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Full Time Mastercontrol Jobs (NOW HIRING)

Inteldot

Document Coordinator

Barceloneta, PR · On-site

Employment type: Full time and onsite role Position Overview We are seeking an experienced ... Experience with document management systems such as Veeva, TrackWise, MasterControl, or similar ...

Medisca

QC Inspector

Irving, TX · On-site

Syspro/MasterControl an asset. * Ability to lift to 60 lbs. What's in it for you... We invest time ... We like to have fun - company events throughout the year * Full time positions - 40 hour work week

Pacelabs

GMP Document Management

Lebanon, NJ · On-site

$22/hr

Senior QA Associate- Full Time- Day Shift Administrative Position Compensation: $22.00 per hour ... Familiarity with electronic document management systems (e.g., MasterControl eDMS) * Experience ...

Pace

GMP Document Management

Lebanon, NJ · On-site

$22/hr

Senior QA Associate- Full Time- Day Shift Administrative Position Compensation: $22.00 per hour ... Familiarity with electronic document management systems (e.g., MasterControl eDMS) * Experience ...

PCI Pharma Services

Training Specialist

San Diego, CA · On-site

$26.73 - $30.07/hr

Prior experience with MasterControl or other eLMS systems preferred. * Ability to lead cross ... PCI offers full-time employees a competitive benefits package that includes paid time off, health ...

Align Technology

Global QMS Engineer

Raleigh, NC · On-site

$70K - $90K/yr

Quality Employment Type: Full Time Location: US-North Carolina-Raleigh Description This position is ... Experience working with electronic QMS tools (e.g., Arena PLM, Agile, Veeva, MasterControl, or ...

PCI Pharma Services

Training Specialist

San Diego, CA · On-site

$26.73 - $30.07/hr

Prior experience with MasterControl or other eLMS systems preferred. * Ability to lead cross ... PCI offers full-time employees a competitive benefits package that includes paid time off, health ...

Medisca

Quality Supervisor

Irving, TX · On-site

Experience with MasterControl is a strong asset What's in it for you... We invest time and ... We like to have fun - company events throughout the year * Full time positions - 40 hour work week

Medisca

Quality Supervisor

Plattsburgh, NY · On-site

$80K/yr

Experience with MasterControl is a strong asset What's in it for you... We invest time and ... We like to have fun - company events throughout the year * Full time positions - 40 hour work week

Verathon, Inc.

$115K - $231K/yr

Integrate AI tools with Verathon systems (e.g., Salesforce, Epicor, MasterControl, HRIS) following ... Employment Type: FULL_TIME

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Full Time Mastercontrol information

What is the difference between Full Time Mastercontrol vs Quality Assurance Specialist?

AspectFull Time MastercontrolQuality Assurance Specialist
CertificationsRelevant certifications like MasterControl certifications or quality management system trainingISO 9001, Six Sigma, or QA-specific certifications
Work EnvironmentRegulatory compliance, document control, software management in regulated industriesProduct testing, process audits, compliance checks in manufacturing or healthcare
Industry UsagePharmaceuticals, biotech, medical devices, regulated industriesManufacturing, healthcare, software development

Full Time Mastercontrol roles focus on managing quality management systems and document control using MasterControl software, often in regulated industries. Quality Assurance Specialists perform testing, audits, and compliance checks to ensure product quality. While both roles require quality-related knowledge, Mastercontrol professionals typically handle system administration, whereas QA Specialists focus on product and process quality assurance.

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Full Time Mastercontrol jobs near you

Document Coordinator

Inteldot

Barceloneta, PR • On-site

Full-time

Posted 17 days ago

Job description

Inteldot has over 15 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Employment type: Full time and onsite role
Position Overview
We are seeking an experienced Documentation Coordinator to support documentation management and coordination activities within a Biotech Drug Substance Manufacturing Operation in Barceloneta, Puerto Rico. The selected candidate will be responsible for coordinating the lifecycle of controlled GMP documentation, supporting document review and approval workflows, maintaining document control systems, and ensuring compliance with regulatory and internal quality standards. This role requires strong organizational skills, attention to detail, and the ability to work closely with cross-functional teams including Manufacturing, Quality, Engineering, Validation, and Operations in a fast-paced regulated manufacturing environment.
Key Responsibilities
  • Coordinate the routing, review, approval, issuance, revision, and archival of controlled GMP documentation
  • Manage document lifecycle activities for SOPs, batch records, forms, protocols, reports, and related manufacturing documentation
  • Ensure documentation complies with GMP requirements, FDA regulations, and internal quality standards
  • Support formatting, proofreading, consistency reviews, and document standardization efforts
  • Track document status, due dates, periodic reviews, and approval timelines
  • Collaborate with Subject Matter Experts (SMEs), Technical Writers, Manufacturing personnel, Quality Assurance, and Engineering teams to support documentation updates and implementation activities
  • Maintain accurate records within document management systems and ensure version control compliance
  • Assist with documentation metrics, reporting, and audit readiness activities
  • Support document change control processes and ensure proper documentation traceability
  • Participate in onsite meetings and coordination activities related to manufacturing documentation initiatives
Required Qualifications
  • Associate's or Bachelor's degree in Science, Business Administration, Engineering, or related field preferred
  • Minimum of 2 years of experience supporting document control or documentation coordination activities within biotech, pharmaceutical, medical device, or regulated manufacturing environments
  • Experience handling controlled GMP documentation and document management processes
  • Familiarity with GMP regulations, FDA documentation practices, and quality systems
  • Strong organizational, administrative, and coordination skills
  • Excellent written and verbal communication skills
  • Strong attention to detail and ability to manage multiple priorities simultaneously
  • Proficiency in Microsoft Office applications and electronic document management systems
  • Ability to work independently and collaboratively in a fast-paced manufacturing environment
  • Bilingual (English/Spanish)
Preferred Experience
  • Experience supporting Drug Substance or biologics manufacturing operations
  • Experience with document management systems such as Veeva, TrackWise, MasterControl, or similar platforms
  • Experience supporting audit readiness, remediation, or continuous improvement initiatives
Work Environment
  • Fully onsite position in Barceloneta, Puerto Rico
  • Manufacturing and operational support environment

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