Quality Engineer

We are working with a high growth pharmaceutical manufacturer who are working on an exciting expansion project and are currently looking at making some integral contract hires for a long term project with the possibility of this turning into a permanent role.

The successful candidate will be responsible for supporting all aspects of the quality system within the manufacturing facility. This includes supporting quality control, inspections of raw and in process material, finished product testing, documentation review, and maintaining batch records with compliance to good manufacturing practices

Responsibilities

• Visually inspect quarantined materials and in-process products
• Review certificates of analysis (CoA) and analytical laboratory report
• Review Batch Production Records for accuracy and completeness
• Write, review, and approve documents in the quality management system
• Conduct continuous improvement processes including root cause analysis, improvement projects, development of new documents, and training of staff
• Participate in internal and external audits

Qualifications

• Associate's degree in a relevant field, such as life sciences, industrial engineering; or equivalent professional experience
• 2 years of experience in the pharmaceutical industry preferred
• Strong understanding of GMP
• Excellent written and verbal communication skills
• Ability to work independently and as part of a team
• Ability to think critically and solve problems

Please get in touch on h.stainton@hamlynwilliams.com or apply directly.