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Job #03214

About our client Our client is an established CRO that is a leading resource for contract semi-solid and liquid development, manufacturing and packaging services. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. Position Location Quality Assurance Manager – Sterile Operations Lakewood, New Jersey Salary Highly competitive package, commensurate with experience Responsibilities 1) Develop and implement aseptic processing of pharmaceutical products through the management of supervisory and hourly personnel 2) Interface effectively with a variety of support operations like validation, quality, etc. 3) Manage the day-to-day operations of the Supervisor and hourly unionized workforce in producing sterile products via aseptic processes 4) Manage facility at standards required to maintain sterile operations as per cGMPs and FDA guidelines 5) Encourage employee participation and teambuilding 6) Provide leadership for employee development activities 7) Function as a member of a team focused on attaining goals and objectives 8) Understand and comply with company safety, environmental as well as quality practices and procedures outlined in departmental guidelines and SOPs Requirements 1) BA from a four-year college or university 2) 5 – 8 years of experience in production management in an aseptic environment within the pharmaceutical industry 3) 2 years of management/supervisory experience 4) Strong GMP experience 5) Experience in a sterile manufacturing facility 6) Knowledge of sterilization theory and equipment 7) Must be able to organize and prioritize work in order to accomplish tasks assigned 8) Superb problem solving, organizational and communication skills 9) Result-oriented individual