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Sr. Director Quality Affairs

Job in Shirley, Suffolk County, New York, 11967, USA
Listing for: Randstad USA
Full Time position
Listed on 2026-08-20
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Data Analyst
Salary/Wage Range or Industry Benchmark: 275000 USD Yearly USD 275000.00 YEAR
Job Description & How to Apply Below

Job Summary

Step into a high-impact executive leadership role with a premier global pharmaceutical manufacturer in Shirley, NY. We are seeking a Sr. Director Quality Affairs to provide strategic leadership across site-wide compliance, laboratory operations, and quality management systems. Operating on-site in a cGMP environment, this role offers an outstanding platform to direct regulatory agency interactions and champion continuous quality improvement across all phases of production.

location:
Shirley, New York
job type:
Permanent
salary: $275, per year
work hours: 9 to 5
education:
Bachelors

Responsibilities
  • Provide leadership for site Quality Management Systems, including Dev, CAPA, Change Control, Document Control, and batch release oversight.
  • Lead all regulatory authority inspections (e.g., FDA, Health Canada) and manage post-inspection improvement plans.
  • Direct Quality Control laboratories (Stability, Chemistry, Microbiology, EM) and shop-floor manufacturing oversight.
  • Partner cross-functionally with Production, Engineering, and R&D to implement new technologies and process improvements.
  • Drive site-wide metrics, KPIs, and continuous quality culture across commercial and R&D products.
Qualifications Required
  • Bachelor's degree in Life Sciences or a related field.
  • Minimum 15 years of progressive pharmaceutical operations experience with direct regulatory agency interactions.
  • Minimum 10 years leading functional QA, QC, compliance, or manufacturing operations.
  • Proven history of direct FDA inspection interaction and hands-on shop-floor cGMP leadership.
Preferred
  • Master's degree in Life Sciences.
  • Experience in sterile injectables manufacturing and packaging operations.

skills:
Good Manufacturing Practices (GMP), Quality Assurance (QA), Sterile Manufacturing, Regulatory Audit Preparation

Equal Opportunity

Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

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