Top 142 Analytical validation manager Jobs in Wake Forest, Nc

QA Systems Manager
Guerbet —Raleigh, NC
- Full-time
- 7 years
- Analysis skills
- Doctor of Philosophy
Systems Analyst IV
Guerbet —Raleigh, NC
- Full-time
- Hybrid work
- Oracle
- Analysis skills
- Bachelor's degree
10d
Associate Dean, Financial Aid Technology, Reporting and Training
Wake Technical Community College —Raleigh, NC
- $82,200 - $102,756 a year
- Full-time
- 3 years
- Master's degree
- SQL
- Paid holidays
- Disability insurance
Senior Construction Performance Analyst
McGough Construction —Raleigh, NC
- Hybrid work
- 7 years
- Office
- SQL
13d
Quality Technical and Validation Manager
GlaxoSmithKline —Zebulon, NC
- Full-time
- Hybrid work
- 7 years
- Bachelor of Science
- Analysis skills
13d
Manager, Clinical Labs - External Referral Lab
Duke Health —Durham, NC
- Full-time
- 7 years
- Bachelor's degree
- Senior level
HR Manager
Opal Hotels Group —Raleigh, NC
- $80,000 - $90,000 a year
- Full-time
- OSHA
- Customer service
- Hotel
Quick Apply
Manager, Payroll N.A.
Wasserman Media Group LLC —Raleigh, NC
- $110,000 - $125,000 a year
- Full-time
- 5 years
- Finance
- Analysis skills
- Commuter assistance
- Paid parental leave
Senior/Commercial Pricing and Contracting Manager, Market Access
United Therapeutics —Research Triangle Park, NC
- $121,000 - $190,000 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- 6 years
- Paid parental leave
- Employee stock purchase plan
Regulatory Compliance Lead
GlaxoSmithKline —Zebulon, NC
- Full-time
- Bachelor of Science
- 8 years
- Bachelor's degree
13d
Senior Consultant - Clinical Documentation Specialist
Deloitte —Raleigh, NC
- $110,700 - $218,300 a year
- Full-time
- Microsoft Word
- Nursing
- RN License
Manager, Financial Crimes Oversight Testing U.S.
Royal Bank of Canada —Raleigh, NC
- $70,000 - $130,000 a year
- Full-time
- Writing skills
- Mid-level
- Office
- Disability insurance
- Health insurance
Technology Incubation – Early Stage Product Manager
Lenovo —Morrisville, NC
- $180,000 - $210,000 a year
- Full-time
- Remote
- Computer Science
- Mid-level
- 8 years
MSAT Technical Lead – Drug Substance (Sr Manager)
Sobi —Morrisville, NC
- $140,000 - $165,000 a year
- Full-time
- Remote
- 3 years
- Team management
- Travel
- Health insurance
- Dental insurance
Quick Apply
Martech Developer- Manager
PRICE WATERHOUSE COOPERS —Raleigh, NC
- $73,500 - $244,000 a year
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Paid holidays
- Health insurance
Business Development Associate - Pharmaceutical
Ecolab Inc. —Raleigh, NC
- $93,800 - $140,600 a year
- Overtime
- Research
- Mid-level
- Bachelor's degree
- Opportunities for advancement
ERP Data Management Lead
GlaxoSmithKline —Zebulon, NC
- Full-time
- Hybrid work
- Oracle
- Word processing
- Bachelor of Science
HR & Benefits Analyst
Audemars Piguet —Raleigh, NC
- Full-time
- Hybrid work
- 5 years
- Analysis skills
- Project management
Quick Apply
Marketing Engagement Associate Manager
Accenture —Raleigh, NC
- $68,300 - $182,600 a year
- Full-time
- Remote
- Marketing
- Writing skills
- Analysis skills
- Paid holidays
- Disability insurance
Production Supervisor - 2nd Shift
Indivior —Raleigh, NC
- $100,000 - $115,000 a year
- Full-time
- 5 years
- Computer literacy
- Basic math
- Profit sharing
- Employee stock purchase plan

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analytical validation manager jobs near wake forest, nc

QA Systems Manager

Guerbet -
Raleigh, NC

Apply Now

Job Details

Full-time

Qualifications

Regulatory inspections
Drug regulation
Quality control audit
Pharmaceutical company experience
ICH Q10
Biomedical regulatory compliance
Quality audits
FDA regulations
Audit support
Pharmaceutical manufacturing facility experience
Analytics

Full Job Description

At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 100 years, we continuously innovate to improve the diagnosis, prognosis and quality of life of patients.

Customer Centricity, Cooperation, Audacity, Focus, and Responsibility are the values that we share and practice on a daily basis.

Working at Guerbet is not only being part of a multicultural team with nearly 3,000 people across more than 20 countries, but it is above all about playing a unique role in the future of medical imaging.

WHAT WE ARE LOOKING FOR

The Quality Systems Manager will be operating in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for.

The Quality Systems Manager is responsible for overseeing the execution and continuous improvement of Guerbet's Quality Management System (QMS). This role ensures compliance with global regulatory requirements (e.g., FDA, EMA, ANVISA, PIC/S), supports GMP operations, and drives a culture of quality across the organization. The manager will lead cross-functional initiatives to enhance documentation, training, change control, Data Integrity, Supplier Management, APQR management, Risk Management, Supplier Quality and audit readiness. The incumbent will coach and develop their Direct Reports supporting the site's continuous improvement initiatives.

YOUR ROLE

Quality System Oversight

Own, maintain, and continuously improve core Quality Management System (QMS) elements as defined in the role scope.
Ensure QMS processes remain compliant, efficient, and aligned with current regulatory expectations (e.g., FDA, EU GMP).
Lead periodic review and revision of SOPs, policies, and quality manuals to ensure accuracy and effectiveness.

Governance & Metrics

Collaborate with Functional Area Leaders and Operational Excellence (OpEx) to define and monitor leading and lagging quality performance indicators.
Analyze key performance indicators (KPIs) (e.g., change control cycle time) and drive continuous improvement actions.
Present quality system performance metrics to senior leadership with recommendations for improvement.
Chair or support Quality Governance forums, including Change Control Review Board meetings.

Audit & Inspection Readiness

Lead preparation activities for internal audits and external regulatory inspections (FDA, EU, etc.).
Oversee audit response processes, ensuring timely, thorough closure of observations and CAPAs.
Maintain a continuous state of inspection readiness across the organization.

Cross-Functional Collaboration

Partner with Manufacturing, Validation, Regulatory Affairs, R&D, and other stakeholders to ensure effective integration of quality systems.
Provide quality oversight for:
- New product introductions (NPI)
- Technology transfers
- Process and system changes
Performs other duties as assigned by management

Department Specific/Non-Essential Functions:

Support site-specific initiatives related to digital QMS tools or system implementations.
Contribute to training program development for quality systems and compliance topics.
Participate in or lead continuous improvement or Operational Excellence (OpEx) projects outside core QMS ownership.
Provide support during regulatory submissions or inspections as a subject matter expert (SME), as needed.
Assist in benchmarking or industry best practice evaluations to enhance QMS maturity.
Support additional departmental projects or cross-site initiatives as assigned.
Performs other duties as assigned by management

YOUR BACKGROUND

Required Qualifications

Bachelor’s degree in Life Sciences, Engineering, or related field
7+ years of experience in pharmaceutical QA, with 3+ years in quality systems leadership.
Deep understanding of GMP regulations (21 CFR Parts 210/211, EU Annexes, ICH Q10).
Proven experience managing audits and regulatory inspections.
Strong analytical, organizational, and communication skills.

Preferred Qualifications

Advanced degree (MS, MBA, or Ph.D.).
Experience with electronic QMS platforms
Six Sigma or Lean certification
Experience in sterile manufacturing or biologics

Apply Now

Refine Your Search

analytical validation manager jobs in wake forest, nc

QA Systems Manager

Systems Analyst IV

Associate Dean, Financial Aid Technology, Reporting and Training

Senior Construction Performance Analyst

Quality Technical and Validation Manager

Manager, Clinical Labs - External Referral Lab

HR Manager

Manager, Payroll N.A.

Senior/Commercial Pricing and Contracting Manager, Market Access

Regulatory Compliance Lead

Senior Consultant - Clinical Documentation Specialist

Manager, Financial Crimes Oversight Testing U.S.

Technology Incubation – Early Stage Product Manager

MSAT Technical Lead – Drug Substance (Sr Manager)

Martech Developer- Manager

Business Development Associate - Pharmaceutical

ERP Data Management Lead

HR & Benefits Analyst

Marketing Engagement Associate Manager

Production Supervisor - 2nd Shift

I want to receive the latest job alert for analytical validation manager in wake forest, nc

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