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Mastercontrol Jobs in California (NOW HIRING)

Experience with electronic Quality Management Systems ( eQMS ) and platforms such as Veeva, TrackWise, MasterControl or similar. * Understanding of cGMP requirements, Change Control processes and ...

New

QA Specialist II

Vista, CA · On-site

$35 - $52/hr

Support system and process harmonization initiatives across sites and electronic quality systems (e.g., MasterControl). Qualifications * Bachelor's degree in a science-related field required; Master ...

MasterControl). * Works on problems of diverse scope; exercises good judgement in selecting methods and techniques for obtaining solutions while handling Quality Assurance tasks. * Proficient in ...

Experience with electronic QMS platforms (MasterControl, Greenlight Guru, or equivalent) Preferred Qualifications * Experience with combination product quality requirements * Background in design ...

Document Control Manager

Oxnard, CA · On-site

$75 - $95/hr

Experience with an eQMS or document management platform such as MasterControl, Veeva, Greenlight Guru, or an equivalent, a plus. Conversational Spanish a plus. Valid California driver's license and ...

Posted today

Document Control Manager

Oxnard, CA · On-site

$75K - $95K/yr

... such as MasterControl, Veeva, Greenlight Guru, or an equivalent, a plus. • Conversational Spanish a plus. • Valid California driver's license and the ability to travel regularly between our ...

New

Experience with Salesforce and MasterControl or similar CRM and document control system. * Hands-on experience with instrumentation and laboratory equipment; experience as an end-user of related ...

FSQA Technician

San Bernardino, CA · On-site

$20 - $23/hr

SafetyChain / Redzone / TraceGains / MasterControl or other FSQA and productivity software user experience. Certifications: * HACCP certification, SQF or BRC knowledge. Key Competencies & Traits:

DHR Reviewer I - Temp

Alameda, CA · On-site

$22 - $32/hr

... MasterControl preferred. • Strong oral, written, and interpersonal communication skills. Working Conditions General office environment. Willingness and ability to work on site. Requires some ...

Drafter

Rancho Cordova, CA · On-site

$44K - $59K/yr

Become proficient in software tools such as SolidWorks, Inventor, PDM, Vault, Altium, PADs, and MasterControl * Facilitate Engineering Change Proposals (ECPs) and incorporate Engineering Change ...

Drafter

Rancho Cordova, CA · On-site

$44K - $59K/yr

Become proficient in software tools such as SolidWorks, Inventor, PDM, Vault, Altium, PADs, and MasterControl * Facilitate Engineering Change Proposals (ECPs) and incorporate Engineering Change ...

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

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.

Showing results 21-40

Mastercontrol information

See California salary details

$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 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:

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.

Project Administrator

SoTalent

Vacaville, CA • On-site

Other

Posted yesterday

New


Job description

Project Administrator – Technology Transfer & CAPEX

Location: Vacaville, CA

Industry: Biotechnology / Pharmaceuticals / Life Sciences / Biomanufacturing

About the Role

A global life sciences organisation is seeking a Project Administrator to support Technology Transfer and CAPEX projects within a highly regulated biopharmaceutical manufacturing environment.

The role focuses on Change Control management, project coordination, documentation, compliance and cross-functional delivery, working closely with Project Managers, Quality, Manufacturing, Engineering, Validation, Regulatory and Supply Chain teams.

Key Responsibilities

  • Manage Change Controls throughout the full project lifecycle, from initiation through final closure.
  • Coordinate action items, approvals and implementation activities to ensure projects remain on schedule.
  • Monitor project timelines, identify risks and bottlenecks, and escalate issues proactively.
  • Coordinate with cross-functional teams to support effective and compliant change implementation.
  • Schedule and facilitate project meetings, prepare minutes and track actions through completion.
  • Support project planning, status tracking, risk management and stakeholder coordination.
  • Maintain accurate, complete and audit-ready project documentation.
  • Prepare project status reports, milestone updates and stakeholder communications.
  • Ensure project records and Change Controls comply with applicable SOPs and cGMP requirements.
  • Support inspection readiness and regulatory compliance activities.
  • Drive accountability across stakeholders to ensure project milestones and business objectives are achieved.

Qualifications

  • Bachelor's degree in Life Sciences, Biotechnology, Engineering, Quality, Business Administration or a related field, or equivalent practical experience.
  • 2+ years of experience in biotechnology, pharmaceutical, medical device or another cGMP-regulated manufacturing environment.
  • Direct experience coordinating or managing Change Controls and Quality Systems.
  • Experience with electronic Quality Management Systems (eQMS) and platforms such as Veeva, TrackWise, MasterControl or similar.
  • Understanding of cGMP requirements, Change Control processes and regulated manufacturing environments.
  • Strong project coordination, organisational and stakeholder management skills.
  • Excellent written and verbal communication abilities.
  • Ability to manage multiple projects and priorities while maintaining accuracy and compliance.
  • Exceptional attention to detail and strong documentation discipline.

Preferred Background

  • Quality Assurance / Quality Systems / Compliance
  • Pharmaceutical or Biotech Manufacturing
  • Engineering or Validation
  • Technology Transfer
  • Project Administration / Project Coordination

Industry

Biotechnology | Pharmaceuticals | Life Sciences | Biomanufacturing | Quality & Compliance | Technology Transfer | Project Management