2nd Shift Formulations Technician – GMP Drug Product

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

Benefits offered by this job

Paid time off

Health insurance (dental & vision)

Flexible spending account

401(k) plan

Job summary

PCI Pharma Services in San Diego, CA is hiring a Drug Product Manufacturing Associate I - Formulations for 2nd shift (2:00 PM–10:30 PM). The role supports routine cGMP manufacturing tasks, sterile formulation, in-process testing, and documentation of batch records in a GMP environment.

The ideal candidate has a high school diploma (life sciences degree preferred), 0–2 years of manufacturing or lab experience, and strong written and verbal communication.

Qualifications

• High School Diploma required; life sciences degree preferred.
• 0–2 years of relevant manufacturing or laboratory experience.
• Detail oriented with strong written and verbal communication skills.
• Ability to work independently, within guidelines, or as part of a team.
• Familiarity with cGMP, manufacturing, machine operations, and data entry.
• Proficient with Microsoft Office applications.

Responsibilities

• Perform sterile filtration, formulation, in-process testing, and preparation of formulation components.
• Support implementation of manufacturing procedures and production schedules.
• Assist colleagues with technical issues during the shift.
• Initiate revisions to Master Batch Records and SOPs.
• Operate production equipment and maintain aseptic GMP environments.
• Document, review, and ensure accuracy of batch records.

Skills

Detail oriented

Written and verbal communication

GMP familiarity

Microsoft Office

Independent worker / team player

Education

High School Diploma

Bachelor’s degree in life sciences

Tools

QAD system

Job description

PCI Pharma Services in San Diego, CA is hiring a Drug Product Manufacturing Associate I - Formulations for 2nd shift (2:00 PM–10:30 PM). The role supports routine cGMP manufacturing tasks, sterile formulation, in-process testing, and documentation of batch records in a GMP environment.

The ideal candidate has a high school diploma (life sciences degree preferred), 0–2 years of manufacturing or lab experience, and strong written and verbal communication.