Manufacturing Investigator I — Deviation & Documentation Lead

PCI TRGR Penn Pharmaceutical Services Ltd; San Diego, Northern (CA, KY); Hybrid; USD 26,000 - 30,000; Full time

Benefits offered by this job

Paid time off

Health insurance

Flexible spending account

401(k) plan

Job summary

PCI Pharma Services in San Diego, CA is seeking a Manufacturing Investigator I under direct supervision to investigate deviations, CAPAs, complaints, and other cGMP documents, supporting cross-functional teams and ensuring timely closure of investigations.

This full-time role requires attention to detail, strong written and verbal English, and proficiency with MS Office as you prepare writeups, track trends, and assist audits in a fast-paced manufacturing setting.

Qualifications

• Bachelor’s or Associate degree preferred; high school diploma or equivalent required.
• 1–2 years of manufacturing experience; cGMP environment preferred.
• Familiarity with GMP documentation (SOPs, deviations, CAPAs) preferred.
• Detail oriented with strong English writing and communication skills.

Responsibilities

• Under direct supervision, investigate deviations, CAPAs, complaints and cGMP documents.
• Coordinate and revise investigations, write-ups and related documentation.
• Support cross-functional teams and review procedures for accuracy.
• Track trends in documentation and assist internal and client audits.
• Maintain a GLP/cGMP environment and adhere to SOPs.
• Ensure timely close-out of batch record revisions and investigations.

Skills

English writing

Verbal communication

Microsoft Office

Attention to detail

Teamwork

Independence

Education

Associate or Bachelor's degree preferred

High school diploma or equivalent required

Job description

PCI Pharma Services in San Diego, CA is seeking a Manufacturing Investigator I under direct supervision to investigate deviations, CAPAs, complaints, and other cGMP documents, supporting cross-functional teams and ensuring timely closure of investigations.

This full-time role requires attention to detail, strong written and verbal English, and proficiency with MS Office as you prepare writeups, track trends, and assist audits in a fast-paced manufacturing setting.