knowledge of quality assurance, familiarity with manufacturing environments, knowledge of equipment and processes, ability to read and understand product specifications. Must be able to measure and interpret measurements up to a 1/16th of an inch using rulers, and have good basic math skills with ability to add, subtract, multiply and divide with ease.
Must be able to occasionally lift and/or move up to 40 pounds w/out help Must be able to bend, crouch, walk, stand, push, and sit throughout entire shift. Must be able to fluently speak and understand verbal insurance in English Must be able to sufficiently read and write in English to follow work order instructions and prepare simple production
reports. Activities required: Near vision, mid-range vision Data entry, keyboarding, talking, hearing, detailed work with hand motions The Quality Inspector at Technipaq is a key player in performing routine checks, tests, gauging, and instrument inspections of materials, goods in-process, and finished goods to keep productivity at peak levels 24-hours a day.
The Quality Inspector report to our Quality Manager and interact with all levels of the company in order to make sure customer specifications and quality guidelines are met. Technipaq is family owned and operated serving the medical device and medical packaging industry since 1984. We started as a small one machine company and now
operate over 100,000 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. NO PHONE CALLS PLEASE! We will contact applicants for an interview if interested. Thank you.
in a production environment, preferably in flexible packaging Good knowledge and minimum of 3 years working as Q. E. in an ISO 13485 environment is required Previous experience doing customer complaint investigation process, including root cause analysis on the production floor and customer contact and interaction is required since this will be their primary focus for first 6 months to a year.
Previous ERP/MRP experience required Proficient in MS Office (Excel, Word and Power Point and Outlook) required 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 Engineer's overall purpose is to work within the Quality team to ensure the quality of the company's products are in line with ISO 13485 compliance.
They are responsible for understanding the underlying quality issues, developing successful fixes, and changing practices where necessary to ensure that standards are maintained. The Quality Engineer works with the Engineering, Production, and Management teams, Technipaq suppliers and customers and plays a key role in fixing issues when they arise. The Quality Engineer works under minimal supervision of the Quality Manager. Technipaq is family owned and operated serving the medical device
and medical 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.
employee contributions and 75% of the next 2% of employee contributions; no vesting period - 100% vested from day 1 Health Savings Account (HSA): the company will contribute $1,000 for employee only coverage and $2,000 for family coverage, annually Free Short Term and Long-Term Disability Insurance Free Basic Life and Accidental Death & Dismemberment (AD&D) insurance at an amount that is 2x Annual Salary Wellness Program Competitive Vacation Accrual schedule and 10 paid Holliday's SUMMARY OF POSITION: Responsible for ensuring that the products produced meet quality standards required to minimize quality costs and maximize customer satisfaction while ensuring that procedures and processes are
adhered to.
Ensure incoming materials meet required quality standards. Responsible for identifying and raising quality issues and for efficiently resolving them to ensure zero impact to the customer.
Support new product introductions to ensure the robustness of product builds. Work in a team environment to develop and implement best practices that emphasize defect prevention, reduction in variation and waste and provide for continuous improvements in meeting all customer requirements. ESSENTIAL RESPONSIBILITIES: Manage all quality-related issues for internal, customer, and supplier. Interface contact to customers and suppliers as assigned. Interface internally with all functions
as necessary to resolve quality issues and/or drive improvement events.
Travel as needed to customer and/or supplier as assigned. Work with internal and external interested parties to resolve quality issues that arise as quickly and efficiently as possible to prevent compromising quality and safety standards. Problem Solving Understanding of problem-solving tool methods such as: brainstorming, 8D methodology, CAPA, 5 Why, Fishbone Diagram, Pareto Charts Baseline understanding of quality statistics. Identify, investigate, and analyze root cause(s) for product/process quality issues and/or improvement events. Identify, evaluate, and verify corrective/preventive action(s) for product/process quality issues, and/or improvement events.
Ensure compliance and assist with adherence to the Quality Management System. Create, implement, and document quality acceptance requirements according to site procedures. Ensure Control Plans, FMEAs and associated documentation are implemented effectively and maintained. Evaluates non-conforming product and disposition. Participate in multi-functional teams in the development of new products or changes related to current products in meeting customer requirements. If this sounds like you, we should talk. We help forward-thinking companies the world over create more innovative, higher performing products.
Of course, we can only do this because we combine pioneering technology with the best people on the planet. People dedicated to getting the job done, no matter what. Build your future with Dynacast - let's get to work. QUALIFICATIONS and COMPETENCIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or competencies required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Knowledge and understanding of Core Tools: MSA, SPC, Control Plans, FMEA, APQA, and PPAP. Understanding of a quality related software system. Must be well-organized and proficient in Microsoft Word, Excel and Power Point. EDUCATION and/or EXPERIENCE Bachelor's degree from four-year college or university; or two to three years related experience and/or training; or equivalent combination of education and experience. Bi-lingual (English / Spanish) a plus.
