
CMC Regulatory Dossier Management (2 positions)
Alameda, CAContract / TemporarySeen 1 day agoSeen in employer's feed 1 day ago
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At a glance
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Job overview
System One is hiring a CMC Regulatory Dossier Management consultant for a one-year renewable contract supporting a pharmaceutical client. The role manages CMC-related regulatory submissions and documentation, including authoring, review, quality checks, archiving, and coordination with external partners. Candidates need regulatory information management experience and CMC knowledge. The position is fully onsite in Alameda, California.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Job Title: CMC Regulatory Dossier Management (2 positions)
Location: Alameda, California
Type: Contract (1-year, renewable)
Work Model: On-Site (100%)
Hours: 8am-5pm, m-f, fully onsite
Overview
Our pharma client is hiring a CMC Regulatory Dossier Management consultant for a 1 year renewable contract. This opportunity requires a candidate with strong Regulatory Information Management systems (RIM) experience.
Responsibilities
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Support the development of high quality, phase appropriate CMC-related submissions to health authorities by managing the authoring, review, and approval of regulatory documentation.
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Manage the document review process and schedule meetings to ensure documentation timelines are achieved, providing status updates as necessary to stakeholders.
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Manage the QC check of regulatory documentation by technical SMEs and ensure appropriate archiving of source technical documents.
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Facilitate domestic and global regulatory lifecycle submissions through the management of supporting technical and regulatory documentation requests with external partners and vendors.
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Ensure continued regulatory compliance and phase appropriate, risk-based approaches to manufacturing flexibility while adhering to change control procedures and health authority requirements.
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Contribute to the development and maintenance of the working practices and procedures, as well as help update and maintain procedures, templates and documents.
Requirements
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BA/BS and 2-4 years of experience in medical/technical writing; or MS and 1 years of experience in technical (CMC) or regulatory writing.
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Minimum 5 years experience in the pharmaceutical or biotech industries.
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Possess Chemistry, Manufacturing and Controls (CMC) knowledge experience through the support of manufacturing operations in a technical or quality role.
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Familiarity with Common Technical Document content templates, as well as content expectations for IND/NDA/BLA/MAA or other regulatory documentation.
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Experience with electronic regulatory information management systems, such as Veeva, recommended.
System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#LI-
Ref: #568-Clinical
System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
How this job compares
Set against the 993 open Regulatory Affairs jobs on Olive Jobs, counted November 14, 2026.
- Pay
- This postingNot listed
- California median$146–203K/yr118 salary ranges
- US median$28–40/hr46 hourly ranges
- Openings
- Olive Jobs lists 158 open Regulatory Affairs jobs in California and 993 across the US. 17% of them nationwide are listed as remote or flexible.
- Hiring the most in California
- Gilead Sciences, Inc.21 open
- BeOne Medicines17 open
- Abbott10 open
- Experience
- This posting asks for at least 5 years of experience; Regulatory Affairs postings that state a minimum ask for 7 years at the median (883 postings).
- Education
- 596 of the 993 open Regulatory Affairs jobs (60%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 14, 2026. Figures based on too few postings are left out.
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