$1000 Sign-On / Retention Bonus: $250 after 2 full weeks of work & $750 after successfully completing of intro Evaluation

The Quality Assurance Lab Technician is responsible for monitoring the quality of manufactured foam products and raw materials by conducting chemical and physical testing of materials in preparation for final release. They also assist with development and implementation of new procedures, standards and specifications as required by ISO Quality Management Systems.

Required Qualifications

• High school diploma or equivalent

Preferred Qualifications

• Minimum 1 year quality related industrial production experience a plus.

Desirable qualifications

• ISO 13485 experience
• Knowledge of Lean Six Sigma manufacturing methods.
• Medical device manufacturing experience

Work Hours

Employees are generally scheduled to work five eight-hour days in a seven-day payroll period. Work days and hours may vary depending upon operational needs. Occasional overtime and weekend work is required.

Key Competencies

• Fluent in Microsoft Office Software.
• Effective communication skills, both verbal and written.
• Excellent organizational skills.
• Possess strong ability to perform detailed repetitive tasks with precision.

Physical Functions

• Approximately 25% of the workdays are spent sitting (e.g. data entry, meetings, filling out forms and checklists, etc.)
• Approximately 75% of the workdays are spent walking or standing (e.g. traveling to and from work areas, etc.)
• Frequent handling, lifting, carrying, pulling, pushing, reaching and grasping performed.
• Ability to lift up to 50 pounds
• Regular stooping, kneeling or crouching.
• Regularly converses with supervisors, co-workers, operators, technicians, management personnel and others to communicate necessary work related information.
• Occasional climbing of stairs, ladders.
• Specific vision abilities required by this job include close vision and color vision.
• Ability to wear a respirator

Key Accountabilities

• Performs chemical and physical testing of aqueous media and pre-polymer batches prior to release of materials for production; as well as, post processing testing of finished goods in accordance with customer and internal sampling plans.
• Performs incoming raw material inspections to check for compliance with company specifications
• Performs validation and RMEP testing as required.
• Performs instrument calibrations as required.
• Maintains and reviews quality documents for accuracy and compliance with ISO standards and ensure availability at point of use.
• Performs the storage and retrieval of retained product samples.
• Routinely makes observations of the pre-polymer and foam line production processes. Reports non-conforming findings to the supervisor.
• Monitors changes to standard operating procedures and make recommendations for improvements to those processes.
• Prepares required product certificates for and assists with final product verifications prior to shipment.
• Interfaces with internal staff to resolve quality system issues and complaints.
• Performs internal audits of other departments.
• Creates/generates standard and ad hoc reports regarding product quality.
• Supports the effort to implement best practices within job scope; expected to participate in activities designed to improve production, quality and Environmental Health and safety (EHS).
• Performs other duties as assigned by supervisor/manager.

Key Decisions

• Determines product conformance to customer specifications.
• Evaluates procedures for clarity and process flow and makes change recommendations.
• Determines if incoming raw materials meet specifications.

Our approach to diversity and inclusion

We strive to have a diverse mix of people from different cultures, ages, geographies and genders, to reflect the world in which we operate and to facilitate innovative thinking across the business

About Mölnlycke

Mölnlycke is a world-leading medical products and solutions company that equips healthcare professionals to achieve the best patient, clinical and economic outcomes.

Our business is organized into four business areas Wound Care, Operating Room Solutions, Gloves and Antiseptics. Customer centricity, sustainability and digitalization are at the heart of everything we do.

Mölnlycke employs around 8,400 people. The company headquarters are in Gothenburg, Sweden and we operate in more than 100 countries worldwide. Since 2007, the company has been part of Investor AB, an engaged owner of highquality, global companies which was founded by the Wallenberg family in 1916. For more information, please visit www.molnlycke.com and