Ossium
Quality Assurance Specialist, Product Quality
Indianapolis, Indiana, United States
About Ossium Ossium’s mission is to improve the health, vitality, and longevity of human beings through bioengineering. We develop, manufacture, and bank cell therapy products that apply the power of stem cell science to revolutionize treatment for patients with blood, immune, and orthopedic diseases. At Ossium, we empower our employees, maintain the highest standards of operational excellence, and are a force for good.
About the Job We’re hiring a Quality Assurance Specialist to focus on Product Quality and uphold compliance with internal/external standards, regulations, policies, and procedures. This individual will review production and testing records related to the production of bone marrow and bone marrow derived products, ultimately signing off on the Quality Assurance (QA) release of the product for clinical applications. In this role, you will work closely with other departments to identify deficiencies, deviations, and improvement opportunities. Additionally, you’ll be responsible for the execution and monitoring of various quality systems as well as assisting in the development and modification of internal systems to ensure that Ossium products maintain the highest standards of quality and safety.
This position reports to our Associate Supervisor, Product Quality.
Required Qualifications
Associates degree in Life Sciences/Chemistry and 5+ years of experience in Quality
Ability to complete tasks and projects with little oversight
Capable of effectively assimilating information from visual inspection, written documents, and verbal inputs and identifying potential compliance risks
High level of professionalism and good judgmentli>
Excellent written and oral communication skills
Capability to operate with a high level of organization and excellent time management in a dynamic startup environment
This position is based on site in our Indianapolis office; employees will report to Ossium’s facility Monday through Thursday and have the option to work remotely on Fridays
Preferred Qualifications
Bachelor's Degree in Life Sciences/Chemistry
Experience in tissue, organ or cell industry
Understanding of 21 CFR 210, 21 CFR 211, 21 CFR 1271, AATB Standards, and other GMP requirements
Familiarity with and previous experience working with Master Control, preferably in the Production Records module
Key Responsibilities
Review technical production and testing records and identify deviations, non-conformances, and compliance issues
Work across departments to resolve issues and implement improvements
Coordinate and communicate effectively with impacted stakeholders
Sign off on QA release of product for clinical applications
Review and approve Master Batch Records, validations, and other related documents
Promote a culture of quality and continuous improvement through actions and education
Track and trend data related to product quality
Support audits as needed
In your first six months some projects you’ll work on include:
Review Production and Quality Control records and work with the departments to correct errors
Perform the QA release of clinical product so that it can be used as a life-saving treatment
Review and approve Production and Quality Control procedures, validations, and Master Batch Records within the document control system
Learn about Production and Quality Control activities to identify areas of improvement
Physical Requirements
Reporting to Ossium’s facility during regular business hours
Consistently adhering to Ossium’s safety protocols, including wearing appropriate PPE
Moderately noisy open-office environment
Must be able to sit or stand for long periods of time
We offer a full slate of employee benefits including:
Stock options
401(k) matching
Medical, dental and vision coverage
Four weeks of PTO accrued (vacation & sick time) annually + 11 company holidays
Employer paid life insurance and long term disability
Gym membership/recreational sports reimbursements
Ossium Health provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, sexual orientation, gender identity, gender expression, or any other protected characteristic. Our Equal Employment Opportunity Policy Statement and the Know Your Rights: Workplace Discrimination is Illegal Poster reaffirm this commitment. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. If reasonable accommodation is needed, please contact our People Team at careers@ossiumhealth.com or 650-285-0603. Ossium Health complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities.
#J-18808-Ljbffr
About Ossium Ossium’s mission is to improve the health, vitality, and longevity of human beings through bioengineering. We develop, manufacture, and bank cell therapy products that apply the power of stem cell science to revolutionize treatment for patients with blood, immune, and orthopedic diseases. At Ossium, we empower our employees, maintain the highest standards of operational excellence, and are a force for good.
About the Job We’re hiring a Quality Assurance Specialist to focus on Product Quality and uphold compliance with internal/external standards, regulations, policies, and procedures. This individual will review production and testing records related to the production of bone marrow and bone marrow derived products, ultimately signing off on the Quality Assurance (QA) release of the product for clinical applications. In this role, you will work closely with other departments to identify deficiencies, deviations, and improvement opportunities. Additionally, you’ll be responsible for the execution and monitoring of various quality systems as well as assisting in the development and modification of internal systems to ensure that Ossium products maintain the highest standards of quality and safety.
This position reports to our Associate Supervisor, Product Quality.
Required Qualifications
Associates degree in Life Sciences/Chemistry and 5+ years of experience in Quality
Ability to complete tasks and projects with little oversight
Capable of effectively assimilating information from visual inspection, written documents, and verbal inputs and identifying potential compliance risks
High level of professionalism and good judgmentli>
Excellent written and oral communication skills
Capability to operate with a high level of organization and excellent time management in a dynamic startup environment
This position is based on site in our Indianapolis office; employees will report to Ossium’s facility Monday through Thursday and have the option to work remotely on Fridays
Preferred Qualifications
Bachelor's Degree in Life Sciences/Chemistry
Experience in tissue, organ or cell industry
Understanding of 21 CFR 210, 21 CFR 211, 21 CFR 1271, AATB Standards, and other GMP requirements
Familiarity with and previous experience working with Master Control, preferably in the Production Records module
Key Responsibilities
Review technical production and testing records and identify deviations, non-conformances, and compliance issues
Work across departments to resolve issues and implement improvements
Coordinate and communicate effectively with impacted stakeholders
Sign off on QA release of product for clinical applications
Review and approve Master Batch Records, validations, and other related documents
Promote a culture of quality and continuous improvement through actions and education
Track and trend data related to product quality
Support audits as needed
In your first six months some projects you’ll work on include:
Review Production and Quality Control records and work with the departments to correct errors
Perform the QA release of clinical product so that it can be used as a life-saving treatment
Review and approve Production and Quality Control procedures, validations, and Master Batch Records within the document control system
Learn about Production and Quality Control activities to identify areas of improvement
Physical Requirements
Reporting to Ossium’s facility during regular business hours
Consistently adhering to Ossium’s safety protocols, including wearing appropriate PPE
Moderately noisy open-office environment
Must be able to sit or stand for long periods of time
We offer a full slate of employee benefits including:
Stock options
401(k) matching
Medical, dental and vision coverage
Four weeks of PTO accrued (vacation & sick time) annually + 11 company holidays
Employer paid life insurance and long term disability
Gym membership/recreational sports reimbursements
Ossium Health provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, sexual orientation, gender identity, gender expression, or any other protected characteristic. Our Equal Employment Opportunity Policy Statement and the Know Your Rights: Workplace Discrimination is Illegal Poster reaffirm this commitment. Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. If reasonable accommodation is needed, please contact our People Team at careers@ossiumhealth.com or 650-285-0603. Ossium Health complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities.
#J-18808-Ljbffr