Quality Assurance Associate I

Quality Assurance Associate I at Lumen Bioscience

Lumen Bioscience is seeking a dedicated Quality Assurance (QA) Associate I to assist with maintaining our quality management system. This essential role supports compliance activities related to cGMP, cGLP, and cGCP (cGXP) standards, ensuring high-quality documentation, thorough reviews, and operational adherence to pharmaceutical regulations. If you have a keen eye for detail, excellent organizational skills, and a commitment to quality, we encourage you to apply.

Role Description:

Documentation and Records:   Perform document scanning and archival of controlled records, maintain accurate activity logs, and issue process documentation for manufacturing operations.

Operational Support:   Provide on-the-floor QA support to manufacturing operations, assisting in ensuring compliance with established cGXP processes.

Batch Record Review:   Conduct detailed reviews of batch records and related process documentation to uphold stringent quality standards.

Compliance Walkthroughs:   Regularly conduct facility and operational walkthroughs to verify compliance with the company's quality management system aligned with 21 CFR parts 210/211.

QA Team Support:   Assist the QA Manager and QA Specialist in various quality assurance tasks, including metric report preparation and quality event investigations.

Essential Duties and Responsibilities:

Maintain organized documentation through scanning, archiving, and record-keeping.

Issue and review process documentation associated with manufacturing schedules.

Support on-the-floor quality assurance for manufacturing compliance.

Perform facility walkthroughs to ensure adherence to pharmaceutical regulatory requirements.

Assist with investigations and management of deviations, CAPAs, and other quality-related events.

Support internal and external audits, validation, qualification, and verification activities as needed.

Qualifications & Requirements:

Educational Background:   Associate's degree in a relevant scientific field, or at least 1 year of work experience in a regulated cGXP environment.

Technical Knowledge:   Familiarity with cGMP, ISO 9001, and ICH requirements related to document control and quality records.

Technical Skills:   High proficiency in Microsoft Word, Excel, and SharePoint.

Personal Attributes:   Strong organizational skills, detail-oriented, ability to multitask, excellent communication skills, adaptability, and commitment to quality and ethical standards.

Physical Requirements:

Ability to sit and stand for extended periods (2+ hours each).

Occasionally lift or carry items up to 20 kg.

Salary & Benefits at Lumen Bioscience:

$65,000 - $70,000 annually 

Health, Dental, and Vision premiums fully covered by Lumen.

401k match up to 4%, in addition to annual stock bonuses for all employees.

Industry-leading PTO policy, paid refresh days, and year-end holiday office closure.

Monthly wellness programs to support employee health.

Free onsite parking or public transportation subsidies.

Comprehensive parental leave.

Life insurance, short & long-term disability, and employee assistance programs.

At Lumen Bioscience, we foster a collaborative and innovative work environment where your contributions directly impact biotechnology and global health solutions.

Join us and play a vital role in maintaining exceptional quality standards and regulatory compliance.

Compensation Range

$65,000 — $70,000 USD