Pharma Production Technician – GMP & Lean Improvement

GlaxoSmithKline plc; Burgos; On-site; EUR 38,000 - 64,000; Full time

Job summary

GSK on-site in Spain seeks a hands-on OSD production specialist to support manufacturing of oral solid dosage products. You will collaborate with operators, engineers and quality colleagues to keep production lines safe, compliant and efficient.

You will contribute to continuous improvement, support GMP compliance and assist in deviation investigations, CAPA and root cause analysis with cross-functional teams. A background in SAP/electronic batch records is a plus.

Qualifications

• University degree or vocational qualification in engineering, pharmacy, chemistry or a related technical field.
• At least 2 years’ experience in a pharmaceutical or regulated manufacturing environment.
• Practical knowledge of GMP and quality practices in pharmaceutical industry.
• Experience working on oral solid dosage packaging lines.
• Basic user skills in production systems such as SAP or electronic batch records.

Responsibilities

• Operate and monitor OSD packaging lines (Blister and Bottle) to meet production plans, safety and quality targets.
• Investigate deviations, support root cause analysis, and help implement corrective and preventive actions.
• Follow, maintain and suggest improvements to Standard Operating Procedures and work instructions.
• Support internal and external audits and help maintain compliance with Good Manufacturing Practice (GMP).
• Record production data accurately and use SAP or local systems for transactions and reporting.
• Contribute to continuous improvement projects using practical problem solving and production data.

Skills

GMP knowledge

OSD packaging experience

Attention to detail

Education

University degree or vocational qualification in engineering, pharmacy, chemistry or related technical field

Tools

SAP

Electronic batch records

Job description

GSK on-site in Spain seeks a hands-on OSD production specialist to support manufacturing of oral solid dosage products. You will collaborate with operators, engineers and quality colleagues to keep production lines safe, compliant and efficient.

You will contribute to continuous improvement, support GMP compliance and assist in deviation investigations, CAPA and root cause analysis with cross-functional teams. A background in SAP/electronic batch records is a plus.