Quality Control Specialist

Job Description

The role is responsible for coordination and management of analytical equipment related activities as well as to provide scientific analytical Support. This includes the evaluation, development and validation of methods required for raw materials and finished products. -Performs qualitative and quantitative analyses of organic and inorganic compounds to determine the identity, purity and homogeneity of drug substances and products related to each project. -Organizes and interprets all data obtained using a wide variety of instrumental technologies Major accountabilities: Proofread creatively and digitally developed products to verify their authenticity with respect to the guidelines. Identify defects and log them using a defect form. Liaise with different stakeholders in case of defect rejection. Proficient in various tactics such as RTEs, banners, websites, CAT tools, etc. Hands-on experience with quality checks for complex projects or functional testing as per the project requirements/capacity constraints. Responsible for the quality of the multichannel digital content delivered to customers. Partner with all teams to understand and implement systemic controls wherever possible, across the software supply chain, from design till release. Explore and adopt quality improvement tools or methodologies. Write, control, and manage process documentation. Proven ability to work effectively with cross-functional teams in a matrix organization. Excellent communication and documentation skills. Proficient in MS Word and Excel. Work Experience: Minimum 6-10 years of experience in proof reading and functional testing with a graduate / post graduate degree Expert in proof reading and intermediate in testing proficiency Experience in the creative digital field is desired. Experience in data management and metrics reporting will be an added advantage. Knowledge of healthcare, pharma will be an added advantage.