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Process Equipment Maintenance Specialist III

PCI Pharma Services · San Diego, CA

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Level
Senior
Team
Reliability
Experience asked
8+ years
Industry
Pharma & life sciences
Posted
2 days ago

The role in 30 seconds

A senior reliability role at PCI Pharma Services (pharma & life sciences) in San Diego, CA. Author, review, and update maintenance procedures and forms.

They ask for
8+ years
Tools it names
FDA / GMP, PLC

Read from the posting. The full description is below.

From the plant jobs report · week of November 2, 2026

Reliability Engineer roles in California: typical posted base $115k–$178k.

Median of the low and high ends of 73 live postings that list pay, out of 162 reliability engineer openings in California, read from manufacturers' own careers sites.

California plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 161 other live reliability postings in California.

Base pay
Not listed in this posting

Typical $115k–$178k, from 72 postings that list pay.

Experience asked
More than usual (8+ vs 5+)

Similar roles usually ask 5+ years.

Skills these teams ask for most

  • Root cause 67%
  • New product launch 44%
  • FMEA 35%
  • Automation 31%
  • Validation (IQ/OQ/PQ) 22%
  • SPC 22%

✓ = this posting asks for it too. % = share of similar postings that mention it.

Stands out: this posting asks for FDA / GMP, PLC, Union environment, which few similar roles mention. If you have it, lead with it.

It asks for 8+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Reliability team at PCI Pharma Services

    We found 4 people at this company and state: 3 in this kind of role, 1 leaders. Engineers who joined in the last year or two reply the most. See them ↓

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

    Write to Richard → (free)
  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: PCI Pharma Services in San Diego

4 other open roles at this site · 4 people we found in reliability roles at PCI Pharma Services.

Full description from PCI Pharma ServicesAs posted on their careers site.Show

Responsibilities

  • ◆Troubleshoot complex problems, complete emergency repairs, and guide staff in implementing repairs.
  • ◆Maintain equipment in use-ready, compliant state. Major equipment includes lyophilizer, PLC, SCADA, HMI, clean steam, WFI, Autoclaves, Depy Ovens and others.
  • ◆Monitor, respond to, and correct issues generating equipment alarms.
  • ◆Provide recommendation for, and implement upgrades and improvements.
  • ◆Author, review, and update maintenance procedures and forms.
  • ◆Complete CMMS entries and required training activities.
  • ◆Travel between facilities to support all functional areas.
  • ◆Regular and reliable attendance on a full time basis [or in accordance with posted schedule].
  • ◆Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.

Qualifications

  • ✓High school diploma or equivalent experience required.
  • ✓Minimum of 8 years of relevant experience required.
  • ✓Minimum of 4 years of cGMP experience required.
  • ✓Advanced mechanical and electrical troubleshooting skills.
  • ✓Ability to read and understand equipment schematics.
  • ✓General understanding of support equipment.
  • ✓Experience with components such as PLCs, VFDs, and servos.
  • ✓Experience with safety circuits.
  • ✓Experience with aseptic filling is preferred but not required.
  • ✓Ability to work in a group, and independently.
  • ✓Strong working knowledge of GMP, aseptic techniques, and laboratory compliance
  • ✓Highly proficient in Microsoft Office applications.
  • ✓Excellent attention to detail, critical thinking, and communication skills.
  • ✓Able to work autonomously, drive results, and collaborate in a cross-functional environment.

The hiring rate for this position is $40.92 - 46.04/hour plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), flexible spending account, and 401(k). ​

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Show full description ↓

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Schedule: 2nd Shift

Generally: 2:00pm - 10:30pm

Summary

This position is responsible for maintaining and improving and/or upgrading process support equipment for biopharmaceutical manufacturing and aseptic filling operations. The role supports operations in ensuring use-ready and compliant equipment, including advanced troubleshooting, preventive maintenance, upgrade, and authoring, review, update, and completion of CMMS and GMP-related documentation.

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