QA Compliance Coordinator China

For our Abbott Laboratories site in Zwolle, we are looking for a:

Are you detail‑oriented, quality‑driven, and excited about coordinating international regulatory and compliance projects? At Abbott in Zwolle, we are looking for a QA Compliance Coordinator China who ensures that our products, processes, and documentation meet all current Chinese regulatory requirements. You will play a key role in safeguarding quality, safety, and compliance across our global supply chain.

What will you do?

Documentation & Filing: * Act as Subject Matter Expert (SME) for China‑related QA documents (e.g., Change Procedure, China Recall Procedure, Drug Quality Manual). * Prepare and maintain China‑specific documentation (forms, templates, reports). * Update batch work orders in line with filing and registration requirements. * Ensure compliant document control (versioning, approvals, archiving) according to the site Quality Management System (QMS).

Regulatory Implementation * Review new or amended China regulations and summarize their impact for the Zwolle site. * Coordinate implementation projects (gap assessment → action plan → closure). * Contribute to China‑related regulatory training and deliver site training when needed. * Support evaluations and interpretations of China regulations.

Compliance Upgrades * Prepare and implement quality system documentation as part of our journey toward full China compliance. * Lead smaller project workstreams or support larger cross‑functional compliance projects. * Document and maintain the China drug policy and compliance roadmap for the Zwolle site. * Collaborate with Operations, QA/QC, Engineering, and other functions on GMP, food safety, and audit programs. * Support internal audits, host external audits/inspections, and follow up on CAPAs and management reporting.

JOB FAMILY: Regulatory Operations

DIVISION: ANSC Nutrition Supply Chain

LOCATION: Netherlands > Zwolle : Building 1

WORK SHIFT: Standard

TRAVEL: Not specified

MEDICAL SURVEILLANCE: No

SIGNIFICANT WORK ACTIVITIES: Keyboard use (greater or equal to 50% of the workday)

What do we offer? We offer a competitive salary. You will also receive an Individual Choice Budget (IKB) including holiday allowance, 13th month, special leave, and additional vacation days.

What do you bring? * Bachelor/HBO degree in Life Sciences, Food Technology, Chemistry, Microbiology, Pharmacy, or similar. * 1–3 years of experience in QA, Compliance, or Regulatory within a manufacturing environment (food, pharma, nutrition, or related). * Knowledge of quality systems and document control. * Understanding of regulatory pathways (change control, recall, filing) and eagerness to grow expertise. * Strong project coordination skills: planning, tracking, stakeholder follow‑up. * Fluent in English and Dutch; Mandarin is an advantage. * Proactive, detail‑oriented, and comfortable working cross‑functionally.