CQ Specialist DC PL

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.

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: 0–2 years of relevant work experience in quality, compliance, or regulated operations; basic knowledge of quality management systems (QMS) and regulated environments (e.g., medical devices, pharmaceuticals, or healthcare).
• Skills: 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 adherence to procedures.

Additional Requirements

• 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 required.

Benefits

• Base salary: zł163,000.00 – zł262,200.00.
• Annual bonus with set target (% of pay) based on performance.
• Vacation days, parental leave (minimum 12 weeks), bereavement leave, caregiver leave, volunteer leave.
• Well‑being reimbursement, programs for financial, physical and mental health.
• Service anniversary and recognition awards; eligible dependents can participate in several insurance plans.

Equal Opportunity Employer

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.