1d:I[34901,["/_next/static/chunks/1q_xs299ft_73.js","/_next/static/chunks/1hsg494-jz4os.js","/_next/static/chunks/1zxhbpwnpkk6f.js","/_next/static/chunks/08v7mhpebw2l_.js"],"JobTable"] 1e:T1d11,

About this opportunity:

At Freenome, we are seeking an Inventory Specialist I (Contractor) to help grow the Inventory Operations team. The ideal candidate will work directly with our scientists and partners in Operations, Supply Chain, and Finance to receive, store, track, and distribute materials that support R&D laboratory, clinical, and commercial operations. You are passionate about accurate inventory management, dependable service, and maintaining organized, and compliant workflows. In this role, you will help support Freenome’s mission to change the landscape of cancer detection.

The role reports to the Manager, Inventory Operations. This role will be an onsite role based in our Brisbane, California headquarters and offsite warehouse in South San Francisco, California.

What you’ll do:

Receive and process inbound materials to support Commercial, Clinical and R&D Operations.
Prepare and ship outbound materials in accordance with DOT regulations.
Maintain and follow Inventory controls and procedures to ensure compliance with Clinical Lab Procedures and SOX regulations.
Maintain good record keeping of physical/virtual records of all inbound and outbound material.
Perform inventory cycle counts on a regular cadence to ensure inventory accuracy.
Accurately enter data and perform inventory transactions with the ERP system with a high level of detail.
Review expiration reports, segregate or quarantine expired materials, and coordinate their disposition.
Review inventory requests and fulfill materials for R&D studies and Commercial Production.
Ensure material availability in all laboratory, stockroom and warehouse locations.
Assist in support tasks, projects and initiatives to keep inventory locations secured, organized, and supplied.
Comply with all company, environmental, health and safety policies and procedures.
Perform other duties as assigned.

Must haves:

High School Diploma or GED equivalent.
Ability to load and drive a cargo van to distribute materials across the Freenome campus, clean driving record required.
Ability to safely operate a forklift (training/certification provided).
Min. 1+ years working experience in inventory management and warehouse operations, preferably within a regulated industry.
Ability to lift, push, pull up to 50lbs and stand/walk for long periods of time.
Proficiency execute transactions within an ERP, NetSuite preferred.
Demonstrate strong organizational skills with a attention to detail.
Capability to manage multiple workflows and competing priorities while exercising good business judgment.
Excellent verbal and written communication skills Proficient with Microsoft Office Suites (Word, Excel, PowerPoint); preferable Google Suites.
Ability and willingness to adapt in a dynamic environment and cross train across different warehouse and inventory functions.
Must be able to work outside of the regular business hours to help support the goals of Freenome. This role would have a regular schedule of Tuesday through Saturday. Occasional weekend and overtime may be required.

Nice to haves:

Experience with ISO 13485 and/or CLIA requirements preferred.
DOT shipping certification or familiarity with IATA or 49 CFR requirements preferred.
Forklift Certification or experience preferred.

Additional information:

Contractors may be hired through a third-party provider and will be considered contingent workers. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information.

Freenome is proud to be an equal opportunity employer and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Applicants have rights under Federal Employment Laws.

California applicants please review the CCPA Notice at Collection here:

California Consumer Privacy Act (CCPA)

#LI-ONSITE

1f:T163f,

About this opportunity:

At Freenome, we are seeking a Quality Control Specialist I to help grow the Quality Control team within the Lab Operations Department. The ideal candidate is experienced in Next-Generation Sequencing (NGS) workflows, detail-orientated, and familiar working within a CLIA laboratory setting. This person will perform reagent quality control testing, author and maintain documentation, support method tech transfer, and perform tracking and trending of QC data. You are passionate about contributing to developing life-saving diagnostics through early cancer detection, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer.

The role reports to the Quality Control Supervisor. This role will be an onsite role based in our Brisbane, California headquarters.

What you’ll do:

Perform reagent quality control testing per Standard Operating Procedures
Author, review, and maintain documentation, such as Standard Operating Procedures, Work Instructions, QC Records and Forms for regulatory compliance
Initiate non-conformances for any process deviations or reagent quality control failures
Participate in the investigation of reagent and consumable quality issues
Record, analyze, and trend QC data using good documentation practices
Support the tech transfer and validation of QC test methods to GMP standards
Build and maintain strong knowledge of fundamentals and regulatory requirements applicable to laboratory operations and quality control

Must haves:

Bachelor’s degree in Chemistry, Biochemistry, Biology, Bioengineering or similar field
Ability to follow written procedures and work in a regulated environment
Ability to complete documentation in an accurate and timely manner in order to maintain regulatory compliance
Strong attention to detail and time management skills
Excellent interpersonal and communications skills in order to work in a highly cross-functional environment

Nice to haves:

Experience with performing routine laboratory equipment maintenance
Hands-on experience with automated liquid handlers (e.g., Hamilton, Bravo)
Proficiency with Microsoft Excel, Word, and PowerPoint

Additional information:

Applicants have rights under Federal Employment Laws.

California applicants please review the CCPA Notice at Collection here:

California Consumer Privacy Act (CCPA)

#LI-ONSITE

20:T1872,

About this opportunity:

At Freenome, we are seeking a Quality Control Specialist II to help grow the Quality Control team within the Lab Operations Department. The ideal candidate is experienced in Next-Generation Sequencing (NGS) workflows, detail-orientated, and familiar working within a CLIA laboratory setting. This person will perform reagent quality control testing, author and maintain documentation, support method tech transfer, and perform tracking and trending of QC data. You are passionate about contributing to developing life-saving diagnostics through early cancer detection, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer.

The role reports to the Quality Control Supervisor. This role will be an onsite role based in our Brisbane, California headquarters.

What you’ll do:

Perform reagent quality control testing per Standard Operating Procedures
Author, review, and maintain documentation, such as Standard Operating Procedures, Work Instructions, QC Records and Forms for regulatory compliance
Initiate non-conformances for any process deviations or reagent quality control failures
Participate in the investigation of reagent and consumable quality issues
Record, analyze, and trend QC data using good documentation practices
Support the tech transfer and validation of QC test methods to GMP standards
Build and maintain strong knowledge of fundamentals and regulatory requirements applicable to laboratory operations and quality control

Must haves:

Bachelor’s degree with at least two years of working experience or Master’s degree in Chemistry, Biochemistry, Biology, Bioengineering or similar field
Knowledge of/experience with Quality Control and Quality Assurance principles, including GMP/ISO
Technical writing experience, including Standard Operating Procedures, Work Instructions, QC Records and Forms
Hands-on experience with automated liquid handlers (e.g., Hamilton, Bravo)
Experience with performing routine laboratory equipment maintenance
Exceptional attention to detail and commitment to producing high-quality data
Excellent interpersonal and communications skills, and proven ability to work with team members in the same and adjacent disciplines

Nice to haves:

Experience maintaining 5S workplace organization principles in a laboratory
Experience with softwares such as LIMS, Netsuite, Softmax Pro, and Bartender
Proficiency with Microsoft Excel, Word, and data analysis tools

Additional information:

Applicants have rights under Federal Employment Laws.

California applicants please review the CCPA Notice at Collection here:

California Consumer Privacy Act (CCPA)

#LI-ONSITE

21:T1605,

About this opportunity:

At Freenome, we are seeking a Contract Clinical Research Associate to help grow the Freenome Clinical Development team. The ideal candidate is well-organized, an excellent communicator and experienced in diagnostics clinical trial management. This person is responsible for all things related to assigned aspects of clinical trial monitoring and site management. You are passionate about clinical research, attention to detail and Good Clinical Practice, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer.

The role reports to the Director of Clinical Operations, Dennis McHugh. This role will be a Remote role with occasional travel, as required, to our Brisbane, California headquarters.

What you’ll do:

Ensure compliance with standard protocol and regulatory and ICH GCP obligations in assigned aspects of clinical site monitoring, such as site initiation, routine monitoring, maintenance of study files, study close out, and retrieval of study materials.
Complete on-site and remote monitoring activities in compliance with the Clinical Monitoring Plan, including source document verification for accuracy and integrity, as required.
Write and submit reports of investigational site findings and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate.

Must haves:

Minimum Bachelor’s degree in a life science-related field, a registered nurse (RN) certification, or equivalent.
3+ years’ experience in a clinical trials research environment required, with specific in vitro diagnostics study experience.
General knowledge of regulatory requirements & GCP.
Ability to multi-task, deal with shifting priorities, and proactively solve problems/manage risks.
Strong interpersonal, collaborative, and time management abilities.
Excellent organizational skills; accurate and detail-oriented.
High proficiency in Veeva Vault and Medrio.
Strong spoken and written communication skills.

Nice to haves:

CRA certification by recognized professional organization is a plus, but not mandatory.
Previous experience in the cancer early detection space.

Additional information:

Applicants have rights under Federal Employment Laws.

California applicants please review the CCPA Notice at Collection here:

California Consumer Privacy Act (CCPA)

#LI-REMOTE

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Role	Company	Location	Season	Posted
Inventory Specialist I (Contractor)	Freenome	Brisbane, CA, United States	—	7 days ago
Quality Control Specialist I (Contractor)	Freenome	Brisbane, CA, United States	—	8 days ago
Quality Control Specialist II (Contractor)	Freenome	Brisbane, CA, United States	—	8 days ago
Clinical Research Associate (Contractor)	Freenome	RemoteRemote	—	7 months ago