Senior Biopharma Automation Engineer

PCI TRGR Penn Pharmaceutical Services Ltd; San Diego (CA); On-site; USD 107,000 - 120,000; Full time

Benefits offered by this job

Paid time off

Health insurance (including dental &視)

Flexible spending account

401(k)

Job summary

PCI Pharma Services, a leading biopharma manufacturing services provider in California, seeks an Automation Engineer III to design, implement, and upgrade automated control systems for aseptic filling and related facilities. You will lead technical assessments, document GMP protocols, and collaborate across functions to ensure compliant, reliable operations.

The role requires a Bachelor's in a relevant field, 5–8 years of experience with at least 4 years in cGMP, and hands-on work with multiple

Qualifications

• Bachelor's degree in ChE, EE, IE, ME, CS or equivalent.
• 5–8 years of relevant engineering experience including 4+ years cGMP.
• Strong knowledge of automation standards including GAMP.
• Experience with multiple control platforms (vendor variety).

Responsibilities

• Design and specify automated control systems.
• Maintain and troubleshoot automation systems.
• Install automation hardware and software.
• Program control systems to meet requirements.
• Lead project upgrades and commissioning activities.
• Prepare GMP documentation (URS, FRS, IQ/OQ/PQ, SOP).
• Travel between facilities to support functions.

Skills

GAMP knowledge

GMP compliance

Cross-functional collaboration

Attention to detail

Education

Bachelor's degree in ChE/EE/IE/ME/CS or related

Tools

Allen Bradley

Siemens

Wonderware

iFix

Ignition

PI

Job description

PCI Pharma Services, a leading biopharma manufacturing services provider in California, seeks an Automation Engineer III to design, implement, and upgrade automated control systems for aseptic filling and related facilities. You will lead technical assessments, document GMP protocols, and collaborate across functions to ensure compliant, reliable operations.

The role requires a Bachelor's in a relevant field, 5–8 years of experience with at least 4 years in cGMP, and hands-on work with multiple