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indy_singh16

Indy Singh

@indy_singh16

QC and Compliance Manager

Großbritannien
Englisch
Einige Informationen werden in englischer Sprache angezeigt.
Über mich
I help early-stage biotech and pharma startups build audit-ready GMP documentation systems and cleanroom compliance frameworks. With hands-on experience in GMP production, QC, and stability testing across UK and international biopharma, I understand regulatory expectations. I design structured SOP hierarchies, document control systems, and compliance checklists that reduce risk and support scalable growth.... Mehr lesen

Kompetenzen

i
indy_singh16
Indy Singh
offline • 
Durchschnittliche Antwortzeit: 1 Stunde

Meine Dienstleistungen

Zertifizierungen und Vorschriften
I will structure gmp documentation and cleanroom compliance system
Risikomanagement
I will prepare ukca and ce compliance documents

Portfolio

Arbeitserfahrung

Smile_Therapy

Compliance Manager

Smile Therapy • Vollzeit

Dec 2025 - Present9 mos

Ensure product conformity with UKCA/CE marking, WEEE, REACH, and applicable safety directives Review and validate technical documentation including Declarations of Conformity, risk assessments, and laboratory test reports Manage supplier compliance verification and quality documentation audits Implement structured document control systems aligned with regulatory best practices Oversee batch verification and pre-shipment inspection protocols Liaise with third-party conformity assessment bodies and external regulatory advisors Develop corrective and preventive action (CAPA) processes for non-conforming products Conduct regulatory risk assessments prior to product launch Monitor changes in UK and international product safety legislation

Quality & Compliance Officer

Medik8 • Vollzeit

Dec 2024 - Dec 20251 yr

Led GMP-compliant production operations within a controlled cleanroom environment, ensuring documentation accuracy, in-process quality control, and regulatory alignment. • Strengthened document control practices to improve compliance readiness • Conducted in-process quality checks aligned with GMP standards • Identified workflow inefficiencies and proposed process improvements • Maintained batch records and ensured traceable documentation • Supported cross-functional teams in maintaining audit-aligned production systems