Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk:Ased compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients. What You Will Achieve You will be a member of Pfizers dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Confidencial provide safe drugs to patients. Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R and D. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ility to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. It is your hard work and commitment that will make Confidencial ready to achieve new milestones and help patients across the globe. How You Will Achieve It Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team. Lead efforts to improve process performance, procedures and reporting to meet changing quality and regulatory compliance. Confidencialto create, review, and approve compliant test method transfer and validation protocols and reports and equipment qualification/computer validation records. Perform tasks associated with maintaining Current Good Manufacturing Practices part of GxP compliant Quality Control and Stability laboratories. Support preparation of media, receipt, storage and handling of Bio ball cultures, and investigations related to microbiology. Perform testing including, but not limited to clinical and/or commercial product, raw materials, validation, stability, and Environment Monitoring samples. Support detailing requirements for Laboratory Information Management System builds, building, testing and managing its Master Data changes. Review and authorize all laboratory data and have an extensive Confidencial knowledge of all laboratory operations. Serve on functional teams to represent Quality Control and facilitate communications and activities/projects Perform safety inspection of laboratories and surrounding office area as assigned and prepare a report. Participate in out:Of:Ecification and failure investigations and recommend corrective actions and demonstrate problem solving ilities. Train junior colleagues and may develop training plans and/or oversee training activities for groups. Qualifications Must:Have Bachelors Degree 3+ years experience Technical Skills Experience in handling of Microbiology calibration failures and trouble shooting Experience in microbiological equipments calibration Understanding of pharmaceutical manufacturing, packaging, and quality assurance operations Detail oriented with Quality systems knowledge Excellent effective written and verbal communication and interpersonal skills ility to work in a team environment Nice:To:Have Masters degree Relevant pharmaceutical experience 3 to 5 years Knowledge of computer system hardware, infrastructure and networks Calibration of Microbiology equipments like auto clave, Bio incubators, microplate spectrophotometer, Micro pippetes, Refrigerators and freezers etc. Experience on change control initiation and implementation. Handling of microbiology cal
