Open to opportunities

Aisha Robinson

@aisharobinson

Message

Quality and operations specialist delivering compliant GMP readiness through training consistently.

United States

Message

What I'm looking for

I’m looking to lead quality and compliance execution in a highly regulated environment—owning controlled documentation, investigations/CAPA, training strategy, and inspection readiness—while partnering cross-functionally to drive continuous improvement with strong data integrity.

I’m a quality and operations leader with 21+ years of experience across GMP-regulated pharmaceutical manufacturing, laboratories, and packaging operations. My focus is keeping work inspection-ready through strong documentation control, data integrity, and compliance management.

In my current role as a Principal Specialist, Operations & Packaging, I manage review and approval of GMP-controlled documents, ensuring accuracy and data integrity. I support deviation management, root-cause analysis, and CAPA execution, lead equipment/documentation change control, and partner with QA Engineering on validation and qualification activities—while implementing training and compliance strategies that strengthen audit readiness.

Previously, I served as a Compliance Manager and a Training Supervisor, where I developed and maintained compliance policies, SOPs, and curricula, executed internal audits, and tracked corrective actions and remediation. I also bring hands-on technical and systems depth from roles including Senior Chemist and LabWare LIMS SME experience, including method validation, QA-level data review, and global SME support during LIMS transition—always with a continuous improvement mindset in fast-paced, highly regulated environments.

Experience

Work history, roles, and key accomplishments

Current

Principal Specialist

Current

Boehringer Ingelheim Pharmaceuticals

Sep 2023 - Present (2 years 9 months)

Managed review and approval of GMP-controlled documents to ensure accuracy and data integrity. Supported deviation management, root-cause analysis, and CAPA execution, and performed change control for equipment and documentation to maintain audit readiness.

Deviation Management Root Cause Analysis CAPA Change Control Validation & Qualification Support Training & Audit Readiness

Compliance Manager

Winder Laboratories

Feb 2023 - Jul 2023 (5 months)

Developed and updated compliance policies, SOPs, and guidelines, and performed internal audits to identify compliance risks. Recommended corrective actions, tracked remediation, managed compliance documentation, and delivered compliance and ethics training across departments.

Compliance Management SOP Development Internal Audit Compliance Risk Management Ethics & Compliance Training

Training Supervisor

Jubilant Cadista Pharmaceuticals

Nov 2015 - Nov 2022 (7 years)

Developed and managed GMP documentation, including SOPs and training curricula, and supported investigations and CAPA documentation. Conducted cGMP training gap assessments, managed LMS reporting, and provided training for validation and system implementation with audit support.

SOP Development CAPA CGMP Gap Assessments Audit Support

Senior Chemist

Eurofins Lancaster Laboratories

Nov 2014 - Nov 2015 (1 year)

Performed method validations and analytical studies and completed QA-level data reviews. Supported investigations and delivered training on documentation standards and validation protocols.

data review Investigation Compliance Training

Associate Scientist

Teva Pharmaceuticals

Dec 2007 - Nov 2014 (6 years 11 months)

Reviewed analytical documentation and validation protocols to support audit readiness. Facilitated CAPA development and served as a global SME for LabWare LIMS during transition.

CAPA Audit Readiness Data Integrity