Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
... QA/RA, and the executive team. What you'll own: Manufacturing controls and process implementation specific to medical-grade products - while maintaining operational velocity Global (OUS ...
... QA/RA, and the executive team. What you'll own: Manufacturing controls and process implementation specific to medical-grade products - while maintaining operational velocity Global (OUS ...
Led QA for GMP drug manufacturer, has qualified vendor analytical assays * Vendor-side, taking scientific instruments from R&D into GMP-ready state for pharma/biotech customers. * Uses right-sized ...
Led QA for GMP drug manufacturer, has qualified vendor analytical assays * Vendor-side, taking scientific instruments from R&D into GMP-ready state for pharma/biotech customers. * Uses right-sized ...
QA RA Director Consulting Position
Raleigh, NC · On-site
$180 - $240/hr
Led QA for GMP drug manufacturer, has qualified vendor analytical assays Vendor‑side, taking scientific instruments from R&D into GMP-ready state for pharma/biotech customers. * Uses right‑sized ...
New
QA RA Director Consulting Position
Raleigh, NC · On-site
$180 - $240/hr
Led QA for GMP drug manufacturer, has qualified vendor analytical assays Vendor‑side, taking scientific instruments from R&D into GMP-ready state for pharma/biotech customers. * Uses right‑sized ...
New
Led QA for GMP drug manufacturer, has qualified vendor analytical assays * Vendor-side, taking scientific instruments from R&D into GMP-ready state for pharma/biotech customers. * Uses right-sized ...
Led QA for GMP drug manufacturer, has qualified vendor analytical assays * Vendor-side, taking scientific instruments from R&D into GMP-ready state for pharma/biotech customers. * Uses right-sized ...
Senior Specialist, GMP Quality Assurance
$89K - $122K/yr
The Senior Specialist, GMP Quality Assurance will collaborate internally with QA, RA, and CMC departments. As needed, work with external Approved Service Providers to ensure oversight and compliance.
Senior Specialist, GMP Quality Assurance
$89K - $122K/yr
The Senior Specialist, GMP Quality Assurance will collaborate internally with QA, RA, and CMC departments. As needed, work with external Approved Service Providers to ensure oversight and compliance.
Collaborate with external service providers and internally with QA, RA, CMC teams to support the timely review and approval of documents * Review records including audit trails and ensure integrity ...
Collaborate with external service providers and internally with QA, RA, CMC teams to support the timely review and approval of documents * Review records including audit trails and ensure integrity ...
The QA/RA Manager provides hand-on experience in Regulatory Affairs and Quality Management Systems. This includes projects and daily tasks associated with maintaining compliance with domestic quality ...
The QA/RA Manager provides hand-on experience in Regulatory Affairs and Quality Management Systems. This includes projects and daily tasks associated with maintaining compliance with domestic quality ...
The QA/RA Manager provides hand-on experience in Regulatory Affairs and Quality Management Systems. This includes projects and daily tasks associated with maintaining compliance with domestic quality ...
Quick apply
The QA/RA Manager provides hand-on experience in Regulatory Affairs and Quality Management Systems. This includes projects and daily tasks associated with maintaining compliance with domestic quality ...
Director of Regulatory Affairs and Quality Assurance (RA / QA)
San Francisco, CA · On-site
$180 - $240/hr
We are looking for a Director of Regulatory Affairs and Quality Assurance to help build a business around this opportunity. This role will provide leadership for risk management and oversee the ...
Director of Regulatory Affairs and Quality Assurance (RA / QA)
San Francisco, CA · On-site
$180 - $240/hr
We are looking for a Director of Regulatory Affairs and Quality Assurance to help build a business around this opportunity. This role will provide leadership for risk management and oversee the ...
We are looking for a Director of Regulatory Affairs and Quality Assurance to help build a business around this opportunity. This role will provide leadership for risk management and oversee the ...
Quick apply
We are looking for a Director of Regulatory Affairs and Quality Assurance to help build a business around this opportunity. This role will provide leadership for risk management and oversee the ...
We are looking for a Director of Regulatory Affairs and Quality Assurance to help build a business around this opportunity. This role will provide leadership for risk management and oversee the ...
We are looking for a Director of Regulatory Affairs and Quality Assurance to help build a business around this opportunity. This role will provide leadership for risk management and oversee the ...
Senior Quality Assurance Specialist
Rensselaer, NY · On-site
$103K - $129K/yr
Minimum 8 years QA, RA or Compliance experience in pharmaceutical industry (preferred in APIs) at USFDA regulated facilities * Broad knowledge of cGMP, FDA and international regulations (e.g., 21 CFR ...
Senior Quality Assurance Specialist
Rensselaer, NY · On-site
$103K - $129K/yr
Minimum 8 years QA, RA or Compliance experience in pharmaceutical industry (preferred in APIs) at USFDA regulated facilities * Broad knowledge of cGMP, FDA and international regulations (e.g., 21 CFR ...
Senior Quality Assurance Specialist
Rensselaer, NY · On-site
$103K - $129K/yr
Minimum 8 years QA, RA or Compliance experience in pharmaceutical industry (preferred in APIs) at USFDA regulated facilities * Broad knowledge of cGMP, FDA and international regulations (e.g., 21 CFR ...
Senior Quality Assurance Specialist
Rensselaer, NY · On-site
$103K - $129K/yr
Minimum 8 years QA, RA or Compliance experience in pharmaceutical industry (preferred in APIs) at USFDA regulated facilities * Broad knowledge of cGMP, FDA and international regulations (e.g., 21 CFR ...
Quality Assurance & Regulatory Affairs Manager
Manhattan, NY · On-site
$140 - $150/hr
The QA/RA Manager is responsible for ensuring product quality, safety, and regulatory compliance across a growing, wellness product portfolio. This hands‑on role supports product development ...
New
Quality Assurance & Regulatory Affairs Manager
Manhattan, NY · On-site
$140 - $150/hr
The QA/RA Manager is responsible for ensuring product quality, safety, and regulatory compliance across a growing, wellness product portfolio. This hands‑on role supports product development ...
New
Vice President, Quality Assurance - Regulatory Affairs
San Antonio, TX · On-site
$180 - $280/hr
Lead, coach, and develop a high-performing QA/RA organization * Set clear expectations, accountability, and development pathways for team members * Partner closely with Engineering, Product, Clinical ...
New
Vice President, Quality Assurance - Regulatory Affairs
San Antonio, TX · On-site
$180 - $280/hr
Lead, coach, and develop a high-performing QA/RA organization * Set clear expectations, accountability, and development pathways for team members * Partner closely with Engineering, Product, Clinical ...
New
Specialist / Senior Specialist - Quality Assurance
Lexington, MA · On-site
$107K - $117K/yr
Collaborate with external service providers and internally with QA, RA, CMC teams to support the timely review and approval of documents * Review records including audit trails and ensure integrity ...
Specialist / Senior Specialist - Quality Assurance
Lexington, MA · On-site
$107K - $117K/yr
Collaborate with external service providers and internally with QA, RA, CMC teams to support the timely review and approval of documents * Review records including audit trails and ensure integrity ...
Qa Ra information
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$21.5K - $36.7K
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0% of jobs
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0% of jobs
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14% of jobs
$102.3K is the 25th percentile. Wages below this are outliers.
$97.6K - $112.9K
31% of jobs
The median wage is $114.9K / yr.
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$128.1K - $143.3K
8% of jobs
$143.3K - $158.5K
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$158.5K - $173.8K
3% of jobs
$173.8K - $189K
10% of jobs
$21.5K
$124.1K
$189K
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Senior Consultant - Product Quality & Safety - Life Sciences & Healthcare
Boston, MA • On-site
Full-time
Re-posted 17 days ago
Deloitte rating
8.2
Based on 92 frontline employees who took The Breakroom Quiz
44th of 150 rated financial services
Job description
Enterprise Operations & Risk
Our Deloitte Regulatory, Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory environment into defensible actions that strengthen, protect, and transform their organizations. Join our team and use advanced data, AI, and emerging technologies with industry insights to help clients bring clarity from complexity and accelerate their path to value creation
Work You'll Do
The Senior Consultant is responsible for helping to deliver related client projects, and in doing so to continue to grow professionally in the areas of subject matter expertise and consulting engagement administration. A Senior Consultant must understand how Commercial and Medical activities and related messaging/content are influenced by Regulatory/Health Authority requirements. This could include:
- Support clients in pharmaceutical and medical device Regulatory Affairs and Quality Assurance strategy, operating model, process, and governance improvements
- Conduct quality and regulatory due diligence for mergers & acquisitions (M&A), including risk identification, evidence requests, and diligence readouts (e.g., compliance history, inspection readiness, quality system maturity)
- Support separation and integration activities for QA/RA, including Day 1 readiness, target operating model, transition service agreement (TSA) considerations, and cutover planning
- Assess and remediate quality management system (QMS) and regulatory compliance gaps (e.g., SOPs, training, deviation management, corrective and preventive actions (CAPA), change control, complaints)
- Support inspection readiness planning and execution (e.g., mock inspections, observation response planning, compliance remediation roadmaps)
- Help design and implement RA/QA technology enablement, including requirements definition, vendor selection support, process design, testing/validation coordination, and deployment/adoption planning
- Support implementation and optimization of systems such as electronic QMS (eQMS), document management systems (DMS), learning management systems (LMS), complaint handling, CAPA, change control, audit management, supplier quality, and regulatory information management (RIM) platforms
- Develop client-ready deliverables (assessments, workflows, requirements, business cases, implementation plans, and executive communications) and manage workstream risks, dependencies, and stakeholder alignment
- Additional expectation is to continually build detailed subject matter expertise and assist in the buildout of service offerings in the area of Commercial and Medical Content Management
Our Enterprise Operations & Risk offering enables clients to achieve profitable growth and competitive advantage by optimizing "heart of the business" operations. We leverage deep domain expertise to extend enterprise resilience, agility and remediation. Our professionals address client needs which span the organization and impact strategy, operations, performance and reputation.
Qualifications
Required:
- Bachelor's degree required
- 5+ years of experience with a focus on Life Sciences in a Consulting or Industry role.
- Experience in the application of artificial intelligence (AI) tools and techniques to deliver measurable business outcomes (e.g., automation, analytics, decision support)
- Experience in pharmaceutical QA/RA (e.g., Good Manufacturing Practice (GMP), quality systems, compliance remediation) and/or medical device QA/RA (e.g., design controls, risk management, post-market processes)
- Working knowledge of common regulatory/quality expectations and frameworks applicable to pharma and devices (tailor to your target market)
- Experience translating regulatory/quality requirements into operational processes, controls, and measurable performance metrics
- Experience supporting M&A due diligence focused on QA/RA (planning, data room requests, interviews, risk rating, and diligence reporting)
- Experience supporting separation and integration for QA/RA functions (process and system disentanglement, integration design, governance, TSA planning, and cutover execution)
- Ability to identify and quantify quality/regulatory risks that impact deal value (e.g., remediation cost, timeline, supply risk, launch/approval risk)
- Experience implementing or optimizing quality and regulatory systems, including requirements gathering, future-state process design, validation approach coordination, testing, training, and go-live support
- Familiarity with eQMS and RIM capabilities such as document control, training, deviations, CAPA, change control, audits, complaints, supplier quality, and submission/product registration data management
- Experience with data and reporting for QA/RA (e.g., dashboards, KPIs, traceability, audit trails), including adoption and sustainment planning
- Experience in Project Management
- Experience working in a mandated deadline environment and ability to work effectively on multiple client assignments
- High accuracy rate and attention to detail; ability to produce client-ready deliverables to a high-level executive/professional client base
- Experience leading/mentoring a cross functional team of government program consultants
- Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future.
- Ability to travel up to 50%, based on the work you do and the clients and industries/sectors you serve.
• 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
Preferred:
- 3+ years of experience in the Pharmaceutical, Biotech and/or Medical Device industries
The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $110700- $218300.
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 fac tors, 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.
Recruiting tips
From developing a stand out resume to putting your best foot forward in the interview, we want you to feel prepared and confident as you explore opportunities at Deloitte. Check out recruiting tips from Deloitte recruiters.
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 Financial Advisory Services LLP, a subsidiary of Deloitte LLP. Please see www.deloitte.com/us/about for a detailed description of the legal structure of Deloitte LLP and its subsidiaries. Certain services may not be available to attest clients under the rules and regulations of public accounting.
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.
Qualified applicants with criminal histories, including arrest or conviction records, will be considered for employment in accordance with the requirements of applicable state and local laws, including the Los Angeles County Fair Chance Ordinance for Employers, City of Los Angeles's Fair Chance Initiative for Hiring Ordinance, San Francisco Fair Chance Ordinance, and the California Fair Chance Act. See notices of various fair chance hiring and ban-the-box laws where available. Fair Chance Hiring and Ban-the-Box Notices | Deloitte US Careers
Requisition code: 350400
Job ID 350400
About Deloitte
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Industry
Finance and insurance
Company size
10,000+ Employees
Headquarters location
Orlando, FL, US