820 Process Engineer Manufacturing jobs in Berkeley,CA

Bachelor's degree in Engineering (Mechanical, Electrical, Chemical, or related discipline)
Minimum 10-12 years of progressive engineering management experience, with 5+ years in pharmaceutical or biotechnology environments.
Demonstrated experience managing complex facility engineering operations.
Strong background in asset lifecycle management
CMMS systems (SAP preferred)
CAD/CAFM platforms
Predictive maintenance technologies.
Experience with pharmaceutical facility systems including HVAC, utilities, process equipment, and regulatory compliance requirements (FDA, EMA).
Proven ability to lead cross-functional teams, manage multiple concurrent projects, and drive organizational change.
Strong analytical and problem-solving capabilities with experience developing strategic initiatives that improve operational performance.
Excellent written and verbal communication skills with ability to present complex technical information to diverse audiences.
Experience working in matrix organizations and managing vendor relationships.

Bay Area Rapid Transit (BART)

Hayward, CA 94544

Velo3D

Fremont, CA 94538

High school diploma or equivalent, with 5+ years of experience in quality inspection or quality assurance within a manufacturing environment.
Ability to read and interpret mechanical and electrical engineering drawings
Proficiency with standard hand measurement tools: calipers, micrometers, gauges, and related equipment
Experience inspecting both mechanical and electromechanical components and assemblies
Strong attention to detail with the ability to document findings clearly and completely
Comfortable working in a production floor environment

Huntington San Francisco

San Francisco, CA 94108

The United States Secret Service

Oakland, CA 94604

Adecco

Cupertino, CA 95014

Bachelor's degree or equivalent relevant experience
2–5 years of experience in medical device labeling or regulatory labeling support
Strong understanding of global medical device labeling regulations, including 21 CFR 801 and EU MDR
Knowledge of Quality Management Systems (QMS), including design control, document control, and regulatory approval processes
Excellent written and verbal communication skills
Strong interpersonal skills with experience working across multiple cross-functional teams
Highly organized with strong attention to detail and time management skills
Ability to work independently and manage multiple priorities
Technical writing experience preferred