About Soleno Therapeutics Inc

Soleno is a biopharmaceutical company focused on the development and commercialization of novel therapeutics for the treatment of rare diseases based in Redwood City, CA.

At Soleno, we are driven by the unique and multi-faceted needs of the PWS community. Like these individuals, resilience is part of who we are – it is in our chromosomes – and our team is made up of exceptional colleagues whose collective efforts are woven together to deliver meaningful outcomes, both professionally and for those living with PWS. 

We value collaboration, integrity, and respect. These characteristics have allowed us to forge strong, authentic bonds with the caregivers, patients, health care professionals (HCPs) and community members we serve. We are proud to work alongside them every step of the way. 

Our employees are our greatest asset, and we're expanding across functions during this pivotal time. We invite you to join us in making an impact—and making history.We all share the most important goal of bringing solutions to the PWS community. 

Summary of Job (brief description)

We are seeking a highly motivated individual to join Soleno Therapeutics supporting Quality Systems. Responsibilities primarily include the oversight of Soleno’s Document Control and Training Systems.

Responsibilities

• Maintain the GxP Document Control and Training systems.
• Process document change controls and training records.
• Provide formatting support on controlled documents using Microsoft suite (e.g., Word, Excel).
• Maintains hard copy files and electronic files of GxP records.
• Participates in developing and improving Standard Operating Procedures to ensure quality objectives are met.
• Assist in quality systems and compliance activities, including but not limited to supplier quality, audit management, inspection readiness, internal audit, deviations, change controls and CAPAs.
• Foster a quality culture that values innovation, continuous improvement, and personal accountability. Support GxP systems and process improvement initiatives.
• May work on assignments and other duties to support Quality Systems where judgement is required in resolving problems and making recommendations.
• Keeps abreast of requirements for compliance in own area of work. Participates as required in training on regulatory issues affecting own area of work. Notifies Manager of compliance questions and issues.

Qualifications

• Bachelor’s Degree in a scientific discipline.
• Minimum of 3-5 years of relevant experience in Quality (Document Control) in the pharmaceutical/biotech industry or equivalent combination.
• Previous experience using an eQMS system is required.
• Demonstrates proficiency in Microsoft Office suite (e.g., Word, Excel).
• Knowledgeable of current regulatory guidance, including GxPs.
• Demonstrates ability to perform detail-oriented work with a high degree of accuracy.
• Demonstrates excellent verbal, written, and interpersonal communication skills.
• Responsible and self-motivated with effective time management, organizational, and planning skills.

Salary Range: $80,000 - $100,000

(Actual salary at the time of hire may vary and may be above or below the range based on various factors, including, but not limited to, the candidate’s relevant qualifications, skills, and experience, as well as the location where this position may be filled.)