Quality Assurance Specialist II

Scientific Search; Charleston (SC); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

100% company-paid medical, dental, and vision coverage

401(k) with employer match up to 4%

Company-paid disability and life insurance

Gym reimbursement and PTO

Job summary

Scientific Search in the Greater Charleston, SC Area is looking for a Quality Manager to lead supplier qualification and quality assurance processes. The ideal candidate should have a Bachelor's degree and experience in a cGMP manufacturing environment. You will manage quality issues, conduct internal audits, and support complaint investigations.

The role offers competitive compensation and comprehensive benefits, including full medical coverage and career growth opportunities. Interested candidates can apply by emailing [e-mail] with Job#19955.

Qualifications

• Bachelor’s degree required.
• Experience in a cGMP manufacturing environment.
• Strong knowledge of quality systems, audits, CAPA, and supplier quality management.

Responsibilities

• Lead supplier qualification processes and audits.
• Manage supplier quality issues and investigations.
• Conduct internal audits and Product Quality Reviews.
• Support complaint investigations and adverse events activities.
• Review SOPs and quality system documentation.

Skills

cGMP manufacturing experience

Quality systems knowledge

Audit experience

CAPA management

Cross-functional project leadership

Education

Bachelor’s degree

Job description

Location: Greater Charleston, SC Area

Why You Should Apply

• Competitive compensation
• 100% company-paid medical, dental, and vision coverage
• 401(k) with employer match up to 4%
• Company-paid disability and life insurance
• Gym reimbursement, supplement allowance, PTO, holidays, and volunteer time
• Professional development and career growth opportunities

What You’ll Be Doing

• Lead supplier qualification, auditing, and quality agreement processes
• Manage supplier quality issues, investigations, CAPAs, and resolutions
• Conduct internal audits, mock recalls, and Product Quality Reviews
• Support complaint investigations, adverse events, and stability programs
• Review SOPs, change controls, and quality system documentation

About You

• Bachelor’s degree required
• Experience in a cGMP manufacturing environment
• Strong knowledge of quality systems, audits, CAPA, and supplier quality management
• Ability to lead cross-functional projects and influence stakeholders
• Comfortable traveling up to 10% for supplier audits and quality activities

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to [e-mail] and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19955.