufacture and holding of materials for our company.
Position Responsibilities:
  • Provides interface between KBI Quality and client regarding batch status, Quality metrics, and Quality issues impacting batch disposition and disposition timeline.
  • Communicates client concerns to KBI teams; facilitates discussions as necessary to resolve client issues. Escalates issues to leadership as needed.
  • Routinely interfaces with the PMO team to ensure any Quality topics are addressed.
  • Serves as QA facilitator for the Quality aspect of all projects requiring QA support. Serves as the accountable Quality lead, decision maker, and delegate for project teams and in related meetings.
  • Supports audit / inspection readiness of the site. Participates in regulatory and other quality and compliance report-outs; reviews client audit outcomes to ensure appropriate corrective actions are implemented as assigned.
  • Serves as client liaison and quality representative on behalf of KBI in audits, client and other client facing meetings and those requiring a Quality SME where the job skills and proficiencies allow.
  • Supports Deviation Management activities by participating in investigational meetings, activities, writing as needed, and approving investigations. Leads Product and Client Complaint activities in accordance with SOP and established requirements.
  • Supports efforts to ensure organization operates within established policies/procedures and complies with all applicable governmental regulations (cGMP, etc.), both domestic and foreign.
  • Operates in a safe and efficient manner and in compliance with the safety and health policy.

Minimum Requirements:
  • BS/BA Degree in Science or Engineering relevant to the pharmaceutical / Life Science or related industries AS/AA acceptable with 7-10 years of relevant experience as described below.
  • Minimum 5 years prior experience in the Pharmaceutical/Biotechnology industry with a thorough knowledge of Quality Systems, Quality Assurance and Quality Control including solid knowledge of global GMP Quality and Regulatory requirements.
  • Minimum of 2 years of previous experience in QA and experience in a Client-Facing QA role. Project Management experience or formal training is a plus.
  • Demonstrates solid Body of Knowledge of Quality systems and functions supporting drug or related FDA governed manufacturing obtained from professional Quality roles. Includes a balance of, from such areas as Supplier Quality Assurance, Compliance, Audits/Inspections, Shop Floor Support, Batch / Material release, Quality document control, review and approval, Validation, QC, Deviations, Prior direct regulatory agency, and audit management /r support experience a plus.
  • Ability to work effectively with others and communicate in customer-facing forums to progress issues and obtain positive results. Able to navigate conflict to achieve deliverables and drive to targeted outcomes. Ability to resolve differing perspectives with effective negotiation.
  • Ability to work professionally and facilitate positive interdepartmental interactions with a diverse group of people. Voluntarily communicates needs and suggestions clearly and effectively. Listens and is attentive to others' ideas and contributions.
  • Demonstrated ability to keep Project Leads, such as PMs and team members informed of the status of assigned work. Ability to determine where escalation is necessary. Capability of being flexible as required tasks change and maintain productivity
  • Demonstrated ability to be a strong, dependable team-player, yet effective at advancing assignments and projects independently.
  • Demonstrated strong attention to detail and effective investigation, problem solving and organizational skills.
  • Ability to properly prioritize tasks, manage time effectively. Positive proactive approach to drive projects/tasks to completion.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.