Company Description:
We provide premier business and technology solutions and services for:
IT Service & Support
Web Development & Design
Network & IT Infrastructure Solutions
Hosted & Managed Solutions
Staffing Solutions
Approximately 90% of our business is referral based. Our clients range from end-users, to small business, to large corporation, to national companies. Whatever the size or market of our client, we provide the best-fit solution for their needs
Job Description:
Manufacturing Supervisor- Kansas City, KS
Candidates Must Have:
B.S. and 6+ years, or M.S. and 0 - 4 years
Expertise in pharmaceutical development, specifically formulation and process development experience required.
Must possess technical knowledge in all phases of sterile processing, cleanroom work, and applicable FDA Regulations and Guidelines, requires ability to supervise and motivate technicians and production personnel as needed and have the ability to coordinate the effective utilization of material and personnel.
Background in production, Quality Control, or Research and Development is desired, as is education in Chemistry, Physics and Mathematics.
Responsibilities:
Schedule, plan and direct activities, assign personnel, assure material availability and coordinates with other areas to assure that production requirements are met with the high levels of quality, safety, and cost efficient productivity.
Provides technical knowledge related to sterile processing for use in Production, Research projects, Engineering, Maintenance, Regulatory Affairs, Quality Assurance, Validation, Quality Control, etc. and works with technical staff in those areas to make improvements and solve problems.
Writes standard operating procedures and batch production records, provides input for documents created for Engineering, Validation, QA, Research, etc. Trains and motivates personnel in highly specialized disciplines, including aseptic processing, GMP’s and safety.
Reviews completed production records for accuracy and helps process them and reviews environmental monitoring trends.
Writes job descriptions and conducts annual evaluations of personnel, counseling, hiring interviews, and disciplinary actions if needed.
Qualifications:
Bachelor of Science Degree and 6+ years in a similar role
Expertise in pharmaceutical development, specifically formulation and process development experience required.
Must possess technical knowledge in all phases of sterile processing, cleanroom work, and applicable FDA Regulations and Guidelines, requires ability to supervise and motivate technicians and production personnel as needed and have the ability to coordinate the effective utilization of material and personnel.
Background in production, Quality Control, or Research and Development is desired, as is education in Chemistry, Physics and Mathematics.
ZipRecruiter - 13 months ago
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