Looking for a career that matters?
Join Mölnlycke! We design, manufacture, and supply medical solutions that enhance performance in healthcare worldwide. We’re looking for people who are passionate about helping others and work well in a team-based environment.
Mölnlycke, a medical device manufacturer in Brunswick, ME, is seeking full-time Quality Assurance Technician for our Weekend Shift (6:00AM-6:00PM). To support our manufacturing of healthcare products worldwide. We are looking for people who are passionate about helping others and work well in a team based environment.
What we offer:
Entry-level position with comprehensive, on-the-job paid training
The pay rate for this role is $23.89 an hour to start $2.00 shift differential between the hours of 5:30pm to 5:30am PAID BREAKS!!!! Consistent raises and opportunities for growth in our new tier-pay model.
Work schedule: Friday, Saturday and Sunday 6:00am – 6:00pm Workdays and hours may vary depending on operational needs; occasional overtime and weekend work may be required
Our comprehensive benefits package is designed to support your health, financial well-being, and work-life harmony.
Medical, dental and vision plans are available from your first day of employment, and provide extensive coverage through multiple options so you can find the right fit for you and your family. Financial benefits include a robust 401(k) plan with company match, profit sharing, tuition reimbursement, life insurance and both flexible spending accounts and health savings accounts. Molnlycke offers Generous Paid Time Off (accrual equal to 3 weeks a year) 11 Paid Holidays 4 Weeks Paid Parental Leave An Employee Assistance Program Lifestyle Perks like discounted access to entertainment and travel
Here’s a snapshot of what you’ll do:
The Quality Assurance Technician is responsible for monitoring the quality of manufactured wound care products and ensuring the quality system is operating according to regulatory requirements and ISO standards.
Testing and verification of manufactured products, includes ensuring product conformance to specifications by conducting physical testing in a controlled laboratory environment in preparation for sterilization and final release.
QMS system operation includes maintaining specific subsystems as assigned by the QA Supervisor such as CAPA, Document Control, Internal Auditing and Supplier Quality. Other duties may include development and implementation of new procedures, standards and specifications as required by the Quality Management System.
Performs physical testing of finished goods in accordance with product specifications and internal sampling plans. Performs incoming raw material inspections to check for compliance with company specifications. Performs validation material testing as required. Performs data mining activities for trend analysis and improvement projects. Tracks instrument calibrations and ensure test equipment is maintained as required by the calibration schedule. Maintains and reviews quality documents for accuracy and compliance with regulatory requirements and ISO standards. Manages the storage and retrieval of retained product samples. Routinely makes observations of production line 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 release documents and assists with final product verifications prior to shipment. Interfaces with other departmental staff members to resolve quality system issues and complaints. Conducts internal auditing of quality system processes. 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 EHS.
What you’ll need:
Pre-employment physical, background check, and at least 2 professional references required Proven success working in a team-based environment as well as the ability to meet performance measures with minimal direct supervision and guidance Ability to make well-reasoned decisions both independently and as part of a team Effective communication and organization skills Basic mechanical, mathematical, and computer skills (MS Word, Excel, Access, and Outlook) Ability to work overtime to ensure production goals are met Over 75% of the workdays are spent walking or standing Ability to lift up to 50 pounds Regular handling, lifting, carrying, pulling, pushing, reaching, and grasping Close vision and color vision are required Ability to wear a respirator Experience in production, manufacturing or related environment preferred, but not required.
PLEASE NOTE: This position's functional demands require working around or near equipment that may be hazardous to individuals with pacemaker equipment.
Our approach to diversity and inclusion
At Molnlycke, diversity is not just a vision, but our strength. We are dedicated to fostering an inclusive workplace that values and celebrates the power of diversity. At the heart of our commitment is the belief that diversity fuels innovation, creativity, and problem-solving. We invite you to be a part of a team where authenticity is embraced and every employee, regardless of background or any other traits, experiences a true sense of belonging. Your attitude, drive, enthusiasm, and eagerness to learn are just as important to us as the requirements for the role.
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 high-quality, global companies which was founded by the Wallenberg family in 1916. For more information, please visit www.molnlycke.com and www.molnlycke.com/careers
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Information at a Glance #body.unify div.unify-button-container .unify-apply-now:focus, #body.unify div.unify-button-container .unify-apply-now:hover{color:rgb(255,255,255) !important;}#body.unify div.unify-button-container .unify-apply-now:focus, #body.unify div.unify-button-container .unify-apply-now:hover{background:rgba(2,95,58,1.0) !important;} Apply now Req ID: 7975 Posting Start Date: 25/09/2024 Working Location: Office Category: Quality and Regulatory Function: COO & Sustainability Job Posting Location: US Brunswick Factory Site