Manufacturing Supervisor I

Manufacturing Supervisor I, II, III

Cheney, Washington

Are you ready to take your manufacturing leadership skills to the next level? We are seeking experienced Manufacturing Supervisors to oversee key aspects of aseptic manufacturing operations, including compounding, preparation, filtration, filling, and lyophilization.

Key Responsibilities

• Supervise assigned manufacturing operations which might include compounding the various antigens manufactured in the ABU portfolio and reporting operational status to the next level of management and with all affected peers on a daily basis.
• Review and update manufacturing documentation associated with the manufacturing areas.
• Provide cGMP, job task, and safety training for personnel in the manufacturing areas.
• Generation, update and maintain area Standard Operating Procedures and BPR’s. Compliance with cGMP through observation, training and auditing.
• Supervise hourly employee performance, including compliance with SOP’s, cGMP’s, and safety regulations.
• Perform deviation investigations related to assigned area of responsibility along with implementing corrective actions to prevent recurrence of such deviations.
• Order production supplies and equipment required to manufacture product.
• Prepare production-monitoring reports and participate in analysis of product cost and budgeting process.
• Interview new employees. Provide coaching and counseling to area personnel. Conduct performance evaluations and set objectives and performance standards for area personnel. Assist next level of management in the implementation of disciplinary action.
• Analyze and make recommendations regarding capital expenditure and efficiency improvements in the manufacturing areas.
• Interact with all supporting departments (ex: Quality Assurance, Maintenance, PIC, etc) to ensure production line problems are dealt with promptly and with appropriate quality considerations.
• Schedule the validation of processes and equipment.
• Ensure that all environmental monitoring limits are maintained in all areas.
  
  

Qualifications for All levels: (Level III SME)

• Microsoft Word, Excel, and PowerPoint
• Managing conflict and influencing outcomes
• Interpretation of cGMP regulations
• Subject to practices/well defined policy, management reviews results after the fact
• Provides analysis, diagnosis or production tasks which noticeably impact end result
• 20 / 30 Corrected Near-Point Vision required.
• Experience working in clean room environments
  
  

Supervisor I

• Bachelor of Science and 6 months related experience OR Bachelors of Arts and 2 years of related experience, OR No degree and 4 years of pharma or supervisory experience.
  
  

Supervisor II

• Bachelor of Science or Arts and 2 years related experience OR No degree and 4 years of pharma or supervisory experience
• Prior supervisory and pharmaceutical experience required
  
  

Supervisor III

• Bachelor’s degree (Science or Arts) with 4 years of relevant experience, OR 5 years of supervisory and pharmaceutical experience without a degree.
• Proven experience managing conflict, influencing outcomes, and interpreting cGMP regulations.
• Cleanroom experience preferred.
  
  

Compensation:

• Salary range: $75,500–$160,100 (based on experience). Opportunities for growth, promotion, and annual raises are available.
  
  

Please reach out to Kiera Kelleher at Kiera@Scientificsearch.com

Please reference job# 19077 when you reach out!