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Mastercontrol Jobs in California (NOW HIRING)

Penumbra

DHR Reviewer I - Temp

Alameda, CA · On-site

$22 - $32/hr

Proficiency with MasterControl preferred. * Strong oral, written, and interpersonal communication skills. Working Conditions General office environment. Willingness and ability to work on site.

Pivotal Systems

Quality Manager

Fremont, CA · On-site

Experience implementing or administering document control systems, ideally within an eQMS platform (e.g., MasterControl, Arena, Qualio, ETQ, or similar). * Experience developing or unifying QMS ...

Pivotal Systems

Quality Manager

Fremont, CA

Experience implementing or administering document control systems, ideally within an eQMS platform (e.g., MasterControl, Arena, Qualio, ETQ, or similar). * Experience developing or unifying QMS ...

Orca Bio

Senior Specialist, Global QMS

Sacramento, CA · On-site +1

$90K - $120K/yr

MasterControl, ERP systems, Trackwise, etc.) ensuring alignment with regulatory and internal requirements. * Collaborate with cross-functional and site leadership teams to drive continuous ...

New

Orca Bio

Senior Specialist, Global QMS

Sacramento, CA · On-site +1

$90K - $120K/yr

MasterControl, ERP systems, Trackwise, etc.) ensuring alignment with regulatory and internal requirements. * Collaborate with cross-functional and site leadership teams to drive continuous ...

New

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Mastercontrol information

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$29

$49

$86

How much do mastercontrol jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for mastercontrol in California is $49.41, according to ZipRecruiter salary data. Most workers in this role earn between $36.72 and $63.79 per hour, depending on experience, location, and employer.

What is a Mastercontrol?

A MasterControl job typically involves managing and administering the MasterControl quality management software, which is used in regulated industries like pharmaceuticals, medical devices, and manufacturing. Professionals in this role ensure compliance with industry standards, maintain document control, and streamline quality processes. Responsibilities may include system configuration, user training, troubleshooting, and supporting audits. Strong knowledge of quality regulations (e.g., FDA, ISO) and experience with electronic document management systems are often required.

What are the key skills and qualifications needed to thrive in the Mastercontrol position?

To thrive as a Master Control Operator, you need a solid understanding of broadcast operations, signal monitoring, and troubleshooting, often supported by relevant experience or technical training in broadcasting or electronics. Familiarity with broadcast automation systems, video servers, and FCC regulations is essential, with some employers preferring industry certifications. Attention to detail, quick decision-making, and strong communication skills help ensure smooth operations, especially under tight deadlines. These skills are crucial for maintaining broadcast quality, meeting regulatory standards, and minimizing on-air disruptions.

What are the most common challenges faced by Master Control Operators in day-to-day operations?

Master Control Operators often encounter fast-paced situations where they must quickly resolve technical issues such as signal interruptions, audio/video mismatches, or last-minute schedule changes. Maintaining flawless broadcast quality under strict time constraints can be challenging, especially when coordinating with production teams and adhering to regulatory guidelines. Effective multitasking and attention to detail are essential for minimizing errors and preventing on-air disruptions. Those who excel in this role are adept at troubleshooting and remain calm under pressure, ensuring reliable and seamless broadcasts.

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

The most popular types of Mastercontrol jobs in California are:

What are popular job titles related to Mastercontrol jobs in California?

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

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

The top searched job categories for Mastercontrol jobs in California are:

What cities in California are hiring for Mastercontrol jobs?

Cities in California with the most Mastercontrol job openings:

Mastercontrol jobs near you
Infographic showing various Mastercontrol job openings in California as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution, with an average salary of $102,782 per year, or $49.4 per hour.

Quality Systems Associate (Contract)

ORIC Pharmaceuticals

San Diego, CA • On-site

$25 - $33.50/hr

Contractor

Posted 2 days ago

New

Job description

Company Description
ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn.
Reporting to the Quality Systems Specialist, the Quality Systems Associate will support document control, training, and quality systems activities, providing word processing, archival and electronic system maintenance. The successful candidate will work closely with Quality Assurance, Technical Operations, Clinical, Regulatory and third-party Contract organizations.
Job Description
  • Support document processing, review and release of regulated GxP documents .
  • Collaborate closely with document owners to resolve any documentation discrepancies identified during review.
  • Organize review and support activities to ensure timely review and completion of documentation task to meet pre-established timelines.
  • Participate in cross functional program meetings to provide appropriate QA updates.
  • Maintain and update electronic quality systems, documentation files and folders in accordance with written SOPs.
  • Facilitate/coordinate GMP training for internal employees/departments as required.
  • Identify and facilitate continuous improvement of internal Policies, SOPs and Work Instructions, as needed.
  • Provide document support for internal audits and regulatory inspections, as needed.
  • Perform all duties in keeping with ORIC's core values, policies and all applicable regulations.

Qualifications
  • Bachelor's degree or equivalent relevant experience.
  • 0-2 years of relevant experience in Quality Assurance or experience in an academic or regulated environment.
  • Highly polished writing and editing skills.
  • High degree of proficiency in Microsoft Office Suite.
  • Knowledge of GMP regulations and guidance documents is preferred, including but not limited to:
    • 21 CFR Parts 11, 210, 211
    • Applicable ICH Quality Guidelines for Good Manufacturing Practices (GMP)
    • EU EudraLex Volume 4
  • Experience with electronic quality management systems such as Veeva or MasterControl is a plus.
  • Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment that includes external partners. Proven ability to manage multiple priorities and deliver high-quality work.
  • Demonstrated initiative, ownership, problem identification, problem solving, and strategic thinking skills.
  • Demonstrated ability to quickly adapt and find creative solutions to ensure deliverables are met.
  • Excellent verbal and written communication skills

Additional Information
The anticipated hourly rate for candidates who will work on-site at our San Diego location is between $25.00-$33.50 per hour. The final rate offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. This position is not eligible for H-1B visa sponsorship.
ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.

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