Title: Manager, Quality Engineering & AI Validation Location: Atlanta; Boston; Charlotte; Chicago; Dallas; Los Angeles; New York; San Francisco Hybrid Job Description: Please note: This position is not eligible for immigration sponsorship. Company Overview We are the better way to work in finance. As private equity’s value creation partner, we sit at the heart of PE—where sponsors and CFOs meet. Through financial consulting rooted in data, technology, and AI, we help clients drive value—supporting the office of the CFO to drive end-to-end value creation. If you crave challenging work and are looking to grow, come solve complex issues alongside 1,600+ finance & technology experts in a supportive, collaborative environment. Backed by premier private equity firms and headquartered in New York with 11 offices around the globe, we are a high-growth, entrepreneurial firm looking for people who want to be part of building something great. Come make your mark. Manager, Quality Engineering and AI Validation The Manager of Quality Engineering and AI Validation leads Accordion's centralized Quality Engineering and AI Validation function across software delivery pods. This impactful role will be critical in owning the quality operating model, release-readiness standards, test strategy, AI validation framework, and quality metrics used to support both conventional software and AI-enabled solutions. Above all, this leader will ensure quality is designed into delivery from the start, not inspected in at the end. This position will ideally be based in one of our US offices and is a hybrid role with the flexibility to work remotely 2 days per week (also eligible for remote candidates). This position is not eligible for immigration sponsorship. What You’ll Do: Quality Strategy & Governance - Define the firm-wide quality strategy, release gates, and validation standards across development pods - Establish a risk-based quality model for traditional software and AI-enabled workflows - Define when pod-level validation is sufficient and when independent QA validation is required AI Validation Leadership - Build and operationalize the QA approach for AI-led products, including benchmark datasets, scoring rubrics, regression comparisons, and grounded-output validation - Establish testing expectations for instruction adherence, consistency, business correctness, control compliance, and hallucination risk - Partner with Engineering and Product leaders on quality implications of prompt, model, workflow, and tooling changes - Team Leadership - Lead and develop quality engineers, AI quality analysts, and domain-oriented QA resources - Improve the maturity of automation, evaluation routines, test evidence standards, and release discipline - Create a scalable central model that supports pods without becoming a bottleneck Finance & Risk Alignment - Partner with Finance and practice SMEs to ensure solutions are validated against real business use, materiality, and control expectations - Ensure high-risk workflows receive the right level of domain review before production release Production Quality - Define the framework for production quality monitoring, including escaped defects, output-quality degradation, reviewer overrides, and control failures - Create visibility into quality trends, readiness, and recurring failure patterns for Engineering and leadership You Have: - 8+ years of QA, software testing, or quality engineering experience, including team leadership – you are a builder of quality systems and operating models - Deep fluency in both engineering quality and business impact - Experience building test strategy, release-readiness processes, and automation programs in modern software environments - Experience supporting AI-enabled applications, workflow automation, data products, or decision-support systems - Strong understanding of functional, integration, regression, API, and data validation approaches - Ability to translate business-critical finance workflows into quality controls and release criteria - Comfortability asking tough questions about readiness, risk, and evidence - Strong communication skills and credibility with Engineering, Product, and business stakeholders – you are structured, pragmatic, and highly credible - Consistent focus on trust, traceability, and scalable execution - Bachelor's degree preferred You Are: - Excited to be part of a growing team, with a focus on driving future growth - Passionate about delivering exceptional client service - Knowledgeable about the relationship between Private Equity sponsors and their portfolio companies, particularly within the office of the CFO - Willing to get your hands dirty in the details of a project while simultaneously seeing the whole picture - Comfortable managing projects with multiple complex workstreams while also focused on your single workstream (you are managing and doing) - A self-starter with a strong work ethic - Full of entrepreneurial spirit and comfortable in a fluid, flat organization - Able to effectively communicate complex issues and solutions, and raise issues to senior team members when necessary - A team player, able to work with team members across all levels - Someone who enjoys mentoring others and doing meaningful work - A leader of others; you lead by example The annual salary for this role ranges from: $165,000 to $205,000 + benefits + bonus. Actual compensation packages are determined by evaluating a wide array of factors unique to each candidate, including but not limited to geographic location, skill set, years and depth of experience, education, certifications, cost of labor and internal equity. Accordion is an Equal Opportunity Employer. We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical​​​ condition, pregnancy, genetic information, gender, sexual orientation, gender identity or ​expression, veteran status, or any other status protected under federal, state, or local law.

• Identify, isolate, document and fix any localization / linguistic issues • Follow and complete Test Cases / Checklists • Write bug descriptions based on company standards • Collaborate with partner teams in testing the product

Role Description A leading industrial engineering business is seeking a detail-oriented Quality & Compliance professional to take ownership of key safety and quality systems. This role will oversee compliance platforms, non-conformance tracking, ISO standards, and document control processes while supporting audits and continuous improvement initiatives. The ideal candidate will have strong experience in quality assurance within an industrial or manufacturing environment and a hands-on approach to maintaining accurate, compliant, and efficient systems across the business. Key Responsibilities - Safety, Compliance & Systems Management - Take ownership of the HSI Donesafe platform, managing safety, compliance, and non-conformance reporting workflows. - Manage document control processes across the business, including version control, accessibility, and audit readiness. - Coordinate and maintain confined space registers, ensuring compliance with safety standards and regular review cycles. - Drive adherence to quality processes across the business, ensuring consistency in documentation, reporting, and operational practices. - Support audit preparation and compliance activities, ensuring the business meets regulatory and certification requirements. - Quality Assurance & ISO Compliance - Maintain and manage the non-conformance register, ensuring all issues are logged, tracked, and closed out in a timely manner. - Oversee quality assurance documentation, ensuring all records are accurate, up to date, and compliant with internal and external requirements. - Conduct gap analyses against ISO standards and internal quality frameworks, identifying areas for improvement. - Support the implementation and continuous improvement of quality management systems and processes. - Documentation & Technical Requirements - Prepare, review, and maintain SWMS (Safe Work Method Statements) for client and project requirements. - Work closely with operational teams to ensure defects, measurements, and quality checks are properly recorded and actioned. - Perform a high volume of administrative and documentation tasks with accuracy and consistency. - Develop and implement training plans related to quality, safety, and compliance requirements. - Identify process gaps and support continuous improvement initiatives. - Other role-specific duties as they arise. Qualifications - Bachelor’s degree in Engineering, Quality Management, Business, or a related field. - At least 2–5 years of experience in a quality control, quality assurance, or compliance-focused role within an industrial, manufacturing, or engineering environment. - Strong experience working with safety and compliance systems (e.g. HSI Donesafe or similar platforms). - Experience managing non-conformance registers and quality reporting processes. - Solid understanding of ISO standards and quality management systems (e.g. ISO 9001). - Proven ability to manage document control processes in a structured and compliant manner. - Experience preparing and reviewing SWMS and other safety-related documentation. - Strong administrative capability, with the ability to handle repetitive and detail-heavy tasks accurately. - High attention to detail and strong organisational skills. - Ability to identify process gaps and support continuous improvement initiatives. - Strong written communication skills for documentation, reporting, and compliance records. - Ability to work independently and take ownership of quality and compliance functions. - Experience within a pump, mechanical, or industrial equipment environment is highly advantageous. - Exposure to SAP-based safety or compliance systems is desirable. - Experience supporting or leading ISO audits and certification processes is a plus. - Experience developing and delivering internal training programs is also advantageous. Benefits - Work from home - Mon - Fri: 7:30 AM – 4:30 PM PHT (adjustments will be made for daylight saving time) - HMO with 2 free dependents and medical reimbursements - Government-mandated benefits - WFH allowances - Opportunities to work with leading companies in Australia and beyond - Training programmes for career development - Engaging company outings, team activities and wellness sessions - Supportive, inclusive culture - Dedicated managers focused on your growth and success Company Description Twoconnect connects highly skilled Filipino professionals with established companies in Australia, New Zealand, the United States, the United Kingdom and Europe, providing direct access to global careers and long-term opportunities. - We offer competitive pay and benefits, additional entitlements and structured career development programs that make employment both financially rewarding and professionally sustainable. - Our industry-leading retention rate demonstrates our commitment to a people-first culture that prioritizes stability, growth and genuine care for every employee. - Twoconnect is an equal opportunity employer. We value cultural diversity and foster an inclusive workplace where every employee is respected and supported as part of a growing global team.

Title: Quality Technical Specialist Location: United States Work Type: Remote, Full Time Job ID: R-172818 Job Description: The Opportunity: Avantor is looking for a Quality Technical Specialist to join us! The Specialist supports quality assurance operations by ensuring compliance with standards and regulations, contributing to testing and process improvements, supporting audits and corrective actions, and collaborating with internal teams and suppliers to resolve quality issues. This is a remote role that can be based in the U.S. What we're looking for - Education: BS/BA Degree in Biology, Biotechnology, Bio Engineering, Chemistry, Chemical Engineering, or related field required - Experience: Minimum of three (3) years of combined experience in technical services, engineering, quality or sales in chemical or pharmaceutical environment required - Synthetic pharmaceutical & biopharmaceutical drug development and manufacturing as well as an understanding of industry regulations (cGMP, FDA, ICH, and WHO), quality and validation. - Quality and process engineering in a chemical or pharmaceutical environment. - Collaboration Tool: Excellent knowledge of Microsoft Office Suite; experience working with other computer applications (such as databases) with an aptitude to further develop technical skills preferred - Preferred Qualifications: - Hands-on experience in a laboratory or manufacturing environment - Project management experience - Experience in at least one of the following areas is highly desired How you will thrive and create an impact The Quality Technical Specialist provides technical and quality support to Avantor's global customer and sales organizations. This role partners with internal teams to research, compile, and communicate information related to Avantor's pharmaceutical and laboratory product offerings. The Specialist is also responsible for developing and maintaining quality documentation, updating product and customer databases, and managing customer Quality Agreements. - Manage and negotiate Customer Quality Agreements in collaboration with the Avantor legal team. - Responds to customers' technical and quality inquiries (via telephone and email,) pertaining to the Company's pharmaceutical and laboratory product lines which includes excipients, bio reagents, salts, sugars, acids, cGMP-manufactured solutions and chromatography media as they relate to quality agreement support. - Researches technical documents, reviews product specifications, and utilizes resources such as technical monographs, Company R&D experts, in-house databases and personal technical background to prepare quality agreements and communicate information to customers. - Participates in designing/improving quality agreement information collection and archiving processes with other departments including but not limited to Marketing, Sales, and Quality Assurance. - Participates in lean principles review of processes in order to maximize team efficiency in customer responses. - Participates as part of cross functional team associated with the customer intimacy programs; responsibilities may include project management, data collection and review, hosting and participating in recurring meetings. - Performs other duties as assigned with or without accommodation. KNOWLEDGE SKILLS AND ABILITIES (Those necessary to perform the job competently) - Demonstrated ability to manage multiple priorities in a fast-paced environment while keeping customers' needs in mind. - Results-oriented, energetic, self-motivated, and a dedicated team player. - Proven problem solving and leadership skills. - Exhibits initiative, attention to details and follow-through. - Ability to learn industry regulations and Avantor's proprietary systems. - Committed to the highest standards of customers satisfaction and providing the ultimate customer experience. - Excellent verbal, written skills in addition to presentation and interpersonal communication skills. ENVIRONMENTAL WORKING CONDITIONS & PHYSICAL EFFORT (Under Typical Positions) The work environment is an office setting. The duties of the job may require the Quality Technical Specialist to go to the manufacturing facility and R&T building on occasion. Occasional travel may be required both domestically and internationally. #LI-Remote Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor? Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents Pay Transparency: The expected pre-tax pay for this position is Actual pay may differ depending on relevant factors such as prior experience and geographic location. EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. 3rd Party Non-Solicitation Policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation. Avantor offers a comprehensive benefits package including medical, dental, and vision coverage, wellness programs, health savings and flexible spending accounts, a 401(k) plan with company match, and an employee stock purchase program. Employees also receive 11 paid holidays, accrue 18 PTO days annually, are eligible for volunteer time off and 6 weeks of 100% paid parental leave (except in states that offer paid family leave). These benefits may not apply to employees covered by a collective bargaining agreement or those subject to other eligibility rules.