Quality Supervisor

Technipaq, Inc.; Crystal Lake (IL); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

401(k) with match

Paid holidays

Job summary

Technipaq, Inc. is seeking a Quality Supervisor to oversee production quality personnel and processes in our facilities. The role ensures proper procedures, staffing, and training, while coordinating quality inspections and enforcing ISO 13485 standards.

The position operates with minimal supervision and provides backup support to the QA Manager. Ideal candidates have 2+ years of QA Lab Supervisor experience in ISO 13485, plus strong MS Office and regulatory knowledge.

Qualifications

• Requires 2+ years of QA Lab Supervisor experience in an ISO 13485 environment.
• Experience in flexible packaging industry is preferred.
• Proficient in MS Office (Excel, Word, PowerPoint, Outlook).
• ERP experience is a plus and SPC software experience is required.
• Strong knowledge of regulatory requirements in ISO 13485.
• Good organizational skills and ability to communicate with others.

Responsibilities

• Oversight of production quality personnel and processes, ensuring procedures are followed.
• Manage shift staffing, training, and on-time completion of tasks.
• Coordinate supervision of quality inspection personnel.
• Act as primary driver for ISO 13485/ISO 13845 standards enforcement.
• Operate under minimal supervision and back up QA Manager functions as needed.

Skills

QA Lab Supervisor experience

ISO 13485 knowledge

MS Office

ERP experience

SPC software experience

Regulatory compliance

Communication skills

Cross-functional collaboration

Packaging industry experience

Education

HS Diploma or equivalent

Associate or Bachelor degree preferred

Job description

Shift Available

• 8:00 am to 4:30 pm M-F, with additional hours of 2:00 pm to 10:30 pm or extended hours, once per week, to help 2nd and 3rd shift direct reports.

Required Skills

• Must be at least 18 years or older and pass our pre-employment Reading and Ruler tests.
• Associate or Bachelor degree preferred, HS Diploma or equivalent required.
• Must have 2+ years of QA Lab Supervisor experience in an ISO 13485 environment required.
• Flexible packaging industry experience is preferred.
• Proficient in MS Office (Excel, Word and PowerPoint and Outlook) required.
• Previous ERP experience is a plus.
• SPC software experience is required.
• Strong knowledge of all regulatory requirements in an ISO 13485 environment.
• Strong organizational skills and ability to effectively communicate and share knowledge with others required.
• Works well with other departments in communication of timelines, priorities and resolving ambiguous tasks/situations.

The Quality Supervisor is responsible for the oversight of production Quality personnel and processes, including: ensuring the proper procedures are in place, managing shift staffing, ensuring adequate training with on time completion, and coordinating the direct supervision of quality inspection personnel. They will act as primary driver for the enforcement of ISO 13845 standards within the production and quality lab environment. This position works under minimal supervision and serves as a backup to some of the Quality Assurance Manager functions.

Technipaq is family owned and operated serving the medical device and pharmaceutical packaging industry since 1984. We started as a small one machine company and now operate over 160,000 square feet of manufacturing space with 3 manufacturing and warehouse facilities and 180+ employees. Our manufacturing facilities perform the laminating, slitting, sheeting, die cutting, fabricating, and flexographic printing of pouches, lids and roll stock produced in a variety of sizes from foil, film, Tyvek and paper laminates.

We offer employees a full benefits package including medical, dental, vision, paid Sick and Vacation time, 401(k) with a company match, and paid holidays.