SUPERVISOR, QUALITY CONTROL LAB

ADP; Irvine (CA); On-site; USD 96,000 - 110,000; Full time

Job summary

LGM Pharma in Irvine, CA is seeking a Supervisor of Quality Control Lab to oversee daily QC activities, set priorities, and guide staff in a GMP environment. You will ensure accurate review of results and maintain calibration schedules across instruments like HPLC, GC, CE, ICP, FTIR, TOC, and dissolution.

The role requires a bachelor’s degree in chemistry, 8+ years in a GMP analytical laboratory, and proven leadership to drive performance and compliant operations within the laboratory team.

Qualifications

• Bachelor’s or higher degree in Chemistry or related discipline, or equivalent combination of education and experience.
• 8+ years’ experience in a GMP analytical chemistry laboratory, including analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus.

Responsibilities

• Supervises the daily activities of the QC laboratory chemist by establishing testing priorities and schedules and assignments of staff.
• Provides daily direction, guidance and feedback to employees based on work priorities and schedules.
• Assures appropriate review of analytical results commensurate within the company review policy.
• Conducts employee performance review, compensation reviews and new employee recruitment.
• Supervises and performs laboratory investigations.
• Maintains equipment calibration schedule and ensures that all required calibrations and maintenance are completed in a timely fashion.
• Authors standard operating procedures and assist with revision process of current procedures.
• Ensures laboratory compliance with applicable regulations.
• Performs and/or assists with procedural, cGMP, and safety training of laboratory staff.
• Acts as communication liaison for laboratory with other facility departments.
• Serve as backup for laboratory Management.
• May performs analytical testing of raw materials, in-process samples, and finished products using analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus as necessary.
• Assists with preparations for internal and external laboratory audits and inspections.
• Other related duties as required.

Skills

Lead capacity

GMP analytical chemistry

Communication skills

Organization & prioritization

Detail orientation

Education

Bachelor’s degree in Chemistry or related discipline

Tools

Analytical instrumentation: HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

SUPERVISOR, QUALITY CONTROL LAB

Full Time Exempt Irvine, CA, US

2 days ago Requisition ID: 1129

Salary Range: $96,000.00 To $110,000.00 Annually

RESPONSIBILITIES:

• Supervises the daily activities of the QC laboratory chemist by establishing testing priorities and schedules and assignments of staff.
• Provides daily direction, guidance and feedback to employees based on work priorities and schedules.
• Assures appropriate review of analytical results commensurate within the company review policy.
• Conducts employee performance review, compensation reviews and new employee recruitment.
• Supervises and performs laboratory investigations.
• Maintains equipment calibration schedule and ensures that all required calibrations and maintenance are completed in a timely fashion.
• Authors standard operating procedures and assist with revision process of current procedures.
• Ensures laboratory compliance with applicable regulations.
• Performs and/or assists with procedural, cGMP, and safety training of laboratory staff.
• Acts as communication liaison for laboratory with other facility departments.
• Serve as backup for laboratory Management.
• May performs analytical testing of raw materials, in-process samples, and finished products using analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus as necessary.
• Assists with preparations for internal and external laboratory audits and inspections.
• Other related duties as required.

REQUIRED QUALIFICATIONS:

• Bachelor’s or higher degree in Chemistry or related discipline, or equivalent combination of education and experience.
• 8 + years’ experience in a GMP analytical chemistry laboratory, including analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus.
• Demonstrated ability to act in a Lead capacity and provide direction to others.
• Ability to build relationships at all levels of the organization.
• Strong communication and demonstrated listening skills.
• Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision.
• Strong attention to detail.

At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.