Quality Ops End To End Supervisor (9:00pm To 7:00am)

Haleon

Base: $110,178 to $160,000; bonus/equity: 12% perf...
Not specified
Quality systems compliance
Cgmp and regulatory guidance
Batch release assurance
Haleon is seeking a Quality Ops End To End Supervisor for the night shift, responsible for ensuring compliance with quality operations and regulatory requirements in a pharmaceutical environment. The ideal candidate should possess substantial experience in operational quality, management, and strong communication skills, along with a relevant scientific degree

Job Summary

  • Plans, organizes, directs and controls for quality operations activities to assure full compliance with corporate policies and governmental regulations.
  • Provides leadership to the Quality Ops End to End department with responsibility for supporting and developing reports.
  • Haleon offers a robust Total Reward package that consists of competitive pay and a comprehensive benefits program.

Matching Summary

Match Score: 85

Haleon is seeking a Quality Ops End To End Supervisor for the night shift, responsible for ensuring compliance with quality operations and regulatory requirements in a pharmaceutical environment. The ideal candidate should possess substantial experience in operational quality, management, and strong communication skills, along with a relevant scientific degree.

Salary

Base: $110,178 to $160,000; Bonus/Equity: 12% Performance Bonus; Benefits: Comprehensive benefits program including 401(k), tuition reimbursement, 6 months paid parental leave, healthcare

Skills & Requirements

Must-have

  • Quality Systems Compliance
  • cGMP and Regulatory Guidance
  • Batch Release Assurance
  • Supplier Quality Practices
  • Change Control Management
  • Customer Complaint Investigation

Nice-to-have

  • Agile, performance-focused culture
  • Human understanding and trusted science
  • Teamwork and Company Values
  • Conflict resolution and interaction management

Key Requirements

  • Bachelor’s degree in pharmacy, chemistry or related scientific discipline
  • 5+ years in pharmaceutical industry
  • 5 years’ management experience
  • Knowledge of cGMP’s/FDA and other Regulatory requirements
  • Project management and leadership skills
  • Fluent English (oral and written)

Work Rights

Not specified

Tailored Resume

Cover Letter