Temp. position- Quality Engineer- Pharma industry

We are looking for a Quality Assurance Engineer to join our Quality team for a temporary position of approximately 8 months, with a possibility of extension based on business needs. This is a varied and hands-on role within a manufacturing environment.

Working Hours:

• Full-time: 07:00–16:00
• Alternative option (parent-friendly position): 08:00–16:00
• Willingness to work overtime when required

Key Responsibilities:

• Act as a Quality Assurance Engineer as part of the site Quality team, supporting plant-level quality activities
• Support plant preparation for regulatory inspections, customer audits, and certification audits, including responses to audit findings
• Handle deviations, non-conformance reports, and customer complaints
• Review and release manufacturing batches
• Manage change control processes, including preparation of summaries, identification of documents for update, and follow-up on implementation and effectiveness
• Write and update SOPs, work instructions, protocols, and quality-related reports
• Participate in internal and external quality audits (including suppliers and printing houses)
• Review incoming raw material documentation and support supplier management
• Prepare Annual Product Reviews (APR)
• Handle customer quality requirements such as quality questionnaires, declarations, and change requests

Job Requirements:

• Bachelor’s degree in chemical engineering, Biotechnology Engineering, or Mechanical Engineering
• Previous experience in a pharmaceutical manufacturing environment working under GMP – required
• Experience with quality systems/software, ERP systems, and Office applications – an advantage
• Proficiency in Microsoft Office – required
• Immediate availability