# Title QA Specialist, Drug Substance Manufacturing at Filmore

- Company: Filmore
- What the company does: Backed by 500 Global.
- Company website: https://filmorebody.com
- Type: Startups
- Level: Mid level
- Location: Remote (US)
- Work setup: Remote
- Posted: 2026-11-02
- Apply by: 2026-12-17
- Apply: https://uscareers-fujifilm.icims.com/jobs/39211/qa-specialist%2c-drug-substance-manufacturing/job?utm_source=1752vc&utm_medium=careers
- Page: https://www.1752.vc/careers/jobs/filmore-title-qa-specialist-drug-substance-manufacturing/

## About the role

The QA Specialist, Drug Substance Manufacturing (DSM) is responsible for partnering in the Quality oversight of Drug Substance Manufacturing processes. This role provides oversight of validation program execution for these processes and systems to ensure applicable DSM systems and processes are operated/maintained in a validated state throughout their lifecycle, with a focus on consistent policy administration. Found on 1752vc Careers, the job board for startup and VC roles.

## What they're looking for

- Strong verbal and written communication skills to partner with different teams and stakeholders
- Strong time management, ability to meet tight deadlines to ensure effective prioritization of tasks
- Basic knowledge and application of cGMP compliance and other related regulations
- Excellent oral and written communications skills and fluency in English
- Understanding of GAMP5, Data Integrity, and application of 21 CFR Part 820 and Part 11 required
- Understanding of cell culture, upstream processes, large scale recovery and/or downstream processes


Source: 1752vc Careers, https://www.1752.vc/careers/jobs/filmore-title-qa-specialist-drug-substance-manufacturing/