Sterile Operations Supervisor – 1st Shift Lead

Mannkind Corporation

Danbury (CT)

On-site

USD 84,000 - 126,000

Full time

14 days+
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Job summary

MannKind Corporation in Danbury, CT is seeking a Sterile Operations Supervisor to lead daily sterile drug product manufacturing on the 1st shift (M-F, 7am–3:30pm). You will supervise an operator team, coordinate shift activities, ensure safe, compliant execution, and support quality systems on the manufacturing floor.

This role requires 5–7+ years in pharma/biotech manufacturing, preferably with sterile/aseptic operations, and proven supervisory experience.

Qualifications

  • Bachelor's degree in engineering, microbiology, biochemistry, pharma sciences, biotechnology or related field preferred.
  • 5–7+ years of pharmaceutical/biotech manufacturing experience with sterile or aseptic operations.
  • 2+ years of demonstrated lead or supervisory experience.

Responsibilities

  • Supervise daily sterile manufacturing execution across formulation, component prep, isolator filling, inspection, and device assembly.
  • Convert approved production schedule into daily work assignments and coordinate coverage, equipment readiness, materials, and training for a four-operator team.
  • Provide direct people supervision, coaching, attendance oversight, and performance feedback.
  • Verify operators are trained and qualified before independent task execution and address gaps.
  • Lead daily tier meetings, shift handoffs, floor communications, and first-line escalation with cross-functional teams.

Skills

Sterile operations
Supervisory experience
Quality systems
Regulatory knowledge
Training & coaching

Education

Bachelor's degree in engineering or related field
Associate degree or technical credential considered

Tools

QMS systems

Job description

MannKind Corporation in Danbury, CT is seeking a Sterile Operations Supervisor to lead daily sterile drug product manufacturing on the 1st shift (M-F, 7am–3:30pm). You will supervise an operator team, coordinate shift activities, ensure safe, compliant execution, and support quality systems on the manufacturing floor.

This role requires 5–7+ years in pharma/biotech manufacturing, preferably with sterile/aseptic operations, and proven supervisory experience.

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