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Manufacturing Manager

Job in Tustin, Orange County, California, 92681, USA
Listing for: Kinetic Personnel Group, Inc
Full Time position
Listed on 2026-07-09
Job specializations:
  • Manufacturing / Production
    Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Production Manager
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

The Supervisor, Manufacturing – Downstream is responsible for leading downstream manufacturing operations and supervising production staff while actively participating in hands‑on processing activities. This role ensures all production is carried out in full compliance with current Good Manufacturing Practices (cGMP) through direct floor presence, oversight, and continuous improvement of processes.

Key Responsibilities
  • Supervise and lead downstream manufacturing staff to ensure safe, efficient, and compliant operation
  • Schedule, plan, and coordinate daily production activities to meet operational goals
  • Perform hands‑on purification processes, including column chromatography, tangential flow filtration, nano‑filtration, and aseptic bulk filling, as needed
  • Ensure accurate and compliant cGMP documentation practice
  • Initiate, revise, and review Batch Production Records (BPRs), Batch History Records (BHRs), SOPs, and associated forms
  • Identify, investigate, and document deviations (IRs/DRs/CAPAs), and ensure timely implementation of corrective and preventive action
  • Develop and maintain SOPs to ensure compliance with regulatory requirements and internal standards
  • Coordinate manufacturing, validation, and maintenance activities with cross‑functional team
  • Support the implementation of new manufacturing processes and critical equipment
  • Identify and resolve technical, procedural, and equipment‑related issues impacting production and compliance
  • Assist in technology transfer from Process Development to GMP Manufacturing
  • Support investigations, inspections, and regulatory audit
  • Promote and enforce safety standards; report unsafe conditions to EHS or leadership
  • Manage and develop direct reports, providing guidance and escalating issues as needed
  • Participate in continuous improvement initiatives and other duties as assigned
Qualifications
  • Bachelor’s degree in Biology, Biotechnology, Chemical Engineering, or related field, or equivalent combination of education and experience
  • 3–5 years of cGMP downstream purification experience
  • Minimum of 3 years of supervisory experience in downstream processing
  • Proven ability to lead teams and drive efficient, compliant manufacturing operations
Preferred Qualifications
  • Bachelor’s degree in life sciences or a closely related discipline
  • Demonstrated leadership in building and improving floor operations within a regulated manufacturing environment
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