Chemical Manufacturing Manager

Cytosorbents Medical Inc
Full time Full day
White Horse, NJ

CytoSorbents Inc, a critical care immunotherapy leader, is seeking to fill a Chemical Manufacturing Manager role at its Monmouth Junction, NJ location - soon to be moving to a fantastic new facility in Princeton! This role is responsible for managing cGMP compliant activities associated with mixing chemicals to produce porous polymer beads used in our lifesaving, blood purification medical device products.


  • Accomplishes objectives by managing the cGMP compliant chemical manufacturing of porous polymer beads

  • Evaluates, plans and organizes daily activities and production schedules and ensures all staff are performing their assigned tasks properly

  • Ensures operations are conducted in a safe, high-quality, compliant, and efficient manner

  • Responsible for achieving planned shift outputs while ensuring quality standards are met

  • Facilitates communication between shifts

  • Liaises with managers in QC, Engineering, and R&D to coordinate overlapping workflows

  • Coordinates with QC regarding delivery and receipt of samples, WIP, and RM’s

  • Receives notifications from Engineering and/or Quality to make specified operating adjustments

  • Conducts investigations as related to Deviations, NCMRs, and CAPAs and provides necessary documentation to support proper close out

  • Takes part in production leadership meetings and initiatives to support company goals of building a continuous improvement environment

  • Performs minor equipment maintenance and calibrations as needed

  • Responsible for hazardous material and safety management within facilities

  • Manages shift personnel which includes performance evaluations, PTO requests, time clock reconciliation

  • Oversees training of employees on designated process operations

  • Solicits employee suggestions for improvements and implements as appropriate

  • Coaches, counsels, and disciplines employees

  • Regular working hours are M-F from 8:30 am – 5:00 pm but must be available at times to meet with other manufacturing personnel on other shifts

  • Other duties as assigned

. Requirements:
  • Bachelor’s degree in Chemical Engineering, Chemistry or related discipline and 8+ years of experience including 3+ years as a supervisor or manager in a cGMP manufacturing facility

  • Understanding of quality standards and health & safety regulations

  • Knowledge/implementation of Continuous Improvement, Six Sigma and Lean Manufacturing/5S

  • Outstanding communication, organizational and leaderships skills

  • Strong decision-making skills, attention to detail and a results-driven approach

We offer a friendly, team-oriented environment with competitive benefits plus stock options.

Candidates must be legally authorized to work in the US and will not require sponsorship now or in the future.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, disability status, or any other characteristic protected under applicable law.

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