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Rose International 2nd Shift Quality Supervisor in Brooklyn Park, Minnesota

Position Title: 2nd Shift Quality Supervisor Position Number: 352926 Location: Brooklyn Park, MN 55428 Position Type: Temporary Required Skill Set: GMP, Medical device, Quality Control Optional Skill Set: Management Position Description: **Only U.S. Citizens and those authorized to work in the U.S. can be considered as W2 candidates.** Job Title: Quality Supervisor (2nd Shift, 3:00pm-1:00am) Requirement Number: 16548 Start date: ASAP Duration or End date: 6 Months Location: Brooklyn Park, MN 55428 Hours: 3:00pm-1:00am 2nd Shift Quality Supervisor Responsible for providing Quality support and oversight via direct staff supervision or process/area responsibilities. Responsible for 2nd shift incoming inspection and finished goods quality inspections. Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and quality practices. Essential Duties and Responsibilities: The incumbent will perform other duties assigned. Leads ongoing, daily departmental operations. May include the supervision of assigned personnel in achieving defined quality goals in an efficient, accurate and timely manner; Interview/hire, evaluate, train and develop direct reports Perform in-depth internal assessments and evaluations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude. Assessments and information gathering may be through in-depth employee interviews, flow charting and other informational gathering techniques. Work closely with production supervisors, quality, engineering and other internal groups to accomplish the above and influence necessary actions. Determine the logic, adequacy and effectiveness of processes, systems and related requirements. Develop plans to correct identified risks including areas of non-conformance. Inform management and implement approved corrective action plans. Serve as Subject Matter Expert (SME) by maintaining a high level of expertise in current regulatory requirements. Provide training and coaching to local employees and others as needed on relevant area(s). When required, assist other Quality areas in the successful performance of these activities. Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc. Participate in external assessments and audits by evaluating and solving product/process problems by providing technical, analytical and supervisory skills Support process with timely closure of observations/audit items. Participate in QA/QC multi-site projects in the role of contributor, coordinator or lead. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Strong interpersonal skills and great attention to detail are necessary. Must be a strong team player with good problem solving, and good verbal and written communication skills. Must have the ability to manage people, encourage teamwork and drive decisions. Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices. Education and/or Experience: BS in engineering/business/science or equivalent. 3-5 years exp. in Quality with a medical device company. Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in