Trainee QP: QA Regulatory Manager (Sterile Pharma)

RBW Consulting; Manchester; Hybrid; GBP 40,000 - 65,000; Full time

Benefits offered by this job

Job summary

RBW Consulting is seeking a QA Regulatory Manager (Trainee / Newly Qualified QP) for site-based work with potential long-term remote flexibility. The role covers QA, Regulatory Affairs and QP-related activities across multiple UK sites, including Manchester, with career development and training opportunities.

You will support QP activities, regulatory projects and quality systems while developing expertise in sterile manufacturing and regulatory compliance in a dynamic environment.

Qualifications

• Progress toward QP eligibility or recently qualified as a QP.
• GMP-regulated pharmaceutical experience.
• Exposure to QA, Regulatory Affairs or Quality Systems activities.
• Understanding of UK/EU GMP requirements.
• Experience in sterile/aseptic manufacturing environments is a plus.
• Strong communication across functions.
• Science degree or equivalent qualification.

Responsibilities

• Support QP activities and batch certification processes.
• Assist with regulatory projects, licence maintenance, variations and submissions.
• Contribute to IMP and commercial product regulatory activities, including documentation.
• Support quality systems including deviations, CAPAs, change controls and risk assessments.
• Collaborate with Quality, Manufacturing, QC and Development to ensure GMP compliance.
• Assist with inspections, audits and interactions with regulatory authorities.
• Review and approve quality documentation including SOPs, protocols and reports.
• Develop knowledge in sterile manufacturing and aseptic processing.

Skills

QP eligibility

GMP experience

Regulatory affairs exposure

Quality systems

UK/EU GMP knowledge

Sterile manufacturing

Communication skills

Science degree

Education

Scientific degree or equivalent

Job description

RBW Consulting is seeking a QA Regulatory Manager (Trainee / Newly Qualified QP) for site-based work with potential long-term remote flexibility. The role covers QA, Regulatory Affairs and QP-related activities across multiple UK sites, including Manchester, with career development and training opportunities.

You will support QP activities, regulatory projects and quality systems while developing expertise in sterile manufacturing and regulatory compliance in a dynamic environment.