QA Master Data Specialist - 12-Month Contract

Biopharma Asia; Latina; Hybrid; EUR 30,000 - 49,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Well-being reimbursement

Recognition programs

Job summary

Johnson & Johnson is seeking a Quality Assurance Associate – Master Data in Latina, Italy. You will ensure Master Data quality, approve production documents, and support GMP-compliant processes across the site.

The role demands a Master’s degree in a relevant field, 12 months pharma experience, and strong English and Office skills. MES/PAS-X and SAP knowledge are a plus. 12-month fixed-term contract.

Qualifications

• Master's degree or equivalent in a relevant field (Chemistry, Pharmacy, Bio, Eng, CompSci).
• 12 months of experience in pharma or similar.
• Excellent English language skills.
• Good knowledge of MS Office package.
• MES systems knowledge, preferably PAS-X, and SAP is a plus.

Responsibilities

• Approve production documentation (Master Batch Records) and master data for materials, equipment and resources, ensuring on-time and quality.
• Monitor cycle time and coordinate with global group for Master Data approvals.
• Control and ensure data quality for Master Data per GMP requirements.
• Collaborate with cross-functional project teams (NPI, Tech Transfer, Technical Launch, Validation Process) to ensure product launches.
• Support quality processes including handling non-conformities, CAPAs and Change Controls.
• Resolve plant-level issues related to products, processes, equipment, facilities and utilities to ensure quality and safety.
• Act as QA representative in company projects to uphold quality aspects.
• Serve as SME for Data Integrity to ensure proper data governance and system capabilities.
• Ensure GMP document approvals for IT systems and equipment; ensure validated systems and proper documentation.
• Provide QA support to Production for critical situations.

Skills

Accountability

Administrative Support

Compliance Management

Detail-Oriented

Document Management

Execution Focus

Goal Attainment

Human-Centered Design

Internal Controls

Process Oriented

Quality Control (QC)

Quality Management Systems (QMS)

Quality Standards

Report Writing

Education

Master's degree in Pharmaceutical Chemistry/Technologies, Pharmacy, Chemistry, Biology, Engineering, Computer Science

Job description

Johnson & Johnson is seeking a Quality Assurance Associate – Master Data in Latina, Italy. You will ensure Master Data quality, approve production documents, and support GMP-compliant processes across the site.

The role demands a Master’s degree in a relevant field, 12 months pharma experience, and strong English and Office skills. MES/PAS-X and SAP knowledge are a plus. 12-month fixed-term contract.