Senior Quality Assurance Specialist

RBW Consulting; Greensboro (NC); On-site; USD 80,000 - 100,000; Full time

Job summary

RBW Consulting is seeking a Quality Assurance Supervisor for a rapidly growing CDMO in Winston-Salem. The role involves supervising QA operations, leading a team, and ensuring compliance with industry regulations. Ideal candidates have a strong background in quality assurance within the biopharma sector and are ready to contribute in a dynamic environment.

Benefits

Competitive salary and benefits package

Dynamic and mission-driven team environment

Opportunity for growth with an expanding organization

Qualifications

• 5+ years of experience in Quality Assurance within pharmaceutical, biotech, or CDMO environments.
• Strong knowledge of cGMP, ICH, and FDA regulations.
• Prior supervisory or team lead experience preferred.

Responsibilities

• Supervise day-to-day QA operations, including batch record review and deviation investigations.
• Lead and mentor QA Associates and Specialists.
• Collaborate with Manufacturing, QC, and Development teams.

Skills

Communication

Organizational Skills

Leadership

Education

Bachelor’s degree in Life Sciences, Chemistry, or related field

Job description

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This range is provided by RBW Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$80,000.00/yr - $100,000.00/yr

Direct message the job poster from RBW Consulting

Providing expertise to CMO/CDMO partners across the US

Job Title: QA Supervisor

Location: Winston-Salem, NC

Industry: Biopharmaceuticals / Contract Development and Manufacturing

Employment Type: Full-Time

Overview:

A rapidly growing contract development and manufacturing organization (CDMO) in Winston-Salem is seeking a Quality Assurance Supervisor to support its continued success in the biopharma sector. With a strong track record in pharmaceutical development and recent expansions in biologics and sterile manufacturing, this organization is at the forefront of delivering innovative solutions for clients across the life sciences industry.

Key Responsibilities:

• Supervise day-to-day QA operations, including batch record review, deviation investigations, and change control oversight.
• Lead and mentor QA Associates and Specialists, ensuring alignment with cGMP and FDA regulations.
• Collaborate closely with Manufacturing, QC, and Development teams to ensure product quality across all phases of development and production.
• Support client audits and regulatory inspections, contributing to audit readiness and compliance culture.
• Drive continuous improvement in QA systems, procedures, and documentation practices.

Qualifications:

• Bachelor’s degree in Life Sciences, Chemistry, or related field.
• 5+ years of experience in Quality Assurance within pharmaceutical, biotech, or CDMO environments.
• Strong knowledge of cGMP, ICH, and FDA regulations.
• Prior supervisory or team lead experience preferred.
• Excellent communication and organizational skills, with the ability to work in a fast-paced, collaborative environment.

What We Offer:

• Opportunity to grow with an expanding organization recognized for its leadership in biopharma development and sterile manufacturing.
• Dynamic and mission-driven team environment.
• Competitive salary and benefits package.
• The chance to contribute to cutting-edge development programs that make a real difference in patient care.

Join a company shaping the future of biologics and pharmaceutical development in the Southeast. Apply today to advance your career in quality and compliance.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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