What are the responsibilities and job description for the Quality Assurance/Regulatory Affairs Specialist I position at MMQCI?
The Quality Assurance/Regulatory Affairs Specialist I is responsible for activities involving quality assurance and compliance with applicable regulatory requirements. Under the supervision of the Manager of QA/RA, the QA/RA Specialist I is responsible for the maintenance of policies, and management of procedures, that ensure quality compliance to MMQCI’s Quality System, based on federal Quality System Regulation 21CFR820. The successful candidate is experienced in using and maintaining a Quality System according to 21CFR820. It is expected that the QA/RA Specialist I will rapidly develop sufficient expertise to function independently. Maine Molecular is looking for the person with the energy and experience to step into this vital position in a growing company and grow along with us. We have found that our most effective collaboration and creative output stem from daily in-person interactions. As such, this role requires a full-time presence at our office in Saco, ME, and remote work is not an option for this position.
RESPONSIBILITIES:
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 have a beautiful, state-of-the-art facility located in Saco, right next to the Eastern Trail. Come join us!
NO RECRUITERS PLEASE
RESPONSIBILITIES:
- Maintains MMQCI Quality System documentation to ensure compliance with established procedures and regulatory compliance requirements, including, but not limited to, Standard Operating Procedures (SOPs), Master Batch Records, Change Orders, Material Review Notices (MRNs) and Corrective and Preventive Actions (CAPAs).
- Works closely with Manufacturing to support and document MRNs and CAPAs.
- Assists or performs internal audits and supplier audits.
- Supports FDA and customer audits.
- Assists in the assembly Device Master Records for new products.
- Maintains training documentation of all MMQCI employees.
- Must be a nonsmoker due to product contamination prevention requirements.
- Bachelor of Science degree in Life Sciences
- At least 5 years of employment in a cGMP regulated facility
- At least 2 years of experience in Quality Assurance.
- Good communication skills, written and oral, with excellent computer skills including Excel.
- Excellent proof-reading skills
- Very detail oriented.
- Knowledge of current GMP regulations
- Knowledge of ISO 13485 is preferred.
- Experience in laboratory medicine is highly preferred.
- Ability to multi-task in a dynamic environment with changing priorities.
- Strong work ethic.
- Ability to meet challenging timelines, in spite of obstacles.
- Willingness to learn and pitch in as part of team
- Ability to communicate clearly and constructively to correct non-conforming behaviors and practices.
- Medical insurance
- Dental insurance
- 401(k)
- Profit sharing plan
- Vacation
- Holidays
- Sick leave
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 have a beautiful, state-of-the-art facility located in Saco, right next to the Eastern Trail. Come join us!
NO RECRUITERS PLEASE
