As a CQV Engineer, you will be responsible for ensuring the successful commissioning, qualification, and validation of equipment, systems, and processes within client’s pharmaceutical plant.
You will play a crucial role in maintaining compliance with industry regulations, optimizing operational efficiency, and ensuring the quality and safety of the products.
Bachelor’s degree in Engineering, Life Sciences, or a related field. Certification in CQV or related areas, will be added advantage. Strong knowledge of GMP, FDA, and EMA regulations, and experience in regulatory inspections and audits. Proficiency in using validation software and tools. Minimum 5 years of experience in commissioning, qualification, and validation within the pharmaceutical industry. Experience with risk assessments, validation protocols (IQ, OQ, PQ), and technical writing. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Ability to work independently and as part of a team. Attention to detail and commitment to quality. undefined