ZIM Laboratories Ltd., a leading player in the pharmaceutical manufacturing industry, is looking for an Executive in the QA/QC Department. This is a fantastic opportunity for experienced professionals with 5-6 years of expertise in Quality Assurance and Quality Control to contribute to a fast-growing company that values innovation, quality, and regulatory compliance.
About ZIM Laboratories Ltd.
ZIM Laboratories Ltd. is known for its cutting-edge pharmaceutical solutions, specializing in developing and manufacturing high-quality, innovative drug delivery systems. With a commitment to regulatory compliance and maintaining global standards, ZIM Laboratories offers professionals the chance to work in a dynamic environment where quality and continuous improvement are paramount.
Key Responsibilities of the Executive – QA/QC
As an Executive in the QA/QC department, you will be responsible for ensuring that all quality assurance and control processes meet the highest standards of pharmaceutical manufacturing. Your role will involve initiating and performing process validation and equipment and instrument qualification to ensure regulatory compliance. You will also lead Product Quality Reviews (PQR) to maintain product consistency. Handling Out of Specification (OOS) and Out of Trend (OOT) investigations, managing deviations, conducting root cause analyses, and implementing Corrective and Preventive Actions (CAPA) are critical parts of this role, especially in managing market complaints.
In this role, you will ensure balance calibrations comply with Good Laboratory Practices (GLP) and that Finished Goods (FG) meet specification standards. Reviewing logbooks for QMS, manufacturing, packing, QC, and other departments will be part of your daily tasks. You will also prepare and update Standard Operating Procedures (SOPs) and manage incident investigations, deviations, and OOS cases. You will oversee cleaning validation protocols to meet regulatory standards and handle change control processes to ensure audit compliance.
Providing training based on the Training Need Identification (TNI) schedule will be required to maintain team competency. You will implement Total Quality Management (TQM) systems and ensure compliance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). Additional responsibilities include conducting decontamination processes, performing hold-time studies, and analyzing data trends for quarterly and yearly QMS reporting.
Qualifications & Experience
Candidates should have a Bachelor’s or Master’s degree in Pharmacy or a related field and 5-6 years of relevant experience in pharmaceutical quality assurance and control.
Skills Required
In-depth knowledge of QA/QC processes in pharmaceutical manufacturing, expertise in process validation, SOP preparation, and CAPA management are essential. Familiarity with GLP, GMP, and GDP regulations is necessary. Strong analytical skills, experience in managing OOS, OOT, and deviations, and proficiency in change control processes and audit compliance are required.
How to Apply
If you are interested in joining ZIM Laboratories Ltd. and contributing your expertise to a company that values quality and compliance, prepare your updated resume highlighting relevant qualifications and experience. Send your resume to careers@zimlab.in with the subject line: Application for Executive – QA/QC.
