Kelly Science, Engineering, Technology & Telecom
Document Control Specialist
Kelly Science, Engineering, Technology & Telecom, South San Francisco, California, us, 94083
Kelly Science, Engineering, Technology & Telecom provided pay range
This range is provided by Kelly Science, Engineering, Technology & Telecom. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $35.00/hr - $40.00/hr
Recruiter at Kelly Science, Engineering, Technology & Telecom Kelly® Science & Clinical is seeking a Document Control Specialist for a 12‑month contract position at a leading biotech company client in South San Francisco, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay Rate:
$35‑40/hour
Overview In this role, you will ensure the integrity, accuracy, and compliance of GMP documentation and training records within the Quality Management System (QMS), directly contributing to the advancement of innovative cancer therapies in a dynamic, highly regulated environment.
Schedule Part time (up to 20 hours/week), hybrid schedule
Responsibilities
Manage, track, review, and maintain GMP‑related documents within the QMS, primarily using MasterControl.
Ensure documentation meets compliance and company standards.
Administer training records and support training logistics, ensuring documentation is up‑to‑date and accurately reflected in the system.
Support minor change control activities, facilitating document updates and revisions in accordance with company procedures.
Take initiative in resolving minor issues related to document management and training.
Recommend and implement methods to increase efficiency and effectiveness within your scope.
Ensure all actions comply with relevant pharmaceutical industry regulations and internal policies.
Work closely with cross‑functional teams (Quality, Regulatory, etc.), demonstrating professionalism and adaptability in a remote environment.
Qualifications
4+ years of experience in document control or quality systems within pharmaceutical, biotech, or related regulated industries.
Hands‑on experience with QMS, specifically MasterControl or comparable software.
Experience with GMP documentation practices.
Comfortable working independently and troubleshooting minor challenges.
Seniority level
Associate
Employment type
Part‑time
Job function
Quality Assurance
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Base pay range $35.00/hr - $40.00/hr
Recruiter at Kelly Science, Engineering, Technology & Telecom Kelly® Science & Clinical is seeking a Document Control Specialist for a 12‑month contract position at a leading biotech company client in South San Francisco, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay Rate:
$35‑40/hour
Overview In this role, you will ensure the integrity, accuracy, and compliance of GMP documentation and training records within the Quality Management System (QMS), directly contributing to the advancement of innovative cancer therapies in a dynamic, highly regulated environment.
Schedule Part time (up to 20 hours/week), hybrid schedule
Responsibilities
Manage, track, review, and maintain GMP‑related documents within the QMS, primarily using MasterControl.
Ensure documentation meets compliance and company standards.
Administer training records and support training logistics, ensuring documentation is up‑to‑date and accurately reflected in the system.
Support minor change control activities, facilitating document updates and revisions in accordance with company procedures.
Take initiative in resolving minor issues related to document management and training.
Recommend and implement methods to increase efficiency and effectiveness within your scope.
Ensure all actions comply with relevant pharmaceutical industry regulations and internal policies.
Work closely with cross‑functional teams (Quality, Regulatory, etc.), demonstrating professionalism and adaptability in a remote environment.
Qualifications
4+ years of experience in document control or quality systems within pharmaceutical, biotech, or related regulated industries.
Hands‑on experience with QMS, specifically MasterControl or comparable software.
Experience with GMP documentation practices.
Comfortable working independently and troubleshooting minor challenges.
Seniority level
Associate
Employment type
Part‑time
Job function
Quality Assurance
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