QC Lab Analyst

💼 Job Title
QC Lab Officer

🔝 Reports to
QC Supervisor / QC Manager

🌐 Location
Aïn Ouda, Morocco

🏢 Work Mode
On-Site

🧭 Division
Quality

🗂️ Department
Quality Control – Laboratory

📝 Employment Type
Full-Time, Permanent

🧬 Why Cipla?
At Cipla, Caring for Life isn’t just our purpose – it’s our promise. We’re here to Make Life Thrive by making quality healthcare more accessible, inclusive, and impactful across the continent.
With innovation at our core and compassion in every decision, we’re building teams that challenge conventions, uplift communities, and shape the future of healthcare.
Whether you’re in labs, logistics, leadership, or on the factory floor – every role fuels our mission.
At Cipla, you grow with purpose, lead with empathy, and belong from day one.

🎯 Job Purpose
The content and statements in this job description are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the QC Lab Officer.
This job description is not intended to provide an exhaustive list of all tasks. Duties may be modified depending on department, group, or individual assignment. Education, training, and experience may also impact the role’s scope.

📌 Duties & Responsibilities
The general duties and responsibilities include but are not limited to:
• Perform sample management for all incoming raw materials, in-process, finished products, and stability samples (receipt, logging, distribution, destruction).
• Coordinate chemical and reference standard inventory; verify expired items and discard per procedures.
• Update and maintain sample information as per company requirements.
• Complete data entry and maintain lab records.
• Ensure lab consumables are available and place orders when required.
• Oversee temperature and humidity monitoring for stability chambers.
• Conduct sample loading in stability chambers and submit stability samples as per schedule.
• Assist in shipment of samples to contract labs as required.
• Provide general housekeeping in the QC lab and support other functional activities.
• Perform other duties as assigned by management.

🧾 Education & Experience
• Minimum: High School Diploma or equivalent.
• Preferred: Associate degree or higher in Chemistry, Laboratory Science, or related field.
• 2–4 years’ experience in the pharmaceutical industry (QC or lab setting).
• Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint) and lab-related systems.
• Fluency in French (mandatory) and English (preferred).
• Strong organizational, learning, and teamwork skills.
• Ability to analyze complex data sets.

🌟 Professional & Behavioural Competencies
• Must be willing to work in a pharmaceutical cGMP setting.
• Must be available for any assigned shift (Day, Evening, Night) and flexible for occasional weekend work.
• Positive and professional attitude with a collaborative mindset.
• No remote work available.

⚙️ Working Conditions
• Work is performed in a cGMP laboratory or manufacturing environment.
• Use of PPE required: uniforms, lab coats, safety glasses, respiratory protection, hearing protection, etc.
• Exposure to solvents, powders, or other pharmaceutical materials.
• Role may involve shift work (Day, Evening, Night).
• Physical demands: long periods of standing/walking, ability to climb ladders, and lifting up to 16 kg.

🎁 Employee Benefits & Perks

From wellness days and hybrid learning to Cipla University and real mentorship, we don’t just care for life – we power up your growth while we’re at it.

🌍 Learning & Upskilling Pathways
🧭 Mentorship & Career Growth
🧘 Wellness First: Mental health, mindfulness & more
🎂 Full-Day Birthday Leave
🏅 Recognition & Great Place to Work Vibes
🌱 Green Office Spaces Built for Well-being