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Internship Process Documentation Jobs in California

Manufacturing Intern

South San Francisco, CA · On-site

$20.50 - $26.75/hr

... process documentation, and production-line setup and improvements. * Support quality and testing ... Previous internship or project-based student org experience (Formula SAE, Rocketry, Design Build ...

Manufacturing Intern

South San Francisco, CA · On-site

$20.50 - $26.75/hr

... process documentation, and production-line setup and improvements. * Support quality and testing ... Previous internship or project-based student org experience (Formula SAE, Rocketry, Design Build ...

Interns will spend time working with community members, documenting, and conducting research to ... process as well as the intersection of public policy and grassroots advocacy.Outreach:

... testing, and manufacturing process documentation. First year: Own specific build and test ... Internship in at least one of: photovoltaics, power systems, or materials characterization * Hands ...

Internship Program Manager

Hawthorne, CA

$15.25 - $20.25/hr

... processes, university engagement, program coordination, and compliance with company policies and ... Maintain internship documentation and ensure OFCCP compliance with company policies and applicable ...

Internship Program Manager

Hawthorne, CA · On-site

$110K - $125K/yr

... processes, university engagement, program coordination, and compliance with company policies and ... Maintain internship documentation and ensure OFCCP compliance with company policies and applicable ...

Process Engineer

San Leandro, CA · On-site

$72K - $85K/yr

SOP documentation: Create and update standard operating procedures and work instructions. * Quality ... Internship or project experience in battery manufacturing * Experience with DOE, SPC, or Six Sigma ...

SOP documentation: Create and update standard operating procedures and work instructions. * Quality ... Internship or project experience in battery manufacturing * Experience with DOE, SPC, or Six Sigma ...

... processes, university engagement, program coordination, and compliance with company policies and ... Maintain internship documentation and ensure OFCCP compliance with company policies and applicable ...

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Internship Process Documentation information

What is the difference between Internship Process Documentation vs Internship Process Documentation?

AspectInternship Process Documentation
PurposeTo record and outline the steps involved in managing internships, including onboarding, training, and evaluation processes.
FocusProcess clarity, consistency, and compliance in internship programs.
Work EnvironmentAdministrative, HR, and program management settings.
Required SkillsProcess documentation, organizational skills, knowledge of internship programs.

Internship Process Documentation involves creating detailed records of internship procedures. It differs from roles like Internship Program Coordinator, which actively manages and implements internship programs. While documentation focuses on recording processes, coordinators execute and oversee the internship experience.

What are the most commonly searched types of Process Documentation jobs in California?

The most popular types of Process Documentation jobs in California are:

What cities in California are hiring for Internship Process Documentation jobs?

Cities in California with the most Internship Process Documentation job openings:

Operations Internship - Labeling Process & Formulation Laboratory

Cordis

Irvine, CA • On-site

$24/hr

Full-time

Posted 19 days ago


Job description

Overview
Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.
Responsibilities
The Operations Intern will support daily activities within the Labeling Process and Formulation Laboratory to ensure manufacturing operations comply with quality standards, regulatory requirements, and production schedules. This 6-month internship provides hands-on exposure to medical device manufacturing, documentation practices, quality systems, and laboratory operations in a regulated environment.
Key Responsibilities
Labeling Process
  • Assist with the preparation, verification, and issuance of product labels in accordance with approved procedures and regulatory requirements.
  • Support label reconciliation, inspection, and documentation activities.
  • Verify label accuracy, including product information, lot numbers, expiration dates, and barcode readability.
  • Participate in label change control and document revision processes.
  • Help maintain compliance with Good Documentation Practices (GDP) and Standard Operating Procedures (SOPs).

Formulation Laboratory
  • Assist laboratory personnel in preparing formulations, solutions, and materials according to established procedures.
  • Support laboratory testing, sample preparation, and data collection activities.
  • Maintain laboratory equipment cleanliness, calibration records, and inventory of chemicals and consumables.
  • Record experimental observations and maintain accurate laboratory documentation.
  • Follow laboratory safety protocols and Good Laboratory Practices (GLP).

Operations Support
  • Support production documentation, and quality records.
  • Collaborate with Manufacturing, Quality Assurance, Regulatory Affairs, and Engineering teams.
  • Perform other operational and administrative duties as assigned.

Qualifications
Required Qualifications
  • Currently pursuing a bachelor's degree in a related scientific discipline.
  • Strong interest in medical device manufacturing and regulated industries.
  • Basic understanding of laboratory practices and manufacturing operations.
  • Familiarity with Microsoft Office Suite (Excel, Word, PowerPoint).
  • Excellent organizational, analytical, and communication skills.
  • Ability to work independently and collaboratively in a team environment.
  • High attention to detail and commitment to quality and compliance.

Preferred Qualifications
  • Knowledge of ISO 13485, FDA Quality System Regulation (21 CFR Part 820), or Good Manufacturing Practices (GMP).
  • Experience with laboratory techniques or manufacturing environments through coursework or previous internships.
  • Exposure to Lean Manufacturing or Six Sigma concepts is an advantage.

Learning Outcomes
By the end of the internship, the intern will gain experience in:
  • Medical device manufacturing operations
  • Labeling compliance and documentation control
  • Formulation laboratory procedures
  • Quality Management Systems (QMS)
  • Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
  • Cross-functional collaboration within a regulated medical device environment
  • Continuous improvement and operational excellence principles

This description reflects responsibilities commonly assigned to operations interns in FDA- and ISO-regulated medical device manufacturing environments while providing meaningful exposure to both production labeling and laboratory processes
Pay / Compensation - The expected pre-tax pay rate for this position is $24 hourly
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.
Preferred Qualifications
Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one's identity. All our teammates' points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.