Quality Operations Technician, 1st Shift

Apex Consumer Products; Eden Prairie (MN); On-site; USD 36,000 - 41,000; Full time

Benefits offered by this job

Medical benefits

Dental and vision benefits

401(k) retirement plan with match

Life Insurance

Job summary

Apex International in Eden Prairie, MN is seeking a Quality Operations Technician to audit manufacturing lines, evaluate materials, and support GMP compliance in a fast-paced, on-site role.

You will document deviations, assist with CAPA, maintain records, and help drive continuous improvement while training staff and promoting a culture of quality. This full-time position offers competitive hourly pay with comprehensive benefits.

Qualifications

• Knowledge of cGMP and 21 CFR manufacturing regulations.
• Strong organizational, multitasking, and problem-solving skills.
• Effective interpersonal communication and coaching abilities.
• Proficiency with Microsoft Office applications.
• Ability to read and follow written work instructions and specifications.

Responsibilities

• Audit manufacturing lines and facility operations for GMP compliance.
• Complete packaging batch records and quality documentation.
• Document and escalate deviations and OOS situations.
• Ensure SOPs and test procedures are followed.
• Maintain and improve SOPs, forms, and test methods.
• Record and analyze quality data to identify trends.
• Support root cause investigations and CAPA activities.
• Promote quality awareness and a culture of quality.

Skills

cGMP knowledge

21 CFR knowledge

Organizational skills

Multitasking

Problem solving

Interpersonal skills

Coaching

MS Office

Read work instructions

Fast-paced environment

Education

Bachelor's in Chemistry

Bachelor's in Biology

Equivalent experience

Tools

Microsoft Office

Job description

About The Role

Apex International is seeking a Quality Operations Technician to join our Quality team in Eden Prairie, Minnesota. This is a full-time, on-site position responsible for auditing manufacturing operations, evaluating raw materials, bulk materials, and finished products, supporting quality and compliance activities, and driving continuous improvement efforts within a GMP manufacturing environment. This role works closely with production personnel to ensure products meet customer expectations, regulatory requirements, and internal quality standards. The ideal candidate is detail-oriented, organized, and passionate about building a culture of quality while supporting world-class manufacturing operations.

Key Responsibilities

• Perform audits of manufacturing lines and facility operations to ensure compliance with quality standards, procedures, and GMP requirements


• Complete required packaging batch records and quality documentation


• Document, investigate, and escalate deviations, non-conformances, potential quality issues, and out-of-specification (OOS) situations


• Ensure compliance with SOPs, work instructions, test procedures, and regulatory requirements


• Support the maintenance and improvement of SOPs, work instructions, controlled forms, and test methods


• Maintain accurate documentation and records in accordance with GMP requirements


• Provide technical guidance, process direction, training, and coaching to manufacturing personnel


• Promote quality awareness and help foster a culture of quality throughout the facility


• Verify products meet specifications and customer standards prior to release


• Maintain product specifications, standards, and reference materials


• Accurately record and analyze quality data to identify trends and resolve recurring issues


• Participate in root cause investigations and support corrective actions to prevent recurrence


• Maintain compliance with current regulatory expectations and practices


• Support Lean initiatives, waste reduction efforts, and 5S activities within the department


• Perform additional duties as assigned

QualificationsRequired

• Working knowledge of cGMP and 21 CFR manufacturing regulations


• Strong organizational, multitasking, and problem-solving skills


• Strong interpersonal, communication, and coaching skills


• Proficiency with Microsoft Office


• Ability to read and follow written work instructions and specifications


• Ability to work effectively in a fast-paced manufacturing environment

Preferred

• Minimum of two years of experience in a GMP manufacturing environment such as pharmaceutical, cosmetics, personal care, food processing, or medical device manufacturing


• Bachelor's degree in Chemistry, Biology, or a related science discipline, or equivalent experience

Schedule

Shift: 1st Shift, Monday through Friday from 6:00AM - 2:00PM

This is an on-site position located in Eden Prairie, Minnesota. Additional hours beyond the regular work schedule may be required based on production demands, customer requirements, and business needs. Periodic overtime and weekend work may be necessary.

Benefits

• $26 - $30 per hour base pay depending on experience


• Medical, Rx, Dental and vision benefits


• Company paid Short term & Long-term Disability


• Company paid Life Insurance


• Optional Life Insurance for employee, spouse and children


• Flexible Spending Account options for child and health care


• 401(k) Retirement Plan with company match


• Employee Assistance Program

Salary: $26.00 - $30.00 per hour