iota Biosciences, a wholly-owned subsidiary of Astellas Pharma US, is a medical device company pioneering bioelectronic solutions across a range of medical therapies and diagnostics. Bioelectronic medical implants are the start of an entirely new form of medicine, treating chronic diseases through non-pharmaceutical mechanisms not previously accessible to clinicians.

iota Biosciences, Inc. was acquired by Astellas Pharma US in November 2020. Astellas Pharma US, Inc. is an affiliate of Tokyo-based Astellas Pharma Inc., a top 20 global pharmaceutical research company. Astellas is committed to turning innovative science into medical solutions that bring value and hope to patients and their families. iota’s core proprietary technology stack leverages ultrasonic energy to communicate with and power custom implantable devices, enabling completely new clinical approaches to treating diseases. At iota Biosciences you will be given the opportunity to substantially influence the design and success of these pioneering Class III medical implants, as the company expands the reach of its novel technology while bringing new solutions to the clinic.

We are looking for a Document Control Specialist who is highly motivated and passionate to manage quality system and product supporting documentation for novel Class III active implantable devices.

The Document Control Specialist will be expected to:

• Serve as the Document Control reviewer and/or approver, ensuring documents/records and changes comply with established procedures and requirements, and ensuring change elements are identified, compliant, and assembled for review and approval

• Promptly process Document/Engineering Change Requests and Change Orders (DCR, DCO, ECR, ECO) in compliance with Document and Record Control processes

• Ensure appropriate functional area representatives are involved in review and/or approval

• Process and archive paper and electronic quality records; review for compliance to applicable standards

• Implement employee training on documents, SOPs, and procedures

• Track, manage and report training compliance on continuous basis

• Coordinate new hire onboarding processes as related to the QMS

• Deliver change control data, reports, and information upon request

• Deliver Regulatory submission requests for documentation upon request

• Assist in projects for continuous improvement of the eQMS

Qualifications:

• Bachelor's degree

• Minimum two years of relevant experience, preferably in a Quality function in the Medical Device or regulated industry

• Organized, self-motivated, ability to effectively manage multiple projects and priorities; high attention to detail

• Effective interpersonal and communication and writing skills

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At iota Biosciences, we take pride in providing equal employment opportunities to everyone, inclusive of race, ethnicity, beliefs, religion, marital status, gender, gender identity, citizenship status, age, veteran status or disability.

iota offers a very competitive benefits package that includes the following:

Health

Employees thrive when healthy, both physically and mentally:

Comprehensive health coverage for you and your family, covered at 100%

Employee Assistance Program

Time-off

Take time off when you need to take it:

Generous PTO policy

Paid parental leave

Paid holidays beyond the traditional

Paid volunteer day

Competitive Compensation

In addition to our competitive base salaries, we offer:

Annual Bonus Plan

Long Term Incentive Plan (LTIP)

401k plan with matching contributions equal to 100% of your deferral contributions up to 5% of your eligible compensation