QA Associate: Real-Time Quality in Pharma Manufacturing

Mindlance; Winchester; On-site; GBP 35,000 - 45,000; Full time

Job summary

A pharmaceutical company is seeking a QA Associate in Winchester to oversee quality support functions in manufacturing solid oral dosage products. Responsibilities include ensuring compliance with cGMP, reviewing batch records, performing real-time audits, and assisting in investigations for deviations. The ideal candidate will possess a Bachelor's Degree in a scientific field or a High School Diploma with extensive experience in a regulated GMP environment. Strong communication and documentation skills are essential for this role.

Qualifications

• Bachelor’s Degree in a related field and 2 years of relevant experience preferred.
• Minimum 4 years experience in regulated GMP manufacturing required.

Responsibilities

• Oversee manufacturing operations through document review and approval.
• Perform real-time audits of batch records for compliance.
• Monitor production areas for adherence to safety and quality requirements.
• Assist in investigations for product deviations.

Skills

Good communication skills

Basic math and computer skills

Safe work habits

Excellent documentation and handwriting skills

Sound decision-making, technical and problem-solving skills

Time management skills

Familiarity with basic laboratory instrumentation

Proficient reading and comprehension skills

Demonstrates initiative

Education

Bachelor’s Degree in related science or technical field

High School Diploma with 4+ years relevant work experience

Job description

A pharmaceutical company is seeking a QA Associate in Winchester to oversee quality support functions in manufacturing solid oral dosage products. Responsibilities include ensuring compliance with cGMP, reviewing batch records, performing real-time audits, and assisting in investigations for deviations. The ideal candidate will possess a Bachelor's Degree in a scientific field or a High School Diploma with extensive experience in a regulated GMP environment. Strong communication and documentation skills are essential for this role.