Assistant Quality Manager-Medical Device
Schaumburg, IL, US
Scientific
Bachelors Degree
Full Time, Temporary
$45 per hour
Manager (Manager/Supervisor)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Schaumburg, IL, US
$45 per hour
Manager (Manager/Supervisor)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Assistant Quality Manager
- Industry: Medical Device / Personal Care / Food
- Work Schedule: Monday – Friday, 8:00 AM – 5:00 PM
- Job Status: Contract
- Location: Schaumburg, IL area
Position Summary
We are seeking an experienced Assistant Quality Manager to monitor quality levels across all operational areas to ensure compliance with company goals and objectives. In this role, you will support quality assurance and production personnel to achieve cost-effective manufacturing of consumer health and oral care products that consistently meet industry standards and customer requirements. You will also provide direct leadership and supervision to our QA Floor Inspectors and QA Receiving Inspectors.
Key Job Functions
- Team Leadership & Supervision: Oversee QA Inspectors on the manufacturing floor (across all three shifts) and QA Receiving Inspectors handling purchased products, components, and raw materials. Manage time, attendance, annual performance reviews, and professional development plans.
- Training & Compliance: Create, maintain, and execute annual training plans. Train direct reports on applicable policies, standard operating procedures, standard test methods (STMs), AQLs, and environmental safety protocols.
- Documentation & Database Management: Create, revise, and maintain quality electronic records, standard operating procedures, work instructions, and databases (including Finished Goods Inspection, Purchased Products Inspection, NCRs, Deviations, and CODs).
- Quality Control & Audits: Monitor the Control of Non-Conforming product process, ensuring internal audit corrective actions are addressed, processed, and verified. Support the Internal Audit program by acting as an Auditor or Lead Auditor when needed.
- Cross-Functional Support: Assist departments in developing required documentation and procedures, and support Wet Manufacturing operations with resources and training as needed.
Education, Knowledge, Skills, and Abilities
- Education:
- Bachelor’s Degree in a Scientific discipline.
- Quality Assurance Certifications are strongly preferred.
- Bachelor’s Degree in a Scientific discipline.
- Knowledge & Experience:
- Minimum of 5 years of experience in Quality Assurance.
- Prior supervisory experience.
- Strong working knowledge of Quality Management Systems (QMS) and proficiency in interpreting product specifications and part drawings.
- Experience with Access databases.
- Minimum of 5 years of experience in Quality Assurance.
- Skills & Abilities:
- Proficient in MS Office applications, Adobe, database management, and enterprise software (e.g., PDXpert, Integrify).
- Excellent written, oral, and interpersonal communication skills, with the ability to interact effectively across diverse backgrounds and all levels of the organization.
- Exceptional organizational skills and attention to detail.
- Proficient in MS Office applications, Adobe, database management, and enterprise software (e.g., PDXpert, Integrify).
For immediate consideration, please forward your updated resume.
10379039
I want more jobs like this in my inbox.
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.