Quality Assurance Engineering Lead, Industrial Position Available In Polk, Florida
Tallo's Job Summary: Molekule Group, Inc in Lakeland, FL is seeking a full-time Quality Assurance Engineering Lead, Industrial with a salary range of $71.7K - $92.1K a year. The role requires a Bachelor's degree, 3+ years of experience, and skills in Six Sigma Analysis, FDA regulations, and lean manufacturing. Responsibilities include managing supplier audits, quality checks, and developing test protocols for filters and devices.
Job Description
Quality Assurance Engineering Lead, Industrial
MOLEKULE GROUP, INC
Lakeland, FL Job Details Full-time Estimated:
$71.7K – $92.1K a year 1 day ago Benefits Health insurance Dental insurance Vision insurance 401(k) matching Qualifications Mid-level 3 years Six Sigma Analysis skills Bachelor’s degree Organizational skills Quality systems Communication skills Lean manufacturing FDA regulations
Full Job Description Description:
Summary:
Molekule is looking for an on-site Quality Assurance Engineering Lead, Industrial to join our Quality and Regulatory Team. As a QA Engineering Lead, Industrial you will work closely with both the Engineering, Operations and R D teams to ensure that our products are being manufactured with the highest level of quality and detail. A successful candidate thrives in a fast-paced environment, is creative in their approach and is self-motivated.
What You Will Own:
Manage filter and device supplier audits and ensure filter and device elements meet our incoming requirements Manage filter and device assembly CMs – define quality requirements and review KPIs to ensure filter and device meets quality/performance expectations Develop and execute quality test protocols for filters and devices (and filter and device elements) Develop and implement incoming, in process, final and outgoing quality checks to ensure high quality of material being placed into process, high quality process of material and high quality of final product Assist R D and Engineering team in testing, and standards definition, of new filter and device elements / processes Monitor and report filter and device manufacturing yields Manage filter and device related CAPAs, NCMs, etc Identify quality problems and recommend solutions Track and update periodic QA / Document Control metrics and dashboards Report on quality issues and yields, inbound and outbound material specifications, production logs and waste Co-manage document control needs, including the management of ECOs, MCOs Assist the repair team in FA activities for return systems / filters and devices Monitor and report field failure trends for systems / filters and devices Assist customer support teams in defining failure modes and responses to customers Maintain a sense of flexibility in the role as we grow, and possess a willingness to wear multiple hats
Requirements:
What You Will Bring:
Bachelor’s degree in science or related field, preferably Engineering 3+ years in a quality, operations or data analyst role Strong analytical capabilities – knowledge of scientific mathematics and a clear understanding of statistical concepts, SPC, sampling and validation
Pluses:
Experience with consumer electronics Experience with scientific products Experience with textile products or coating processes FDA-specific training or certifications, or experience in regulatory compliance Experience with FDA-cleared medical devices, QMS quality systems Experience working with domestic and international suppliers Knowledge of lean manufacturing and six sigma methodologies Pro-active problem solver with great attention to detail Excellent oral and written communication skills; good organizational skills Experience with Air Quality monitoring (PM, VOC, etc) What’s in it
For You:
Career Growth:
progress and learn, stability, career development/path.
Work Environment:
autonomy, ownership, recognition of achievements, life-work balance (see what we did there), challenges.
Culture:
transparency of goals and plans, support, collaboration, trust, community, passion, growth mindset.
Benefits:
health, dental and vision insurance & more, unlimited discretionary time off (DTO), matching 401K, flexibility (i.e. work day start and end times).
Compensation:
fairness, timeliness, compensation system. We are Molekule and we’re changing air purification. Molekule was created with a goal of using the power of science to eliminate indoor air pollution around the world. Our vision is to change the world from the indoors out by improving the safety and health of the places where we live, conduct business, learn, heal and connect. It’s a lofty goal, but that’s why we need you! Molekule Values – Making Life Easy For Someone Else “For our colleagues, for our customers, and for those who don’t have equitable access.” Say The Hard Thing “We solve problems with empathy and honesty.” Trust The Data “We are guided by science and make decision based on the numbers, even if it means changing our opinion.” Make The Invisible Visible “We reveal and address inefficient and inequitable dynamics at work and in the world.” Push For 1% More “We have a growth mindset and push for positive change every day.” Act As Community “We face challenges together. We celebrate victories together. We share skills together.” Molekule is an Equal Opportunity/Affirmative Action Employer. We will consider employment for qualified applicants with criminal histories in a manner consistent with the requirements of the San Francisco Fair Chance Ordinance. The Company will also not discharge, or in any manner discriminate or retaliate against, any employee who discloses their own wages, discusses the wages of others, inquires about another employee’s wages, or aids or encourages any other employee to do the same. The Company is not obligated to disclose wages unless its State mandated. Applicants with disabilities may e-mail , to request and arrange for accommodations. If you need assistance to accommodate a disability, you may request an accommodation at any time.