On-Process QA Specialist — Real-Time Quality Oversight

Nivagen Pharmaceuticals; Sacramento (CA); On-site; USD 60,000 - 92,000; Full time

Benefits offered by this job

Yearly bonus eligibility

Medical, dental and vision coverage

Paid time off plan

401k savings plan

Job summary

A leading pharmaceutical company in Sacramento seeks an 'In Process QA Specialist' to ensure pharmaceutical product quality during manufacturing. The candidate will perform real-time monitoring, conduct checks, and collaborate cross-functionally. A Bachelor's degree in a relevant field and up to 3 years of experience in regulated environments are required. The role includes QA oversight within manufacturing areas and documentation review. Competitive pay and benefits with a focus on employee well-being are offered.

Qualifications

• Bachelor’s degree or equivalent in a related field.
• 0–3 years of experience in a regulated manufacturing environment.
• Knowledge of cGMP and FDA regulations.

Responsibilities

• Perform routine QA oversight and ensure compliance with GMP.
• Conduct line clearances and in-process checks.
• Review and approve GMP documentation.

Skills

Strong analytical and problem-solving skills

Attention to detail

Effective communication skills

Ability to work independently and collaboratively

Education

Bachelor’s degree in Life Sciences, Chemistry, Engineering, or related field

Tools

ComplianceWire

TrackWise

SAP

LIMS

Microsoft Office

Job description

A leading pharmaceutical company in Sacramento seeks an 'In Process QA Specialist' to ensure pharmaceutical product quality during manufacturing. The candidate will perform real-time monitoring, conduct checks, and collaborate cross-functionally. A Bachelor's degree in a relevant field and up to 3 years of experience in regulated environments are required. The role includes QA oversight within manufacturing areas and documentation review. Competitive pay and benefits with a focus on employee well-being are offered.