GxP Compliance & Quality Systems Coordinator

Biopharma Careers

Gebze

On-site

TRY 350,000 - 520,000

Full time

14 days+
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Biopharma Careers is seeking a Quality/QA professional in Gebze to ensure GxP compliance and scalable quality systems across site activities. You will coordinate audits, CAPA and supplier oversight while supporting change control and documentation management.

Experience in pharma/biotech QA, environmental monitoring, and regulatory liaison is essential for success in this role and for ensuring timely responses to inspections and HA communications.

Qualifications

  • QC/QA experience in pharmaceutical ind./biotech with environmental monitoring and clean zones.
  • Experience implementing GMP/GxP compliance and quality systems.
  • Audit, CAPA and inspections experience.

Responsibilities

  • Support all compliance activities including SQM, PQR, DMS, CHANGE, training, archiving, audits, recall etc.
  • Implementation of Quality Systems (incl. documentation management)
  • Supplier management activities (agreements, oversight, audit)
  • Preparation/support and coordination of CAPA/follow-up
  • Audit and inspection preparation and support
  • Change control review/approval -Ensure local DI and eCompliance oversight (training, inspections, plan, risk ID etc.)
  • Ensure process quality assurance acc. to regulations
  • QP declaration review and approval -KPI trending
  • Ensure applications, certificate maintenance etc. to local HA
  • SPOC for communication with HA, GCA / One voice / consolidated approach / synergies for all sites within same HA jurisdiction / country
  • Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt
  • Distribution of marketing samples (where applicable)

Skills

Action Oriented
Continuous Learning
Dealing With Ambiguity
Gmp Procedures
Process Optimization
QA (Quality Assurance)
Quality Standards
Self-Awareness
Technological Expertise
Technological Intelligence
GxP
Industry standards
Compliance requirements

Job description

Biopharma Careers is seeking a Quality/QA professional in Gebze to ensure GxP compliance and scalable quality systems across site activities. You will coordinate audits, CAPA and supplier oversight while supporting change control and documentation management.

Experience in pharma/biotech QA, environmental monitoring, and regulatory liaison is essential for success in this role and for ensuring timely responses to inspections and HA communications.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

GxP Quality Compliance Specialist
GxP Quality Compliance Specialist

TR11 (FCRS = TR011) Sandoz Grup Sağlık Ürünleri İlaçları Sanayi ve Ticaret A.Ş. • Gebze

On-site
TRY 60,000 - 80,000
QC Analyst – cGxP, Stability & Micro QC
QC Analyst – cGxP, Stability & Micro QC

Sandoz • Gebze

On-site
TRY 180,000 - 320,000
Quality Systems Specialist: Elevate GMP & QA Impact
Quality Systems Specialist: Elevate GMP & QA Impact

Recordati • Çerkezköy

On-site
TRY 300,000 - 420,000
Quality Systems Specialist
Quality Systems Specialist

Recordati • Çerkezköy

On-site
TRY 300,000 - 420,000
Food Safety QA & Compliance Specialist
Food Safety QA & Compliance Specialist

Sensient Technologies Corporation • Gebze

On-site
TRY 240,000 - 300,000
Onsite 5 days a week
Competitive salary and benefits
Comprehensive onboarding and training
Regulatory and Quality Manager
Regulatory and Quality Manager

Ferring Holding SA • Turkey

On-site
TRY 80,000 - 100,000
Quality Compliance Coordinator (Temp.)
Quality Compliance Coordinator (Temp.)

Biopharma Careers • Gebze

On-site
TRY 350,000 - 520,000
Quality Operations Leader - CAPA, Audits & Analytics
Quality Operations Leader - CAPA, Audits & Analytics

Pfizer • Fatih

Hybrid
TRY 180,000 - 300,000
Hybrid work model
Global exposure
Pharma QC Analyst — Mastering GMP Analytics
Pharma QC Analyst — Mastering GMP Analytics

TR11 (FCRS = TR011) Sandoz Grup Sağlık Ürünleri İlaçları Sanayi ve Ticaret A.Ş. • Gebze

On-site
TRY 30,000 - 50,000
Kalite Uzmanı
Kalite Uzmanı

Randstad Türkiye • Çankaya

On-site
TRY 180,000 - 240,000