Packaging Supervisor

Nova Biomedical One Global Brand One Vision Together under one name Advanced Instruments and Nova Biomedical are now united under one brand Nova Biomedical marking a major milestone in our journey to deliver greater value to our customers By combining our strengths were accelerating innovation supporting critical workflows and delivering world class service across the biopharmaceutical and clinical markets

This individual has shift responsibility for day to day activities of Packaging within Reagent Manufacturing This includes overseeing scheduling of all packaging activities such as calibrator packs external standards and miscellaneous reagents Controls as well as Auto QC products for Nova core and OEM products Short term goals are to deliver products to customers on time with high quality and minimal scrap Long term goals include continuous improvement of packaging operation personnel and processes utilizing resources such as R&D Planning Purchasing QAQC and Consumable Manufacturing Engineering

• Manage the daily packaging schedules on assigned shift to deliver product on a timely basis so that demand for Finished Goods is met
• This may include pilot requests from R&D and Consumable Manufacturing Engineering Coordinate with other shift supervisors to ensure delivery of products and smooth and effective transition between shifts
• Work closely with Master Scheduling R&D Manufacturing Engineering and Purchasing to meet demand of customers by ensuring quality and on time delivery of raw materialsupplies
  
  Ensure adequate training of Packaging personnel overtime control reducing scraps labor utilization improving workflow efficiency and cost reduction
• Oversee all safety aspects of Packaging on shift
  
  Participates in Reagent waste management
  
  Interviews hires trains develops coaches motivates and evaluates staff
  
  Conduct performance appraisals for employees reporting to this position address resolution of employee issues and enforce Nova policies
  
  Ensure all Packaging equipment is adequately maintained and qualified for daily usage
  
  Monitor and control product scrap and create defect awareness
  
  Review as needed of Device History Records DHRs prior to submitting to QCPerform other duties as assigned

• Minimum 3 years experience in an Assembly Packaging or comparable environment is required
• Minimum 3 years experience in a supervisory role in manufacturing or comparable environment is required
• Minimum 3 years experience in a GMP environment
• Minimum 3 years experience in a regulated safety environment OSHA safety standards
• Minimum 3 years experience in a Quality System Regulations QSR
• Working knowledge of SAP or similar MRP system is desired
• Working knowledge of Master Control or similar system is desired
• FDA TUV and customer audit experience is a plus
• Basic Knowledge of Non Conforming Material Report NCMR and Material Review Board MRB process
• Lean Manufacturing knowledge is a plus

Must be able to perform tasks that may involve extended periods of standing sitting pushing pulling lifting bending kneeling reaching twisting turning climbing steps and carrying up to 25 pounds numerous times hours a day Require repetitive use of armswristhands while setting upworking with equipmentraw material throughout the dayWill require use of Personal Protective Equipment PPE and may include but not limited to safety glasses safety shoes lab coat bouffantbeard guard gloves hearing protection face shield nuisance mask bump capMust have good handeye coordination and visual acuity

Must be able to distinguish colors

• Flexible Medical Dental & Vision Coverage
• Competitive 401k company match
• Bonus Program
• Generous PTO and paid…