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Quality Assurance Specialist

MMQCI

Saco, ME

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Biology, Communication Skills, Compensation and Benefits, Corrective Action, Current Good Manufacturing Practice (cGMP), DNA, Dental Insurance, Detail Oriented, Disease, Documentation, Fishing, GMP (Good Manufacturing Practices), Hospital, ISO (International Organization for Standardization), Infectious Diseases, Insurance Regulations, Internal Audit, Laboratory, Lift/Move 30 Pounds, Maintain Compliance, Microsoft Product Family, Multitasking, Oncology, Pharmacogenetics, Policy Development, Precision Testing, Presentation/Verbal Skills, Product Development, Proofreading, Quality Assurance, Quality Control, Quality Management, Regulations, Regulatory Compliance, Regulatory Reports, Regulatory Requirements, Restaurant, Staff Training, Standard Operating Procedures (SOP), Systems Maintenance, Team Player, Testing, Time Management, Vision Plan, Writing Skills
LOCATION
Saco, ME
POSTED
30+ days ago
Ensure Quality & Compliance as Our Next QA/RA Specialist! 

 The Quality Assurance/Regulatory Affairs Specialist plays a key role in supporting quality assurance activities and ensuring compliance with applicable regulatory requirements. Reporting to the Manager of QA/RA, this position is responsible for maintaining policies and managing procedures that support MMQCI’s Quality System in alignment with ISO 13485 standards. 
The ideal candidate brings experience working within an ISO 13485-regulated environment and is comfortable supporting and maintaining quality systems. This role offers the opportunity to quickly build expertise while working in a collaborative environment. 
 
What You Will Get to Do 
  • Review and approve all Quality Management System documentation (i.e. batch records and QC testing) to ensure compliance with QMS certifications and investigations 
  • Collaborate with departments to investigate Material Review Notifications and develop Corrective and Preventive Action plans 
  • Independently reviews and authorizes process and equipment validations 
  • Performs or assists with audits, including internal, customer, and regulatory audits 
  • Maintains MMQCI’s ISO 13485 certification  
  • Writes SOPs and trains key personnel as needed to support all departments 
  • May be called on to assist others and perform additional tasks as assigned 
 
Required Skills & Experience
  • Bachelor’s degree in Life Sciences with 5+ years’ experience in a cGMP-regulated environment, including at least 2 years in Quality Assurance 
  • Knowledge of current GMP regulations, ISO 13485, and In Vitro Diagnostic Regulation (IVDR) is preferred 
  • Strong written and verbal communication skills; proficient in Microsoft Suite 
  • Excellent proofreading skills with strong attention to detail 
  • Ability to manage multiple priorities in a fast-paced, changing environment and meet challenging deadlines 
  • Strong work ethic, team-oriented mindset, and willingness to learn 
  • Ability to communicate clearly and constructively  
  • Must be able to lift up to 30 lbs  

Why You’ll Love Working Here  
  • Opportunity to make a meaningful impact within a growing diagnostic company 
  • Collaborative, mission-driven team environment 
  • Competitive compensation and benefits 
 
Benefits We Offer 
• Medical, dental, and vision insurance 
• 401(k)                                                                                        
• Profit Sharing Plan 
• Vacation 
• Holidays 
• Sick leave 

Get to know the MMQCI team! 
https://www.mmqci.com/about/employeespotlight/employee-spotlight.html 
 
Maine Molecular Quality Controls, Inc. (MMQCI) designs, develops, manufactures, and 
markets unique quality control products used by hospital laboratories to monitor the accuracy of tests for inherited disease, pharmacogenetics, oncology, and infectious diseases. MMQCI has developed technologies to stabilize DNA and RNA for use as quality controls and continues to pursue the discovery of novel techniques useful for the development of new quality control products.
 
 MMQCI is conveniently located in beautiful southern coastal Maine, minutes from the Maine Turnpike, Portland International Jetport, and less than 2 hours from Boston. Close by are fabulous Portland restaurants, sandy beaches, and a plentiful supply of Maine lobsters! Many terrific outdoor activities are easily accessible including hiking, biking, kayaking, fishing, skiing and snowshoeing. We’re in a state-of-the-art facility, located in Saco, right next to the Eastern Trail. Come join us! 

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MMQCI

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