QC Associate I, Microbiology

Bora Biologics; San Diego (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

Bora Biologics in San Diego is seeking a Quality Control Associate I, Microbiology to perform routine environmental and utilities monitoring of cGMP manufacturing facilities, and to conduct microbiological and chemical testing including endotoxin, bioburden, TOC, and conductivity for product release and compliance.

You will assist with data trending, support method validation activities, contribute to protocols, reports, and SOPs, and report results in a timely, compliant manner while

Qualifications

• BS or advanced degree in a related scientific discipline.
• 0–2 years of progressively responsible experience in pharmaceutical or biologics environments.

Responsibilities

• Conduct Bioburden and endotoxin testing of in-process and product samples.
• Perform environmental monitoring (EM) of classified cleanrooms and controlled areas.
• Collect and test water samples from purified water and WFI systems.
• Maintain accurate and compliant documentation in accordance with cGMP, GDP, and internal SOPs.
• Assist in investigations of microbiological deviations and support CAPA implementation.
• Collaborate cross-functionally with Manufacturing, QA, and Validation teams.
• Perform sample management functions, such as receiving, logging, tracking, storing, and disposal of samples in accordance with SOPs and regulatory requirements.

Skills

Attention to detail

Written communication

Verbal communication

Organizational skills

Problem solving

Regulatory compliance

Team collaboration

Independent work

Education

BS or advanced degree in a related scientific discipline

Tools

Microsoft Office

Job description

Summary

The Quality Control Associate I, Microbiology is responsible for performing routine environmental and utilities monitoring of the cGMP manufacturing facilities. Conducts microbiological and chemical testing including endotoxin, bioburden, total organic carbon (TOC), and conductivity to support product release and facility compliance. Additional responsibilities include assisting with data trending, supporting method validation activities, and contributing to the drafting of protocols, reports, and SOPs related to microbiological operations. The role also involves timely and compliant reporting of test results and participation in investigations as needed.

Job Responsibilities

Essential Functions

• Conduct Bioburden and endotoxin testing of in-process and products samples.


• Perform environmental monitoring (EM) of classified cleanrooms and controlled areas.


• Collect and test water samples from purified water and WFI systems.


• Maintain accurate and compliant documentation in accordance with cGMP, GDP, and internal SOPs.


• Assist in investigations of microbiological deviations and support CAPA implementation.


• Collaborate cross-functionally with Manufacturing, QA, and Validation teams.


• Perform sample management functions, such as receiving, logging, tracking, storing, and disposal of samples in accordance with SOPs and regulatory requirements.

Supplemental Functions

• Other duties as assigned.

Education and Experience

• BS or advanced degree in a related scientific discipline, or equivalent combination of education and experience.


• BS with 0-2 years of progressively responsible experience in pharmaceutical or biologics production environments, or equivalent combination of education and experience.

Knowledge, Skills, and Abilities

• Working knowledge of GLP and cGMP regulations 21 CFR Part 11, 210, 211, 600 & EU guidelines and good documentation practices.


• Knowledge of standard laboratory equipment.


• Basic understanding of microbiological techniques, aseptic practices, and laboratory safety.


• Good organizational and problem-solving skills.


• Ability to follow written procedures and work in a regulated environment.


• Must always adhere to good documentation practices.


• Detail oriented with strong written and verbal communication skills.


• Ability to work independently, within prescribed guidelines, or as a team member.


• Willingness to work in cleanroom settings and handle biohazardous materials under proper PPE and gowning protocols.


• Experience with Microsoft suite (e.g. PowerPoint, Word, and Excel).