CQ Specialist DC PL

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Customer/Commercial Quality Job Category: People Leader All Job Posting Locations: Warsaw, Masovian, Poland Job Description: DePuy Synthes is recruiting for a CQ Specialist DC PL, located in Warsaw, Poland. Job Overview The CQ Specialist DC PL plays a key role in ensuring distribution center quality compliance for DePuy Synthes products in Poland. This position supports Quality & Regulatory Affairs (QARA) International by maintaining and improving quality processes, ensuring compliance with internal standards and external regulatory requirements, and supporting continuous improvement initiatives across distribution center operations. This role has direct impact on product quality, patient safety, and regulatory compliance, making it an exciting opportunity to contribute to the reliability and excellence of DePuy Synthes supply chain operations. Key Responsibilities Support and maintain quality processes related to distribution center (DC) operations, ensuring compliance with internal quality systems and applicable regulatory requirements. Execute and document quality assurance and compliance activities, including process monitoring, deviation handling, and corrective and preventive actions (CAPA). Prepare, maintain , and update quality documentation, including procedures, work instructions, records, and reports. Support internal audits, inspections, and assessments, including preparation of documentation and follow ‑ up on findings. Collaborate cross ‑ functionally with DC Operations, Supply Chain, and QARA partners to ensure consistent application of quality standards. Monitor and analyze quality data and trends to identify process improvement opportunities and support continuous improvement initiatives. Assist in the implementation of new or updated quality processes, systems, or regulatory requirements impacting DC activities. Qualifications Education Bachelor’s degree required in Quality, Engineering, Life Sciences, Pharmacy, or a related field. Advanced degree or quality ‑ related certification preferred. Experience and Skills Required: Typically 0–2 years of relevant work experience in quality, compliance, or regulated operations, aligned with entry ‑ level Quality professional roles. Basic knowledge of quality management systems (QMS) and regulated environments (e.g., medical devices, pharmaceuticals, or healthcare). Experience with documentation control, data review, and record management. Ability to work collaboratively in cross ‑ functional , international teams. Preferred: Experience supporting distribution center or supply chain quality activities. Familiarity with GxP , ISO, or medical device quality standards. Exposure to process improvement methodologies (Lean, Six Sigma, Kaizen). Experience preparing for or supporting audits and inspections. Strong attention to detail and ability to follow defined procedures and standards. Other: Language: Proficiency in English and Polish required for documentation and stakeholder communication. Travel: Limited travel may be required (up to ~10%), primarily regional or within Europe. Certifications: Quality certifications (e.g., ISO, Six Sigma Yellow/Green Belt) preferred but not r