ISO Compliance & Administration Position Available In Shelby, Tennessee

ISO Compliance & Administration Southern Systems International Memphis, TN Job Details Full-time $25 – $28 an hour 22 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance 401(k) matching Qualifications Microsoft Excel ISO standards Spreadsheets Compliance audits & assessments

ISO 9001

Research Mid-level Compliance management Project management Quality assurance Bachelor’s degree Attention to detail Compliance management software Organizational skills Clinical trials 2 years Communication skills FDA regulations Full Job Description Job Summary We are seeking a detail-oriented and proactive ISO Compliance & Administration professional to join our team. This role is essential in ensuring that our organization adheres to ISO standards and regulatory requirements. The ideal candidate will have a strong background in compliance management, quality assurance, and project management, particularly within the context of FDA regulations and chemistry manufacturing controls. You will play a critical role in supporting our clinical trials and maintaining the integrity of our compliance processes. Duties Develop, implement, and maintain ISO compliance programs to meet regulatory standards. Conduct thorough research on FDA regulations and ensure all documentation aligns with current guidelines. Manage projects related to compliance initiatives, ensuring timely completion and adherence to quality standards. Collaborate with cross-functional teams to facilitate compliance training and awareness. Oversee quality assurance processes, including audits and assessments of compliance practices. Maintain accurate records of compliance activities and prepare reports for management review. Support clinical trials by ensuring all necessary documentation meets regulatory requirements. Act as a point of contact for compliance-related inquiries and provide guidance as needed. Requirements Bachelor’s degree in a relevant field such as life sciences, quality assurance, or project management. Proven experience in ISO compliance management or related roles. Strong understanding of FDA regulations and their application within the industry. Familiarity with chemistry manufacturing controls and quality assurance practices. Excellent research skills with the ability to analyze complex regulatory information. Demonstrated project management skills with the ability to manage multiple priorities effectively. Strong attention to detail and organizational skills. Excellent communication skills, both written and verbal, with the ability to work collaboratively across departments. Join us in ensuring that our organization meets the highest standards of quality and compliance. Your expertise will be invaluable in maintaining our commitment to excellence.

Job Type:

Full-time Pay:

$25.00 – $28.00 per hour Expected hours: No less than 40 per week

Benefits:

401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance

Schedule:

Monday to

Friday Work Location:

In person