Job Summary
* Company: Zenotech Laboratories
* Position: Quality Assurance and Quality Control (QA/QC)
* Employment Type: Full-time
* Industry: Pharmaceutical Manufacturing
* Role Focus: Ensuring compliance, product integrity, and adherence to regulatory standards
* Location: Pharmaceutical Manufacturing Facilities
Job Overview
Zenotech Laboratories is currently seeking dedicated, detail-oriented, and highly skilled professionals to join our Quality Assurance (QA) and Quality Control (QC) departments. We are committed to maintaining the highest standards of pharmaceutical excellence and are looking for individuals who share our passion for precision and patient safety.
As a member of our QA/QC team, you will play a vital role in our production ecosystem, ensuring that every product leaving our facility meets strict internal quality benchmarks as well as global regulatory requirements. Whether you are an experienced professional looking to advance your career or a talented individual eager to make an impact in the pharmaceutical sector, we invite you to explore this opportunity with our growing team.
Key Responsibilities
Quality Assurance (QA) Department:
* Manage and maintain the Quality Management System (QMS), including document control, change controls, deviations, and Corrective and Preventive Actions (CAPA).
* Conduct regular internal audits to ensure compliance with Current Good Manufacturing Practices (cGMP) and internal standard operating procedures (SOPs).
* Review batch manufacturing records (BMR) and batch packaging records (BPR) to ensure accuracy and completeness before final product release.
* Oversee vendor qualification processes and perform assessments to ensure the quality of raw materials and service providers.
* Act as a point of contact for regulatory inspections and support external audits.
* Assist in risk management activities to identify and mitigate potential quality issues during production.
Quality Control (QC) Department:
* Perform routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products using advanced instrumentation such as HPLC, GC, UV-Vis spectroscopy, and dissolution apparatus.
* Execute method validation and verification protocols to ensure analytical processes are robust and reliable.
* Maintain and calibrate laboratory equipment, ensuring all instruments are in good working condition and documentation is up to date.
* Handle stability testing programs and monitor samples throughout their shelf-life according to established protocols.
* Document all laboratory findings, results, and observations accurately in line with data integrity standards.
* Investigate Out of Specification (OOS) and Out of Trend (OOT) results, ensuring timely documentation and corrective actions.
Required Qualifications and Skills
* Educational Background: A Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm), Chemistry (B.Sc/M.Sc), or a related Life Sciences field.
* Experience: Relevant experience in a pharmaceutical manufacturing environment (QA/QC) is preferred, though we welcome motivated individuals who demonstrate strong technical knowledge and a fast learning curve.
* Regulatory Knowledge: Solid understanding of cGMP guidelines, FDA, WHO, or other international regulatory standards.
* Technical Proficiency: Hands-on experience with analytical software and laboratory information management systems (LIMS) is highly advantageous.
* Analytical Mindset: Strong problem-solving skills with a keen eye for detail and a proactive approach to identifying quality risks.
* Communication Skills: Excellent written and verbal communication skills are necessary for effective documentation and reporting.
* Team Collaboration: Ability to work efficiently within a multi-functional team environment, coordinating with production, regulatory affairs, and supply chain departments.
Why Join Zenotech Laboratories
At Zenotech, we believe that our employees are our greatest asset. We provide a professional, collaborative, and innovation-driven environment where every employee is encouraged to grow and contribute to our overarching goal of delivering high-quality healthcare solutions.
When you join our team, you gain access to:
* A challenging career path with opportunities for professional development and training in advanced pharmaceutical quality processes.
* A supportive work environment that values integrity, accountability, and excellence in every task.
* Exposure to modern pharmaceutical practices and technology, allowing you to stay at the forefront of the industry.
* A culture that prioritizes safety, compliance, and ethical behavior above all else.
How to Apply
If you are passionate about quality and committed to upholding the highest standards of pharmaceutical manufacturing, we would love to hear from you. Interested candidates should prepare an updated curriculum vitae that highlights their educational qualifications, relevant technical experience, and core competencies.
Please ensure your application clearly states the position you are applying for. Our hiring team will review all submissions, and candidates who meet our requirements will be contacted for an initial screening interview. We value diversity and encourage all qualified professionals to apply for these open positions.
Join us as we continue to push the boundaries of quality and innovation in the pharmaceutical industry. We look forward to receiving your application and exploring how your skills and dedication can contribute to the success of Zenotech Laboratories.