What are the responsibilities and job description for the Manager, Regulatory Operations position at Mannkind Corporation?

Position: Manager, Regulatory Operations

Location:

Burlington, MA

Job Id: 112770

# of Openings: 1

Company Overview

MannKind Corporation (Nasdaq: MNKD) is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient-centric solutions. With a focus on cardiometabolic and orphan lung diseases, we develop and commercialize treatments that address serious unmet medical needs, including diabetes, pulmonary hypertension, pulmonary fibrosis, nontuberculous mycobacterial (NTM) lung disease, and fluid overload associated with heart failure and chronic kidney disease.

At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.

Position Summary

The Regulatory Operations Manager will play a critical role in planning, preparing, and managing global regulatory submissions, with a strong emphasis on eCTD publishing and lifecycle management. This individual will ensure submissions are compliant, highquality, and delivered on time to global health authorities. The role requires close collaboration with crossfunctional partners-including Regulatory Affairs, CMC, Clinical, and Quality-to support regulatory strategy and execution across development programs.

Key Responsibilities

Submission Planning & Management

Lead the endtoend planning, coordination, and execution of global regulatory submissions (IND/CTA, NDA/MAA, amendments, supplements, responses to queries, and annual reports).
Develop and maintain submission timelines, deliverable trackers, and communication plans to ensure alignment across functional teams.
Serve as the primary internal point of contact for submissionrelated activities and issue resolution.

eCTD Publishing & Lifecycle Management

Prepare, compile, and publish electronic submissions in eCTD format in accordance with regional requirements (FDA, EMA, Health Canada, PMDA, and other global authorities).
Manage submission lifecycle activities, including sequence planning, metadata management, and archive maintenance.
Ensure submissions meet all technical standards, validation criteria, and regulatory guidance.

Compliance & Quality

Maintain uptodate knowledge of global electronic submission standards, regulatory requirements, and industry best practices.
Oversee document formatting, QC, and version control to ensure accuracy and consistency.
Support inspection readiness and contribute to continuous improvement of regulatory operations processes, templates, and systems.

CrossFunctional Collaboration

Partner closely with Regulatory Strategy Teams to support and ensure alignment on submission content and timelines.
Work with Product Development (CMC and Device), Clinical, Manufacturing, Nonclinical, and Quality teams to coordinate document delivery and resolve content or formatting issues.
Provide guidance to authors on document standards, templates, and submission expectations.

Required Qualifications

Bachelor's degree preferably in a scientific or technical discipline.
7 years of experience in Regulatory Operations within the pharmaceutical or biotechnology industry.
Demonstrated expertise in global eCTD publishing, including handson experience with major publishing tools and validation software.
Strong understanding of global regulatory requirements and electronic submission standards (FDA, EMA, ICH, etc.).
Proven ability to manage multiple submissions and deadlines in a fastpaced environment.
Excellent organizational skills, attention to detail, and communication abilities.

Preferred Experience

Experience supporting major submissions such as IND, NDA, BLA, or MAA.
Familiarity with regulatory information management systems (RIMS) and document management systems (DMS).
Knowledge of emerging global electronic submission requirements (e.g., eCTD 4.0).
Prior experience in a midsized or rapidly growing biotech/pharma environment.
Project management training or certification.

Pay Range: $116,000 - $174,000 per hour

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Mannkind Corporation is proud to be an Equal Employment Opportunity employer. We provide equal employment opportunity (EEO) to all persons regardless of race, creed, color, religion, national origin, ancestry, gender (including pregnancy, breastfeeding or medical condition related to pregnancy or breastfeeding), age, physical or intellectual disability, sexual orientation, gender identity, gender expression, gender stereotyping, marital status, military or veteran status, citizenship, genetic characteristic or information, or any other characteristic protected by applicable federal, state, or local law.

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