GCP QA Auditor

ZigZag QA

Brasil

Remote

BRL 458,000 - 611,000

Full time

14 days+

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Flexible working schedule
Competitive compensation package
Sustainability policy
Global exposure

Job summary

ZigZagQA, a global QA leadership firm, seeks a Senior GCP QA Auditor for a permanent remote role across South America. You will audit Investigator Sites and Vendors, including eTMF audits, and support Inspection Readiness and Inspection Management for diverse clients.

Expect 70% utilisation with up to 50% travel to client sites. The role emphasizes quality delivery, client focus, and collaboration with leading pharma and biotech teams.

Qualifications

  • Extensive auditing experience in GCP.
  • Thorough knowledge of GCP requirements.
  • Knowledge of other GxP areas (GLP, GCLP, GMP, CSV, PV) is advantageous.
  • Able to audit Investigator Sites with limited oversight.
  • Life science degree required.
  • Strong client focus.

Responsibilities

  • Audit Investigator Sites and Vendors, including eTMF audits, remotely.
  • Support Inspection Readiness and Inspection Management activities across regulatory bodies.
  • Manage assignments with a focus on timely delivery and client satisfaction.

Skills

GCP auditing
GCP knowledge
GxP familiarity
Investigator audits
Client focus

Education

Life science degree

Job description

GCP QA Auditor – Full Time – Permanent – Remote – South America

Are you experienced in Good Clinical Practice? Do you have extensive auditing experience?

We are currently recruiting for a Senior GCP QA Auditor to join us at Zigzag on a permanent basis. You will become a pivotal member of our team, working alongside industry leading experts and delivering our client’s quality assurance aspirations and outcomes.

What we are looking for
  • Extensive auditing experience in GCP.
  • Thorough knowledge of GCP.
  • Additional knowledge of another GxP areas (GLP, GCLP, GMP, CSV, PV) would be advantageous.
  • Able to confidently audit Investigator Sites with limited oversight.
  • Life science degree.
  • Strong client focus.
What Zigzag has to offer you
  • Leading Quality Assurance consultancy company – Our auditors work internationally across different types of organizations and audits and other QA related projects, with top thought-leaders in the industry.
  • We are committed to continuous professional development.
  • Fostering Success in our Auditors - Scheduling to ensure you are able to deliver your best, every time.
  • A Truly Supportive and Management Team – Having a supportive and open leadership team allows our people to show up and be their best.
  • WiZe working schedule - Flexible working schedule to allow you to live your life around work.
  • A Competitive Compensation Package – We believe our people need to be compensated for their dedication.
  • Sustainability – We endeavour to keep auditors travel as local as possible to reduce our carbon footprint in line with our sustainability policy as well as ensuring you have a work/life balance.
What You’ll Do With Us

Auditors target will be to work to 70% utilisation, which could require up to 50% travel to client sites, that doesn’t mean you’ll be away from home for months at a time, as we ensure we schedule assignments for a fair work/life balance.

Our auditors are deployed to audit Investigator Sites and Vendors, as well as eTMF audits which are done remotely.

You’ll support our clients with Inspection Readiness and Inspection Management related activities across a diverse range of roles and regulatory bodies.

Who We Are

ZigZagQA is a trusted global leader in QA management, offering true global reach and unrivalled expertise to reduce risk and efforts. Working as an extension of our clients team, our experts increase capability and efficiency with collaborative, comprehensive and customized QA programs.

We partners with a wide range of clients across the entire drug discovery and development process to improve GxP Quality against global regulatory standards. We work with top 20 Pharmaceutical and Biotechnology companies, all the way to startups.

We strive for excellence, aiming to be the number one choice for our clients and our employees. We are passionate about Continuous Improvement and are always looking for a ‘better way’. We are a global, quality leader who put people first and forge lasting relationships to bring deep impact in the industry.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Freelance GCP Auditor
Freelance GCP Auditor

Barrington James • Brazil

On-site
BRL 120,000 - 240,000
Pharmaceutical Quality GMP Auditor (Consulting)
Pharmaceutical Quality GMP Auditor (Consulting)

Advarra • Brazil

Hybrid
BRL 455,000 - 834,000
GCP Auditor – Porto Alegre, Brazil (Ad hoc)
GCP Auditor – Porto Alegre, Brazil (Ad hoc)

Planet Pharma • Porto Alegre

On-site
BRL 221,000 - 332,000
Regional Clinical Quality Associate Director - São Paulo/Brazil
Regional Clinical Quality Associate Director - São Paulo/Brazil

AstraZeneca • Cotia

On-site
BRL 300,000 - 550,000
Clinical Fsp Quality Manager
Clinical Fsp Quality Manager

IQVIA Inc • São Paulo

On-site
BRL 260,000 - 380,000
Senior Global Trial Manager
Senior Global Trial Manager

IQVIA • São Paulo

Remote
BRL 601,000 - 820,000
CRA 2
CRA 2

IQVIA • São Paulo

On-site
BRL 120,000 - 180,000
CRA 1
CRA 1

BZL IQVIA RDS Brasil Ltda • São Paulo

On-site
BRL 120,000 - 180,000
Engenheiro de QA de Software - Trabalho Remoto
Engenheiro de QA de Software - Trabalho Remoto

BairesDev • São Paulo

Remote
BRL 312,000 - 520,000
100% remote work
Excellent compensation
Flexible hours
+2
Quality Analyst - Brazil
Quality Analyst - Brazil

GEP • São Paulo

Hybrid
BRL 90,000 - 150,000