... Reliance v2020 (QMS), Genesis v2.0, MESA ViewPoint v1.4.3, MPort v3.2, ITS Data Warehouse ... As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP.
... Reliance v2020 (QMS), Genesis v2.0, MESA ViewPoint v1.4.3, MPort v3.2, ITS Data Warehouse ... As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP.
Veeva Safety Consultant Location: Remote (EST Hours - USA) Long Term Contract We are seeking a ... Experience with Veeva Vault QMS, RIM, or eTMF . * Familiarity with GxP compliance and validation ...
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Veeva Safety Consultant Location: Remote (EST Hours - USA) Long Term Contract We are seeking a ... Experience with Veeva Vault QMS, RIM, or eTMF . * Familiarity with GxP compliance and validation ...
... Reliance v2020 (QMS), Genesis v2.0, MESA ViewPoint v1.4.3, MPort v3.2, ITS Data Warehouse ... As an experienced Verification & Validation Test Lead Senior Consultant you will have the ability ...
... Reliance v2020 (QMS), Genesis v2.0, MESA ViewPoint v1.4.3, MPort v3.2, ITS Data Warehouse ... As an experienced Verification & Validation Test Lead Senior Consultant you will have the ability ...
Senior Product Manager - Vault QMS
San Francisco, CA · On-site
$120 - $200/hr
The Role The Vault QMS product team is looking for an all-star Senior Product Manager to define ... You will work closely with customers, sales, consulting, and engineering teams and results will ...
Senior Product Manager - Vault QMS
San Francisco, CA · On-site
$120 - $200/hr
The Role The Vault QMS product team is looking for an all-star Senior Product Manager to define ... You will work closely with customers, sales, consulting, and engineering teams and results will ...
Key ResponsibilitiesLead supplier development and crisis management activitiesConduct QMS and ... consulting workIndividuals who can confidently lead teams, hold accountability, and influence ...
Quick apply
Key ResponsibilitiesLead supplier development and crisis management activitiesConduct QMS and ... consulting workIndividuals who can confidently lead teams, hold accountability, and influence ...
Conduct QMS and process audits to IATF 16949 and/or VDA 6.3 standards * Support APQP, PPAP, and ... Professionals seeking project-based 1099 consulting work * Individuals who can confidently lead ...
Conduct QMS and process audits to IATF 16949 and/or VDA 6.3 standards * Support APQP, PPAP, and ... Professionals seeking project-based 1099 consulting work * Individuals who can confidently lead ...
Conduct QMS and process audits to IATF 16949 and/or VDA 6.3 standards * Support APQP, PPAP, and ... Professionals seeking project-based 1099 consulting work * Individuals who can confidently lead ...
Conduct QMS and process audits to IATF 16949 and/or VDA 6.3 standards * Support APQP, PPAP, and ... Professionals seeking project-based 1099 consulting work * Individuals who can confidently lead ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare Enterprise Operations ... Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs ...
Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results ... Lead requirements workshops, design, prototype, configure and document content management/QMS data ...
Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results ... Lead requirements workshops, design, prototype, configure and document content management/QMS data ...
Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results ... Lead requirements workshops, design, prototype, configure and document content management/QMS data ...
Quick apply
Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results ... Lead requirements workshops, design, prototype, configure and document content management/QMS data ...
Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results ... Lead requirements workshops, design, prototype, configure and document content management/QMS data ...
Clarkston Consulting is seeking motivated, self-driven leaders who are energized by team results ... Lead requirements workshops, design, prototype, configure and document content management/QMS data ...
Qms Consultant information
See salary details
$26.42 is the 25th percentile. Wages below this are outliers.
$24.28 - $28.61
51% of jobs
$28.61 - $32.93
0% of jobs
$32.93 - $37.26
11% of jobs
$37.26 - $41.59
12% of jobs
$41.59 - $45.91
0% of jobs
$45.91 - $50.24
1% of jobs
$51.32 is the 75th percentile. Wages above this are outliers.
$50.24 - $54.57
5% of jobs
$54.57 - $58.89
5% of jobs
$58.89 - $63.22
5% of jobs
$63.22 - $67.55
5% of jobs
$67.55 - $71.88
5% of jobs
$24
$40
$71
How much do qms consultant jobs pay per hour?
What is a QMS consultant?
A QMS (Quality Management System) Consultant helps organizations develop, implement, and improve their quality management systems to comply with industry standards such as ISO 9001. They assess current processes, identify areas for improvement, and provide guidance to ensure regulatory compliance and operational efficiency. Their role includes documentation, training, audits, and continuous improvement strategies to enhance product or service quality.
What are the key skills and qualifications needed to thrive as a QMS consultant?
To thrive as a QMS Consultant, you need a deep understanding of quality management systems (such as ISO 9001), process improvement methodologies, and strong analytical abilities, typically supported by a relevant degree and QMS certifications. Familiarity with tools like corrective and preventive action (CAPA) software, internal audit systems, and document control platforms is often required. Excellent communication, project management, and problem-solving skills help consultants effectively engage with diverse teams and clients. These skills and qualities ensure the successful development, implementation, and continual improvement of quality management systems for organizations.
What are the typical daily responsibilities of a QMS consultant?
As a QMS Consultant, your daily responsibilities may include reviewing and improving organizational processes, conducting internal audits, advising on compliance with relevant standards like ISO 9001, and developing quality documentation. You may also lead training sessions, facilitate corrective and preventive action initiatives, and collaborate closely with different department heads to implement effective quality solutions. Additionally, you'll be tasked with identifying areas for continuous improvement and ensuring best practices are communicated across the organization. This role offers a mix of hands-on problem-solving and strategic planning, making it both dynamic and impactful.

Deloitte rating
8.2
Based on 92 frontline employees who took The Breakroom Quiz
45th of 150 rated financial services
Job description
Recruiting for this role ends on 9/11/2026
Work you'll do/Responsibilities
The Verification & Validation Test Lead Senior Consultant will lead the Verification & Validation (V&V) activities for a Hayward, CA manufacturing site - an 8-application GMP portfolio (all High priority) including TrakSYS v3.1 (MES), EtQ Reliance v2020 (QMS), Genesis v2.0, MESA ViewPoint v1.4.3, MPort v3.2, ITS Data Warehouse, Subversion, and Acronis. The candidate must bring hands-on V&V lifecycle experience (IQ/OQ/PQ), 21 CFR Part 11 and GAMP 5 compliance knowledge, and the ability to lead site-based stakeholder communication in a cGMP drug-device manufacturing environment. Act as the onsite V&V testing representative at the Hayward CA site, building trusted relationships with site quality, engineering, and application owners. Execute V&V lifecycle activities (IQ/OQ/PQ) for validated manufacturing systems - MES (TrakSYS), QMS (EtQ Reliance), process control (Genesis), plant dashboards (MESA ViewPoint), and data integration (MPort). Author and execute V&V protocols, test scripts, and summary reports aligned to CSV/CSA methodology and risk-based testing framework. Ensure all V&V documentation meets 21 CFR Part 11, cGMP, and GAMP 5 standards including electronic records, audit trail verification, and data integrity (ALCOA++) compliance. Lead UAT and qualification coordination - organizing sessions, aligning business testers and quality reviewers, and driving sign-off. Manage defect and deviation lifecycle with clear stakeholder communication on status, severity triage, and closure timelines. Support CAPA, change control, and periodic review activities for validated manufacturing systems. Deliver regular V&V status reports and qualification readiness updates to Hayward site stakeholders and central Testing Shared Services team. The successful candidate would possess these skills:
- Ability to work independently and collaborate as part of a team
- Effective written and verbal communication skills
- Meticulous attention to detail and quality of work product
- Ability to build and sustain professional relationships
- Ability to lead projects or workstreams
- Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
- Strong interpersonal skills and professional demeanor
- Ability to meet deadlines
- Ability to provide clear guidance to others
AI & Engineering leverages cutting-edge engineering capabilities to build, deploy, and operate integrated/verticalized sector solutions in software, data, AI, network, and hybrid cloud infrastructure. These solutions are powered by engineering for business advantage, transforming mission-critical operations. We enable clients to stay ahead with the latest advancements by transforming engineering teams and modernizing technology & data platforms. Our delivery models are tailored to meet each client's unique requirements
Our Industry Solutions offering provides verticalized solutions that transform how clients sell products, deliver services, generate growth, and execute mission-critical operations. We deliver integrated business expertise with scalable, repeatable technology solutions specifically engineered for each sector.
Qualifications Required
- 5+ years of executing V&V lifecycle activities (IQ/OQ/PQ) for validated manufacturing systems - MES (TrakSYS), QMS (EtQ Reliance), process control (Genesis), plant dashboards (MESA ViewPoint), and data integration (MPort).
- Author and execute V&V protocols, test scripts, and summary reports aligned to CSV/CSA methodology and risk-based testing framework.
- Ensure all V&V documentation meets 21 CFR Part 11, cGMP, and GAMP 5 standards including electronic records, audit trail verification, and data integrity (ALCOA++) compliance.
- Manage defect and deviation lifecycle with clear stakeholder communication on status, severity triage, and closure timelines.
- Support CAPA, change control, and periodic review activities for validated manufacturing systems.
- Bachelor's degree, preferably in information technology, business, or healthcare related field; or equivalent experience
- Limited immigration sponsorship may be available
- Ability to travel 10%, on average, based on the work you do and the clients and industries/sectors you serve
You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance.
Deloitte is committed to providing reasonable accommodations for people with disabilities. If you require a reasonable accommodation to participate in the recruiting process, please direct your inquiries to the Global Call Center (GCC) at USTalentCICInbox@deloitte.com.
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Benefits
At Deloitte, we know that great people make a great organization. We value our people and offer employees a broad range of benefits. Learn more about what working at Deloitte can mean for you.
Our people and culture
Our inclusive culture empowers our people to be who they are, contribute their unique perspectives, and make a difference individually and collectively. It enables us to leverage different ways of thinking, ideas, and perspectives, and bring more creativity and innovation to help solve our clients' most complex challenges. This makes Deloitte one of the most rewarding places to work.
Our purpose
Deloitte's purpose is to make an impact that matters for our people, clients, and communities. At Deloitte, purpose is synonymous with how we work every day. It defines who we are. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities. Learn more.
Professional development
From entry-level employees to senior leaders, we believe there's always room to learn. We offer opportunities to build new skills, take on leadership opportunities and connect and grow through mentorship. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP. Please see https://www.deloitte.com/us/about for a detailed description of the legal structure of Deloitte LLP and its subsidiaries.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.
Requisition code: 358937
Job ID 358937