Formulations Associate I, 1st Shift – Drug Product

PCI TRGR Penn Pharmaceutical Services Ltd; San Diego (CA); Hybrid; USD 30,000 - 33,000; Full time

Benefits offered by this job

Health insurance

Dental and vision insurance

401(k) plan

Flexible spending account

Job summary

PCI Pharma Services in San Diego, CA is hiring for a Drug Product Manufacturing Associate I - Formulations (1st Shift). You will support sterile filtration, formulation, in‑process testing, and component preparation in a cGMP environment, under SOPs and batch records.

You’ll assist with schedule adherence and collaborate with the team to resolve technical issues. The role requires a High School Diploma (life sciences preferred) and 0–2 years of manufacturing or lab experience, with strong

Qualifications

• High School Diploma required; life sciences degree preferred.
• 0–2 years manufacturing or lab experience.
• Detail oriented with strong written and verbal communication.
• Familiarity with cGMP, manufacturing, and data entry.
• Proficient with Microsoft Office applications.

Responsibilities

• Perform manufacturing tasks including sterile filtration, formulation, in‑process testing, and component prep.
• Support implementation of procedures and production schedules; assist with master batch records and SOPs.
• Operate production equipment (e.g., TFF, Rotavap, CIP) and maintain qualification for aseptic operations.
• Document, review, and ensure accuracy of batch records; prepare materials for sterilization.
• Collaborate with team on troubleshooting and liaise with Production Planner to obtain materials.

Skills

Detail oriented

Written and verbal communication

Team player

MS Office

QAD knowledge

Education

High School Diploma

Bachelor’s degree in life sciences (preferred)

Tools

MS Office

QAD

Job description

PCI Pharma Services in San Diego, CA is hiring for a Drug Product Manufacturing Associate I - Formulations (1st Shift). You will support sterile filtration, formulation, in‑process testing, and component preparation in a cGMP environment, under SOPs and batch records.

You’ll assist with schedule adherence and collaborate with the team to resolve technical issues. The role requires a High School Diploma (life sciences preferred) and 0–2 years of manufacturing or lab experience, with strong