[BioTechies] Process Chemist
Responsibilities: • To monitor QMS & GMP • To ensure all activities are carried out according to the quality plan and all raw materials are adequate and correct as per…
Responsibilities: • To monitor QMS & GMP • To ensure all activities are carried out according to the quality plan and all raw materials are adequate and correct as per…
Position Summary: The CRO/CRA Executive will play a critical role in the execution of clinical trials within a cGMP-compliant cell therapy and advanced biologics pipeline. This position is responsible for…
Job Description We are looking for a highly driven individual to join as a Production Executive in the field of cancer immunotherapy and human stem cells. Candidate will work closely…
Job Scope: Operate and maintain equipment and the facility to ensure that our products are manufactured and delivered to the customer on time, made at the best cost, safely and…
Join Us as a Clinical Research Associate At Klinsel, we are committed to delivering excellent services to our clients and are passionate about quality. In this fast paced and ever-growing…
Job Description: We are looking for highly driven individual to be part of our team as Quality Control Associate. Candidate is expected to have laboratory and human cell culture skills and…
Role Purpose: To support Drug Substance (DS) and/or Drug Product (DP) operations by assisting in day-to-day execution, documentation, sampling, basic data analysis, and adherence to GMP and EHS requirements, ensuring…
Join our growing team dedicated to producing high-quality food products with excellence, safety, and integrity. We are looking for a hands-on and motivated Production Supervisor to oversee daily production operations…
We are looking for a Quality Assurance (QA) Executive to support and maintain GMP and quality systems in our manufacturing facility. This role is ideal for candidates who are detail-oriented,…
Role summary: Provide operational, regulatory, and documentation support for interventional and procedural clinical trials in human therapeutics and medical-device-associated procedures. Key responsibilities: maintain Trial Master File and regulatory/consent documentation; support…