ZipRecruiter

Log In

1

Dossier Jobs (NOW HIRING)

Airbus

Process Engineer

Kinston, NC · On-site

Primary Responsibilities: 1. Process Optimization: (45%) • Ensure the industrial feasibility of the Definition Dossier. • Create and maintain an Integrated Manufacturing Dossier from the ...

Matmut

Vos missions contacter les victimes, leurs ayants droit ou leurs mandataires en vue de la constitution de leur dossier (justificatifs des prejudices, remise des documents reglementaires, etc.), les ...

Expleo

ingenieur methodes

Los Angeles, CA

$91K - $113K/yr

Definir le dossier de fabrication (Gammes, nomenclatures, FI, programmes, STL) et participer a l'elaboration du dossier de controle * Etablir et suivre les couts recurrents et non recurrents de ...

Expleo

ingnieur mthodes

Los Angeles, CA · On-site

Définir le dossier de fabrication (Gammes, nomenclatures, FI, programmes, STL) et participer à l'élaboration du dossier de contrôle * Etablir et suivre les coûts récurrents et non récurrents ...

next page

Showing results 1-20

All JobsDossier Jobs

Dossier information

See salary details

$567

$1K

$1.7K

How much do dossier jobs pay per week?

As of Jul 14, 2026, the average weekly pay for dossier in the United States is $1,017.23, according to ZipRecruiter salary data. Most workers in this role earn between $807.69 and $1,173.08 per week, depending on experience, location, and employer.

Is Dossier a legitimate company?

Dossier is a company that offers employment screening and background check services, often used by employers to verify candidate information. It is a legitimate business operating within the background screening industry, and its services are widely recognized and utilized by various organizations. Job seekers should ensure they are applying through official channels and verify any employment offers independently.

What is the difference between Dossier vs Case Manager?

AspectDossierCase Manager
Required CredentialsTypically requires a high school diploma or equivalent; some roles may need certifications in record managementRequires a bachelor's degree in social work, healthcare, or related fields; certifications may be preferred
Work EnvironmentOffice settings, record storage facilities, administrative environmentsHealthcare facilities, social service agencies, client-facing settings
Employer & Industry UsageUsed mainly in legal, administrative, and record-keeping contextsCommon in healthcare, social services, and community support industries

While both roles involve managing information, a Dossier focuses on organizing and maintaining records, whereas a Case Manager actively coordinates services and supports clients' needs. Understanding these differences helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a Dossier Manager, and why are they important?

To excel as a Dossier Manager, you need expertise in document management, regulatory compliance, and strong organizational skills, often backed by a degree in life sciences or a related field. Familiarity with electronic document management systems (EDMS), regulatory submission platforms, and industry-specific standards like eCTD is crucial. Attention to detail, effective communication, and project management abilities are key soft skills that enhance performance in this role. These skills ensure accurate, timely, and compliant dossier submissions, which are critical for regulatory approval and company success.

What jobs make $1,000,000 a year?

High-level executive roles such as CEOs, CFOs, and other C-suite positions in large corporations often earn over $1 million annually, especially with bonuses and stock options. Additionally, successful entrepreneurs, top-tier investment bankers, hedge fund managers, and certain professional athletes or entertainers can reach this income level, often requiring extensive experience, specialized skills, and significant responsibility.

What are some common challenges faced by professionals responsible for managing dossiers, and how can they be addressed?

Professionals managing dossiers often encounter challenges such as maintaining accurate and up-to-date documentation, ensuring compliance with regulatory standards, and coordinating information from multiple stakeholders. Staying organized and implementing robust document management systems can help mitigate these issues. Additionally, clear communication with cross-functional teams and ongoing training on regulatory changes are essential for staying compliant and efficient in this role.

What is a dossier in a professional context?

A dossier is a collection of documents, records, or information compiled about a specific person, subject, or project. In professional settings, dossiers are used to organize and present comprehensive information for decision-making, evaluations, or reporting. They can include resumes, reports, references, and other relevant materials, depending on their purpose. Dossiers are commonly used in fields like law, healthcare, business, and government to ensure all pertinent information is easily accessible and well-organized.

What jobs pay 500,000 a year in the US?

In the US, high-paying roles such as senior executives (CEOs, CFOs, COOs), successful entrepreneurs, and certain specialized medical professionals can earn $500,000 or more annually. These positions often require extensive experience, advanced degrees, strong leadership skills, and sometimes ownership stakes or performance-based bonuses.

What is a job Dossier?

A job dossier is a comprehensive collection of a candidate's professional documents, including resumes, cover letters, certifications, and work samples, used to showcase qualifications for a specific position. It helps employers evaluate a candidate's skills, experience, and suitability for the role. Preparing a well-organized dossier can improve the chances of securing an interview.
More about Dossier jobs
What cities are hiring for Dossier jobs? Cities with the most Dossier job openings:
What states have the most Dossier jobs? States with the most job openings for Dossier jobs include:
What job categories do people searching Dossier jobs look for? The top searched job categories for Dossier jobs are:
Dossier jobs near you
Infographic showing various Dossier job openings in the United States as of July 2026, with employment types broken down into 88% Full Time, 9% Part Time, 2% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $52,896 per year, or $25.4 per hour.
Director, Regulatory Affairs (Global Filing Lead)

Director, Regulatory Affairs (Global Filing Lead)

Revolution Medicines

Redwood City, CA • On-site

$183K - $242K/yr

Full-time

Re-posted 26 days ago

Job description

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
The Director of Regulatory Affairs (Global Filing Lead) is accountable for driving preparation & execution of global regulatory NDA/MAA filings for late-stage oncology programs at RevMed. They will manage end-to-end execution of the dossier, ensuring cross-functional coordination and effective communication across Regulatory, Clinical, Biostatistics, CMC, Quality, Translational Medicine and Commercial. The Director will support drug development teams and ensure delivery of targeted, pragmatic, well-vetted, consistent and actionable regulatory advice. The Director must have a thorough understanding and be highly experienced in oncology drug development, US NDA & global filing regulations, current Health Authority thinking, and have strong leadership & problem-solving ability.
Reports into Regulatory Affairs, Global Filing & Registration
  • High-Impact position to lead cross-functional development & regulatory submission activities for registrational oncology programs in the EU, UK, Japan and internationally.
  • Collaborate closely with Program Teams and Global Regulatory Leads to advance effective & consistent regulatory strategies to enable successful filing of approval of New Drug Applications.
  • Develop strategic filing plans under expedited regulatory pathways, programs and developing Health Authority initiatives.
  • Coordinate dossier filing and sub-team rosters for management endorsement.
  • Lead cross-functional MAA kickoff according to global filing plans and framework.
  • Maintain & track an integrated filing plan including regulatory timelines, modular MAA deliverables, critical path activities, in concert with Regulatory Program Management.
  • Identify, respond to, and proactively mitigate risks to filing timelines or regulatory outcomes and report progress to senior management.
  • Drive and/or support modular NDA Sub-teams (e.g., across Clinical, Non-Clinical, Product Label, etc.) to ensure consistent communication, timely data delivery, and issue resolution.
  • Lead relevant Health Authority meetings, interactions and query responses and coordinate cross functional team preparation & involvement.
  • Motivate, mentor and develop direct reports to ensure development and performance.

Required Skills, Experience and Education:
  • Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 12 years in the pharmaceutical/biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including a regulatory strategy role.
  • Proven success in executing global NDA/MAAs (preparation, submission & approval).
  • Experience filing applications under expedited filing pathways and programs to enable fastest possible regulatory approval.
  • Demonstrated ability to lead Health Authority interactions and negotiations.
  • In-depth knowledge of CTD structure and management of dossier components.
  • Direct experience in oncology drug development including oversight of large, global Phase 3 registrational studies.
  • Flexibility to support business needs of dynamic registrational programs.
  • Skilled at representing Regulatory on cross-functional teams and presenting to senior leadership.
  • Excellent communication, planning, and organizational skills with the ability to manage multiple projects and tight deadlines.

Preferred Skills:
  • Prior experience with regulatory filings and strategy in APAC and access consortium countries highly preferred.
  • An advanced degree is desirable.
    #LI-Hybrid #LI-SH1

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$211,000-$264,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

Apply