Pharmaceutical Lab Scientist
Available for New Opportunities

Precision in
Pharma Quality

Ensuring safety, efficacy, and compliance through rigorous Quality Control and biotechnology innovation.

Sidahmed Bouchenak
About Me

Driving Quality &
Innovation in Pharma

A dedicated Quality Control Manager and Biotechnology expert with over a decade of experience in world-class pharmaceutical environments.

My professional journey represents a steadfast commitment to patient safety and product excellence. From leading validation protocols at GSK to managing complex QC operations for formulations like Eye Drops, I integrate rigorous scientific standards with strategic operational efficiency.

I specialize in bridging the gap between strict regulatory compliance (cGMP, ICH) and dynamic R&D innovation.

Master's in Biotech & QC
10+ Years Pharma Exp
cGMP, GLP & ISO 17025
Lean Six Sigma Green Belt
Sidahmed Bouchenak QC Manager & Biotech Master

Core Expertise

QC Management

QC Management

Ensuring product excellence through rigorous testing and compliance oversight. Managing lab operations efficiently.

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Method Validation

Method Validation

Developing and validating analytical methods compliant with ICH guidelines. Precision and accuracy guaranteed.

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Compliance Auditing

Compliance & GxP

Steering operations through complex regulatory landscapes including cGMP, GLP, and ISO 17025 audits.

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R&D Formulation

R&D Formulation

Innovation in liquid and eye drop formulations. Bridging the gap between concept and commercial scale-up.

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Competencies

Technical Toolkit

Advanced proficiency in analytical instruments, software, and regulatory standards.

Analytical Techniques

HPLC (Waters, Agilent) UV-Vis Spectrophotometry Dissolution Testing Karl Fischer IR Spectroscopy

Software & Data

LIMS Administration Empower 3 Minitab Python (Data Analysis) Microsoft Office Suite
Career

Professional Journey

Present

QC Manager

GenericLab

Leadership in QC operations, ensuring compliance and driving operational excellence across all dosage forms. Implementing new quality workflows.

Previous

R&D Manager

PharmAlliance

Spearheaded research initiatives for novel formulations, managing the full lifecycle from bench to pilot scale-up and validation.

Previous

QA Responsible

AFROPHARM

Managed QA processes, validation protocols, and regulatory documentation. Oversaw batch release procedures.

Previous

QC & Analytical Validation

GlaxoSmithKline (GSK)

Specialized in analytical validation and adherence to global pharmaceutical standards at one of the world's leading companies.

Background

Education

Master's Degree in Biotechnology

USTHB - University of Science and Technology

Snr Technician in Computer Science

Institute of Computer Science

Communications

Languages

ArabicNative
FrenchFluent
EnglishAdvanced

Resources & Downloads

Analytical Method Validation Protocol (ICH Q2)

PDF • 850 KB

Stability Study Planner Template

XLSX • 1.2 MB

These documents are for demonstration purposes.

Get in Touch

Open for opportunities in Quality Control management and consultancy.