Top 6 Quality assurance specialist Jobs in Maine

Quality Assurance Specialist
MMQCI —Saco, ME
- Full-time
- 5 years
- Bachelor's degree
- Senior level
- Profit sharing
- Paid parental leave
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Temporary Quality Assurance Specialist
HEALTHPLANONE, LLC —West Farmington, ME
- Full-time
- Spanish
- Microsoft Outlook
- Writing skills
- Health insurance
Quick Apply
6d
Quality Control Specialist
Kennebec Savings Bank —Augusta, ME
- $21.40 - $32.66 an hour
- 5 years
- Word processing
- Computer literacy
Quality and Compliance Specialist
3Rivers —Gardiner, ME
- $22 - $25 an hour
- Weekends as needed
- HIPAA
- Mid-level
- Office
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Temporary Quality Assurance Specialist
HEALTHPLANONE, LLC —West Farmington, ME
Evaluates/audits calls and evaluate the quality of each call based on the quality guidelines and standards. Associate degree in business or related field.
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6d

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Quality Assurance Specialist (QAS)
Fox River Associates —Columbus, OH
Auditor certification by accredited body (Certified Quality Engineer/Certified Quality Technician/ISO 9001:2015 Lead Auditor Training).
$60,000 - $65,000 a year
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Quality Specialist
Engineered Profiles LLC —Columbus, OH
Assist in training floor associates on procedures & quality gauges / tools. 401k Retirement Plan- Company matching. Assist in tracking trends or quality issues.
$16.97 - $22.05 an hour
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7d

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Quality Assurance Specialist

MMQCI
Saco, ME

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Job Details

Full-time

Benefits

Profit sharing
Paid parental leave
Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Parental leave
Vision insurance

Qualifications

Bachelor's degree
Editing

Full Job Description

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) retirement savings plan
Company profit sharing program
Paid time off, including vacation, holidays, and sick leave
Paid Parental Leave Program

Get to know the MMQCI team!
https://www.mmqci.com/about/employee-spotlight/employee-spotlight.html

Maine Molecular Quality Controls, Inc. (MMQCI) designs, develops, manufactures, and sells unique quality control products used by hospital laboratories and manufacturers to monitor the accuracy of tests for genetic, oncologic, and infectious diseases. MMQCI has proprietary 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!

Interested in joining our team? Please submit both a resume and cover letter with your application for consideration.

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quality assurance specialist jobs in maine

Quality Assurance Specialist

Temporary Quality Assurance Specialist

Quality Control Specialist

Quality and Compliance Specialist

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