Mirador Therapeutics
Associate Director, CMC Technical Writing
Mirador Therapeutics - San Diego, California, United States, 92154
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Overview
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Associate Director, CMC Technical Writing - San Diego, CA
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Mirador Therapeutics 2 days ago Be among the first 25 applicants Join to apply for the
Associate Director, CMC Technical Writing - San Diego, CA
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Mirador Therapeutics Mirador is a next-generation precision medicine company focused on immunology and inflammation. The company’s Mirador360 TM precision development engine leverages the latest advances in human genetics and cutting-edge data science to rapidly advance new precision medicines for patients living with chronic immune-mediated inflammatory and fibrotic diseases. Launched in 2024, Mirador has raised over $400 million from leading life sciences investors and is based in San Diego, CA.
Not sure what skills you will need for this opportunity Simply read the full description below to get a complete picture of candidate requirements.
Summary
We are seeking a motivated individual to join our CMC team and be responsible for assembling, managing, and writing the quality sections of CMC submissions and associated technical documents for biological and small molecule assets. This individual will be embedded in technical teams within the CMC department supporting our growing pipeline projects and contribute to developing clinical and commercial programs.
Responsibilities
Manage the preparation and review of technical contributions to critical clinical and commercial programs, including INDs, IMPDs, BLAs, NDAs, MAAs, and associated questions from Regulatory Authorities, including post-approval changes. Assemble and/or author the necessary CMC reports from source documents such as process performance qualification protocol/ reports, method validation reports, specifications, COAs, stability protocols, stability data. Responsible for working with third party vendors on source documentation review and approval. Provide risk assessments for CMC changes, deviations, strategic mitigations plans, manufacturing site transfers, nitrosamines, PGIs, etc. while working with Regulatory so they can properly reflect the information in regulatory filings. Work cross-functionally with CMC, Regulatory, and QA colleagues to ensure consistency across regulatory and technical documents.
Experience And Qualifications
Bachelor’s degree in a scientific discipline required, advanced degree (Master’s or PhD degree) strongly preferred. 8 years or more of previous biotechnology/pharmaceutical industry is required. Experience with quality sections (Module 3) for global regulatory submissions. Proficient in high quality technical writing. Experience with Veeva, eCTD templates, and the Microsoft suite of programs.
Skills And Abilities
Leadership capabilities for cross functional teams with exceptional organizational and communication skills. Ability to work on several projects and assignments at the same time, with appropriate prioritization. A commitment to collaborative leadership, management, teamwork, delegation and fostering a professional culture based on trust and mutual respect in a fast-paced environment. Competent in reviewing, analyzing, and assembling source data to convey accuracy in the required regulatory filings. Ability to work well under pressure and meet time sensitive deadlines. Ability to work across locations and time zones. Highly proficient using Microsoft Word, Excel, PowerPoint, Project, SharePoint, Starting Point templates, or similar applications and systems.
The expected base pay range for this position is $170,000 - $210,000 plus bonus, equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. This range may be modified in the future.
All qualified applicants are considered for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, veteran status or other protected class.
Read our Job Applicant Privacy Policy
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Employment typeFull-time Job function
Job functionInformation Technology Referrals increase your chances of interviewing at Mirador Therapeutics by 2x Sign in to set job alerts for “Associate Technical Director” roles. San Diego, CA $170,000.00-$210,000.00 10 hours ago Senior Project Manager, Customer ExperienceSupply Chain Manufacturing Operational Excellence TPM/IWS - Manager - Consulting - Location OPENSr. Software Engineer - Payments Support San Diego, CA $80,000.00-$110,000.00 6 hours ago Sr. Software Engineer - Investment ManagerSenior Software Engineer – SOC Power/Thermal software - AutomotiveHydraulic Modeling & Analysis - Senior Project Manager - Water, Wastewater & Recycled Water (Option for Remote)Senior Software Engineer – Localization and State Estimation (R3123)Senior Project Manager- Water Conveyance/Pump StationsSenior Program Project Manager (Exp in Regulatory or Medical Device Industry)Senior Project Manager - Transmission Routing and SitingSr. Project/Program Manager (Min 5 Yrs. Healthcare Exp.)Associate Technical Director - Bridge, for COWI in North AmericaSenior Principal Embedded Software Engineer -Onsite (Strong C++ & real-time/embedded systems area)Automotive - Platform Software Engineer (Staff-Sr. Staff Position)Senior or Software Technical Product Manager 2 (Engineering)Senior Systems Engineer – Software Focus (Remote / Flexible) San Diego, CA $126,536.00-$161,684.00 9 hours ago Sr. Superintendents, Project Managers, Sr. Projects EngineersSenior Project Manager - up to $190K (Educational Exp*) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Associate Director, CMC Technical Writing - San Diego, CA
role at
Mirador Therapeutics 2 days ago Be among the first 25 applicants Join to apply for the
Associate Director, CMC Technical Writing - San Diego, CA
role at
Mirador Therapeutics Mirador is a next-generation precision medicine company focused on immunology and inflammation. The company’s Mirador360 TM precision development engine leverages the latest advances in human genetics and cutting-edge data science to rapidly advance new precision medicines for patients living with chronic immune-mediated inflammatory and fibrotic diseases. Launched in 2024, Mirador has raised over $400 million from leading life sciences investors and is based in San Diego, CA.
Not sure what skills you will need for this opportunity Simply read the full description below to get a complete picture of candidate requirements.
Summary
We are seeking a motivated individual to join our CMC team and be responsible for assembling, managing, and writing the quality sections of CMC submissions and associated technical documents for biological and small molecule assets. This individual will be embedded in technical teams within the CMC department supporting our growing pipeline projects and contribute to developing clinical and commercial programs.
Responsibilities
Manage the preparation and review of technical contributions to critical clinical and commercial programs, including INDs, IMPDs, BLAs, NDAs, MAAs, and associated questions from Regulatory Authorities, including post-approval changes. Assemble and/or author the necessary CMC reports from source documents such as process performance qualification protocol/ reports, method validation reports, specifications, COAs, stability protocols, stability data. Responsible for working with third party vendors on source documentation review and approval. Provide risk assessments for CMC changes, deviations, strategic mitigations plans, manufacturing site transfers, nitrosamines, PGIs, etc. while working with Regulatory so they can properly reflect the information in regulatory filings. Work cross-functionally with CMC, Regulatory, and QA colleagues to ensure consistency across regulatory and technical documents.
Experience And Qualifications
Bachelor’s degree in a scientific discipline required, advanced degree (Master’s or PhD degree) strongly preferred. 8 years or more of previous biotechnology/pharmaceutical industry is required. Experience with quality sections (Module 3) for global regulatory submissions. Proficient in high quality technical writing. Experience with Veeva, eCTD templates, and the Microsoft suite of programs.
Skills And Abilities
Leadership capabilities for cross functional teams with exceptional organizational and communication skills. Ability to work on several projects and assignments at the same time, with appropriate prioritization. A commitment to collaborative leadership, management, teamwork, delegation and fostering a professional culture based on trust and mutual respect in a fast-paced environment. Competent in reviewing, analyzing, and assembling source data to convey accuracy in the required regulatory filings. Ability to work well under pressure and meet time sensitive deadlines. Ability to work across locations and time zones. Highly proficient using Microsoft Word, Excel, PowerPoint, Project, SharePoint, Starting Point templates, or similar applications and systems.
The expected base pay range for this position is $170,000 - $210,000 plus bonus, equity, and comprehensive benefits. The base pay range reflects the target range for this position, but individual pay will be determined by additional factors such as job-related skills, experience and relevant education or training. This range may be modified in the future.
All qualified applicants are considered for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, veteran status or other protected class.
Read our Job Applicant Privacy Policy
Seniority level
Seniority levelMid-Senior level Employment type
Employment typeFull-time Job function
Job functionInformation Technology Referrals increase your chances of interviewing at Mirador Therapeutics by 2x Sign in to set job alerts for “Associate Technical Director” roles. San Diego, CA $170,000.00-$210,000.00 10 hours ago Senior Project Manager, Customer ExperienceSupply Chain Manufacturing Operational Excellence TPM/IWS - Manager - Consulting - Location OPENSr. Software Engineer - Payments Support San Diego, CA $80,000.00-$110,000.00 6 hours ago Sr. Software Engineer - Investment ManagerSenior Software Engineer – SOC Power/Thermal software - AutomotiveHydraulic Modeling & Analysis - Senior Project Manager - Water, Wastewater & Recycled Water (Option for Remote)Senior Software Engineer – Localization and State Estimation (R3123)Senior Project Manager- Water Conveyance/Pump StationsSenior Program Project Manager (Exp in Regulatory or Medical Device Industry)Senior Project Manager - Transmission Routing and SitingSr. Project/Program Manager (Min 5 Yrs. Healthcare Exp.)Associate Technical Director - Bridge, for COWI in North AmericaSenior Principal Embedded Software Engineer -Onsite (Strong C++ & real-time/embedded systems area)Automotive - Platform Software Engineer (Staff-Sr. Staff Position)Senior or Software Technical Product Manager 2 (Engineering)Senior Systems Engineer – Software Focus (Remote / Flexible) San Diego, CA $126,536.00-$161,684.00 9 hours ago Sr. Superintendents, Project Managers, Sr. Projects EngineersSenior Project Manager - up to $190K (Educational Exp*) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr