QA & QC Oversight Specialist - GMP Biotech/Pharma

Eurofins; Sanford (NC); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Medical coverage

Dental & vision

401(k) with match

Paid vacation and holidays

Life and disability insurance

Job summary

Eurofins PSS Insourcing Solutions is seeking a Quality Assurance professional to provide QA oversight of QC activities within a biotech/pharmaceutical manufacturing environment. The role includes QA review and approval of QC method validation, equipment qualification, protocols, reports, and process control documents.

Ideal candidate will have 4+ years in manufacturing, laboratory, quality, or engineering within biotech/pharma, GMP experience, and hands-on experience with method validation,

Qualifications

• BS or BA in science or related field, with minimum 4 years of experience in biotech/pharmaceutical manufacturing, lab, quality, or engineering.

Responsibilities

• QA oversight of QC activities and assurance of quality systems.
• QA review/approval of QC method validation, equipment qualification, protocols, reports and related documents.
• Support evaluation and resolution of QC deviations/investigations and drive process improvements.

Education

BS or BA in science or related field

Tools

Method Transfer Validation

Investigation

Change Controls

Equipment Qualification

HPLC

GC

Raw materials testing

Job description

Eurofins PSS Insourcing Solutions is seeking a Quality Assurance professional to provide QA oversight of QC activities within a biotech/pharmaceutical manufacturing environment. The role includes QA review and approval of QC method validation, equipment qualification, protocols, reports, and process control documents.

Ideal candidate will have 4+ years in manufacturing, laboratory, quality, or engineering within biotech/pharma, GMP experience, and hands-on experience with method validation,