Why Patients Need YouEverything 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 AchieveYou will help us in investigation of our quality issues in manufacturing and quality laboratories. You will investigate deviations and out:Of:Ecification results and atypical result investigations. Your problem solving skills will help to identify root cause and suggest appropriate corrective action plan. Your attention to detail will help us ensure that the reports are aligned to regulatory requirements and company policies.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 help in making Confidencial ready to achieve new milestones and help patients across the globe.How You Will Achieve ItContribute to the completion of complex projects and manage own time to meet agreed targets.Develop plans for work activities on own projects within a team.Perform, lead and review deviation investigation reports, change control and validation/qualification.Provide direct input or coaching support for other functional groups in investigations.**Qualifications**:Must:HaveBachelor or Master Degree in Pharmaceutical Sciences7+ years experience in Chemical Laboratory or chemical laboratory Quality Assurance, specifically in sterile Injectable manufacturing facilityAt least 3+ years of experience in conducting/reviewing and approving the laboratory investigationsTechnical experience in laboratory testing and validation processes. Must have handled the HPLC, GC and UV spectrophotometer etc.Proven record of problem solving, decision:Strong background and knowledge in manufacturing, compliance and technology investigations, processes and systemsMust be comfortable working both independently and collaborativelyEffective communication skills are required, both written and verbalComputer literate, with superior skills in managing Excel spreadsheetsNice:To:HaveGreen Belt/Black Belt certificationExperience in eQMS/Trackwise, SAP, gLIMS and EAMSWork Location Assignment:On PremiseConfidencial is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Quality Assurance and ControlLI:PFE
