Overview of the role
To carry out the repackaging and relabeling of pharmaceutical products imported via parallel trade, ensuring full compliance with Good Manufacturing Practice (GMP), regulatory standards, and company Standard Operating Procedures (SOPs). The operative will work in a cleanroom or controlled environment and play a key role in maintaining product quality and patient safety.
Main Responsibilities
Operate within a GMP-regulated environment, adhering to MHRA, EU, and company-specific quality standards.
Perform repackaging and relabeling of pharmaceutical products according to batch records and production instructions.
Ensure that all work is carried out with high levels of accuracy and attention to detail to prevent product mix-ups and labeling errors.
Follow SOPs and complete relevant documentation (e.g., batch manufacturing records) accurately and in real time.
Handle products in accordance with regulatory and internal guidelines to maintain product integrity.
Conduct line clearance, cleaning, and set-up activities for production areas and equipment.
Report any deviations or non-conformances to the Quality or Production Supervisor promptly.
Support internal audits and inspections by regulatory bodies or customers.
Assist with stock control and reconciliation of materials used in production processes.
Maintain cleanroom discipline and hygiene practices at all times.
Participate in continuous improvement initiatives to enhance production efficiency and quality compliance.
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