Analytical Development and Compliance Supervisor

We are seeking an Analytical Development & Compliance Supervisor to

lead our Analytical Development and Stability teams, ensuring new

product development and routine testing meet regulatory, GMP, and cGMP

standards. You will manage method development, validation, stability

testing, compliance, and documentation, while fostering a high performing,

engaged team.

What you will do:

Lead and mentor Analytical Development and Stability teams, managing workflow, performance, training, and succession planning.

Oversee method development, validation, stability testing, and transfer of analytical methods to QC.

Ensure GMP, GLP, and regulatory compliance in all laboratory activities.

Maintain data integrity, documentation, SOPs, and audit readiness (SAHPRA, ISO, other regulatory audits).

Support budgeting, cost control, resource allocation, and continuous improvement initiatives.

Collaborate with Production, QC, RA, QA, and external partners to ensure accurate, timely testing and reporting.

Why join Nautilus Pharma?

Contribute to products that make a real impact on health and wellbeing.

Grow professionally with visible leadership support and opportunities for continuous learning.