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Medical Script Jobs in California (NOW HIRING)

Modular Medical Inc

Customer Care Manager

San Diego, CA · On-site

Modular Medical built Pivot™ for those people: the "almost-pumpers." Pivot is a tubeless insulin ... Develop call scripts that address customer inquiries clearly and consistently. * Assess staffing ...

Kitu Systems

Software Test Engineer

San Diego, CA

... test cases, scripts, and tools to implement test plans Develop scripts and tools to automate ... that includes Medical, Dental, Vision, and Life Coverage in addition to PTO. The position is ...

Kitu Systems

Software Test Engineer

San Diego, CA · On-site

... scripts, and tools to implement test plans • Develop scripts and tools to automate testing • ... that includes Medical, Dental, Vision, and Life Coverage in addition to PTO. The position is ...

Katalyst CRO

CSV Engineer

Redwood City, CA · On-site

... scripts • Managing change controls including creation, execution, and closure • Supporting data ... and medical device companies worldwide. Founded in , the company is headquartered in South ...

Rivian

Sr. Battery Cell Test Engineer

Tustin, CA · On-site

Write test scripts and set up programs to run tests automatically with different cyclers and ... medical, dental, vision, short-term disability insurance, and long-term disability insurance to ...

Rivian

Sr. Battery Cell Test Engineer

Tustin, CA · On-site

Write test scripts and set up programs to run tests automatically with different cyclers and ... medical, dental, vision, short-term disability insurance, and long-term disability insurance to ...

Rivian

Sr. Battery Cell Test Engineer

Tustin, CA · On-site

Write test scripts and set up programs to run tests automatically with different cyclers and ... medical, dental, vision, short-term disability insurance, and long-term disability insurance to ...

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Medical Script information

See California salary details

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$28

How much do medical script jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for medical script in California is $20.27, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $22.55 per hour, depending on experience, location, and employer.

What is a medical script?

A Medical Script job typically involves writing or reviewing medical documents, such as prescriptions, treatment plans, or healthcare-related scripts for media and patient education. Professionals in this role require knowledge of medical terminology and compliance with healthcare regulations. They may work in hospitals, clinics, pharmaceutical companies, or media agencies to ensure accuracy and clarity in medical communication.

What does a typical workday look like for a medical script?

A typical workday as a Medical Scribe involves accompanying physicians during patient visits, either in-person or remotely, and documenting clinical encounters in real time using electronic health record (EHR) systems. You will capture detailed notes on patient history, physical exams, and treatment plans, ensuring that all documentation is accurate and complete before the physician finalizes it. Scribes also help manage clinical workflows by tracking lab results, orders, and patient follow-ups. You'll work closely with medical teams in a fast-paced environment, gaining valuable firsthand experience in healthcare settings that can be beneficial for future career growth.

What are the key skills and qualifications needed to thrive in the medical script position, and why are they important?

As a Medical Scribe, you need a strong understanding of medical terminology, attention to detail, and fast, accurate typing skills, typically supported by relevant coursework or healthcare experience. Familiarity with electronic health record (EHR) systems and, in some cases, scribe certification is highly valued. Excellent listening, communication, and time management skills help you collaborate effectively with physicians and healthcare staff. These abilities are essential for creating precise documentation that supports high-quality patient care and smooth clinical operations.

What are popular job titles related to Medical Script jobs in California?

For Medical Script jobs in California, the most frequently searched job titles are:

What job categories do people searching Medical Script jobs in California look for?

The top searched job categories for Medical Script jobs in California are:

What cities in California are hiring for Medical Script jobs?

Cities in California with the most Medical Script job openings:

Medical Script jobs near you
Infographic showing various Medical Script job openings in California as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 18% Part Time, and 7% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $42,162 per year, or $20.3 per hour.

Software Medical Device Engineer

Stark Pharma Solutions Inc

Pleasanton, CA • On-site

Contractor

Re-posted 5 days ago

Job description

Location: Pleasanton, CA .  

The contract is for 1 year.  

RESPONSIBILITIES:
• Plan and execute migration of requirements and related data from legacy tools (e.g., DOORS, Jama, Excel, Jira) into new platforms, ensuring data integrity, traceability, and compliance.
• Administer, configure, and maintain enterprise requirements management tools, including hierarchies, templates, workflows, versioning, and baselining in alignment with the quality system.
• Develop and maintain a requirements management plan in collaboration with cross‑functional teams, defining the overall requirements structure and links to associated design control documents.
• Create and maintain standardized requirements templates, traceability frameworks, and governance models based on quality and regulatory requirements.
• Maintain the requirements database, develop scripts or automation as needed, and support integrations or add‑in tools to improve usability and efficiency.
• Provide training, documentation, and ongoing support to engineers, serving as the primary functional expert for requirements tools and best practices.
REQUIRED QUALIFICATIONS:
• Bachelor’s degree in Engineering, Computer Science, Biomedical Engineering, or a related discipline for requirements management.
• A minimum of 5 years with hands on experience administering or configuring enterprise requirements management tools to support regulated development environments (e.g., Codebeamer, DOORS, Jama, or comparable platforms). Ability to quickly learn and adopt new tools is expected.
• Hands‑on experience with requirements migration from legacy tools.
• Strong understanding of medical device product development and design control principles.
• Excellent verbal and written communication skills, with the ability to train and support engineers at all levels.
• Ability to work effectively in a collaborative environment.
PREFERRED QUALIFICATIONS:
• Experience acting as a tool administrator, configuration owner, or advanced power user in a regulated development environment.
• Experience defining or scaling requirements management frameworks for large or multi‑team programs.
• Familiarity with medical device development (FDA 21 CFR Part 820) with the ability to configure tools to support compliant workflows.
• Experience supporting software‑driven, connected, or mobile medical devices.
• Experience with different requirements management or lifecycle tools is valued; strong foundational understanding of requirements structures and traceability is more important than experience with a specific platform.
Abbott’s Heart Failure division is seeking a Requirements Tools Engineer to support medical device development by enabling and maintaining enterprise requirements management infrastructure. The role focuses on administering, configuring, and optimizing requirements tools, migrating data from legacy systems (e.g., DOORS, Jama, Excel, Jira), and ensuring data integrity, traceability, and regulatory compliance. The engineer collaborates with cross functional teams to define scalable requirements structures, templates, workflows, versioning, and baselining aligned with quality systems. Responsibilities also include developing requirements management plans, maintaining databases, supporting integrations or automation, and acting as the functional expert through training and ongoing support. The role requires 5+ years of hands on experience with enterprise requirements tools in regulated environments, strong knowledge of medical device design controls, and excellent communication skills. Experience with FDA 21 CFR Part 820, large scale programs, and software driven medical devices is preferred.