Quality Manager
Quality Manager
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Job Description
JLL empowers you to shape a brighter way.
Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services advisory and technology for our clients. We are committed to hiring the best most talented people and empowering them to thrive grow meaningful careers and to find a place where they belong. Whether youve got deep experience in commercial real estate skilled trades or technology or youre looking to apply your relevant experience to a new industry join our team as we help shape a brighter way forward.
Job ResponsibilitiesOperationsBuild successful relationships with Life Sciences (LS) client stakeholders to promote confidence in quality and compliance as well as forward management and leadership direction for the development and implementation of quality and compliance with other Life Sciences accounts to proactively accumulate share and reapply all learnings successes as well as best with Global Life Sciences Quality Vertical for development revision and implementation of QMS and quality for ensuring Lide Sciences facilities teams adhere to the required training and ensuring in compliance to clients QMS and quality training for ensuring that the work conducted by the Facilities team and its subcontractors is in full compliance with contractual requirements clients SOPs GxP FDA and other to perform/support internal JLL compliance audits and prepare SOPs and training materials for use by the Life Sciences facilities team in the performance of their Life Sciences facilities team in closing recommendations from clients audit. Expected to interface with the clients quality personnel to ensure that all of the clients SOPs are followed work performed by the LS facilities team is properly documented for traceability in the framework of quality assurance support and develop a Quality Engineering Maintenance program for a controlled-environment manufacturing and laboratory facility as it relates to the facilities maintenance of this plant. Conduct investigations and drive accountability for all quality programs to create value for client to ensure program deliveries meet or exceed quality-relevance investigation via structured Root Cause part of career development lead Life Sciences accounts as an IFM and report on critical & key performance measurements. Develop and submit periodic site status reports related to the Quality ManagementEffectively lead and guide a Life Sciences Quality team by clearly communicating expectations accountabilities and providing performance feedback for continuous Life Sciences Operations team members complete relevant quality and compliance new Life Sciences team members on quality and compliance for their adaptation into specific Life Sciences develop and train peer and direct report team direction/information to vendors facilities staff and service providers as required to ensure that quality assurance expectations are communicated and other quality-relevant duties and tasks assigned. Knowledge Skills & AbilitiesMINIMUM REQUIREDPREFERREDEducation/trainingBachelor degree preferredDegree in science technical or relevant disciplineSound fundamental knowledge in process utilities.6 Years of relevant experience preferred with minimum 4 years in Quality and Compliance discipline in GxP manufacturing or laboratory -Sigma and Root Cause Analysis training is and knowledgeBackground in technical documentationWork independently and within a mindset of compliance and effectively with technical quality assurance and other in Word Excel and other Microsoft Office Suite programsAbility to investigate recognize and diagnose trends and understanding of cGMPs as they relate to the performance of maintenance and repairs to facilities utilities and equipment utilized for the manufacturing plants and laboratories for drug working at an FDA regulated manufacturing facility in a quality assurance or quality control investigations and corrective action plans for appropriate of compliance issues as required collaborating with relevant Compliance Partner(s)Understanding of FDA regulations including 210 CFR part 210 and commitment to quality assurance and a willingness to help develop a quality first culture on the of Quality Engineering techniques CMMS systems and Quality Management SystemsEnglish communication is essentialOther abilitiesGood oral and written communication skills including the ability to communicate to all levels of management and willing to interface with a diverse customer base including technical and non-technical work requirements and work conditionsFamiliar with process utilities and GxP environment.Location:
On-site Mumbai MHScheduled Weekly Hours:
38Job Tags:
Transition ManagementIf this job description resonates with you we encourage you to apply even if you dont meet all the requirements. Were interested in getting to know you and what you bring to the table!
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Required Experience:
Manager
Employment Type
Full-Time
