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Remote Director Formulation Development Jobs in Reading, MA

Vrtx

HEOR Modeling Director (Remote-Eligible)

Boston, MA · On-site +1

$204K - $306K/yr

Lead the development of global cost-effectiveness and budget impact models, and associated ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

FortifyIQ

Sales Director (Remote)

Salem, MA · Remote

We're seeking an accomplished Sales Director to lead growth initiatives across global regions ... Develop and execute business development and sales strategies for assigned territories. * Manage ...

Vrtx

Associate Director, Audit Management

Boston, MA · Remote

$154K - $231K/yr

Contributes to the development and maintenance of the integrated and risk-based GxP Audit Plan and ... Remote-Eligible Flex Eligibility Status: In this Remote-Eligible role, you can choose to be ...

Oscar Health

Associate Director, Tax

Boston, MA · Remote

$162K - $213K/yr

This is a remote position, open to candidates who reside in: Boston, MA. You will be fully remote ... Stay abreast and educate others on developments within the insurance tax area and their possible ...

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Remote Director Formulation Development information

See Reading, MA salary details

$93.9K

$202K

$303.4K

How much do remote director formulation development jobs pay per year?

As of Jun 7, 2026, the average yearly pay for remote director formulation development in Reading, MA is $201,976.00, according to ZipRecruiter salary data. Most workers in this role earn between $99,200.00 and $262,700.00 per year, depending on experience, location, and employer.

What does a Remote Director of Formulation Development do?

A Remote Director of Formulation Development leads and manages the development of new pharmaceutical or chemical formulations while working off-site. This role involves overseeing teams of scientists, coordinating research and development projects, ensuring regulatory compliance, and collaborating with cross-functional teams to bring new products from concept to market. The director is also responsible for setting project timelines, allocating resources, and solving complex formulation challenges. Working remotely, they use digital tools to communicate, monitor progress, and ensure all formulation activities align with company objectives and quality standards.

What are the key skills and qualifications needed to thrive as a Remote Director of Formulation Development, and why are they important?

To thrive as a Remote Director of Formulation Development, you need advanced expertise in pharmaceutical sciences, chemistry, or chemical engineering, often supported by a PhD or master's degree and substantial industry experience. Proficiency with formulation development software, regulatory requirements (like FDA or EMA guidelines), and project management systems is typically required. Strong leadership, strategic thinking, and effective communication are critical soft skills for managing remote teams and cross-functional projects. These competencies ensure the timely and compliant development of pharmaceutical formulations while maintaining high standards and fostering innovation.

What is the difference between Remote Director Formulation Development vs Remote Formulation Scientist?

AspectRemote Director Formulation DevelopmentRemote Formulation Scientist
CredentialsAdvanced degrees (PhD, MS) in pharmaceutical sciences or related fields, extensive industry experienceBachelor's or Master's in pharmaceutical sciences, chemistry, or related fields, with relevant experience
Work EnvironmentLeadership role overseeing teams, strategic planning, cross-department collaborationHands-on laboratory work, experimental design, data analysis
Employer & Industry UsagePharmaceutical and biotech companies, contract research organizationsPharmaceutical companies, research labs, biotech firms

The Remote Director Formulation Development typically holds a senior leadership position, focusing on strategic oversight and team management, while the Remote Formulation Scientist is more involved in experimental work and data generation. Both roles require relevant scientific credentials, but the director role emphasizes leadership and project management.

How does a Remote Director of Formulation Development typically collaborate with cross-functional teams given the virtual work environment?

As a Remote Director of Formulation Development, you will frequently coordinate with R&D, quality assurance, regulatory, and manufacturing teams across different locations. Effective communication is key, with regular video conferences, project management tools, and shared digital platforms used to ensure alignment on project goals and timelines. While remote work offers flexibility, it also requires proactive engagement to foster collaboration, resolve challenges quickly, and maintain team cohesion. You'll often lead virtual meetings, provide feedback on technical reports, and guide your team through complex formulation projects from concept to commercialization.
What job categories do people searching Remote Director Formulation Development jobs in Reading, MA look for? The top searched job categories for Remote Director Formulation Development jobs in Reading, MA are:
What cities near Reading, MA are hiring for Remote Director Formulation Development jobs? Cities near Reading, MA with the most Remote Director Formulation Development job openings:
Remote Director Formulation Development jobs near you
Infographic showing various Remote Director Formulation Development job openings in Reading, MA as of May 2026, with employment types broken down into 75% Full Time, 15% Part Time, and 10% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $201,976 per year, or $97.1 per hour.

Associate Director, Market Access Operations

MannKind Corporation

Burlington, MA • On-site, Remote

$148K - $222K/yr

Full-time

Posted 19 days ago

Job description

MannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions, developing and commercializing innovative inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases. The company applies deep expertise in formulation science and inhalation‑device engineering to reduce the treatment burden for conditions such as diabetes, congestive heart failure, pulmonary fibrosis, and pulmonary hypertension.

MannKind’s core technologies, including ultrafine dry‑powder formulations and advanced inhalation platforms, enable rapid, convenient delivery of medicines directly to the deep lung. This approach supports both local pulmonary targeting and systemic delivery for various medical indications. Through alternative drug formulations and delivery mechanisms, MannKind aims to bring forward differentiated, patient‑centric therapies that expand treatment options to improve outcomes across chronic and rare diseases.
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:
MannKind Corporation currently has an open position for an Associate Director, Market Access Operations to support our Market Access team including departmental reporting and data analytics, government reporting, trade, payer contracting, and pricing analysis. This position will support Furoscix®, Afrezza®, V-Go®, and any future products and will collaborate broadly with Market Access, Finance, Legal, Supply Chain, Business Analytics, and Sales.

This position can be remote or hybrid in Burlington, MA, or Westlake Village, CA with occasional travel required. This position reports to the Executive Director - Government, Contracting and Trade.
Principal responsibilities will include:
The role functions as an expert in data modeling and reporting with meticulous attention to detail.
  • Lead the monthly reconciliation of source data used in government pricing calculations; sales, rebates, chargebacks, discounts and fees.
  • Perform parallel GP calculations and maintain forecast models for pricing analysis
  • Review vendor materials and validate BP, AMP, PHS/340B, NFAMP, FCP/FSS, IFF, and URA; ensure reports are submitted in accordance with government regulations.
  • Maintain company’s government portal registrations annually or as needed (SAM, CMS, TRICARE, etc.)
  • Ensure Public Law reporting, RFMs are accurate and deadlines are met
  • Review and maintain accurate customer Class of Trade assignments
  • Ensure all statutory pricing is up to date and accurate in the necessary government portals and assist in updating Compendia as needed
  • Work with department lead to continuously monitor US pricing and government program developments such as IRA and MFN. develop subject matter expertise and thought leadership in government program regulations at the Federal and State levels
  • Ability to analyze payer data to create insightful trend analysis and reports
  • Assist in contract review, analysis, and organization/tracking of key terms, timelines, and bid cycles
  • Familiar with Gross-to-Net and accounting principles. Will work with department lead to develop expertise and ability to model net sales forecast scenarios
  • Monitor and report on trends for all discounts, performance to contract, and channel mix
  • Work closely with the Corporate Account Directors on account setup and sales reporting
  • Work effectively amp; collaboratively with internal and external cross-functional partners, including pricing/contracting vendors, specialty pharmacies, IDNs, 3PL and other distribution partners
  • Create and maintain departmental dashboards to disseminate essential information throughout the organization.
  • Manage various trackers to record program data enhancements and data deliverables.
  • Participate in weekly vendor calls and quarterly business reviews
  • Support ongoing Market Access integration activities related to the acquisition of scPharma; vendor assessments, consolidation, unified financial and performance reporting across all brands
This role will also liaise with Legal/Regulatory/Compliance to ensure all operations, processes, and systems meet legal and regulatory requirements.
Education and Experience Qualifications:
  • ​Bachelors degree required
  • Minimum 7 years in the Biopharmaceutical industry, in analytics and/or reporting roles
  • Minimum 5 years of government pricing or relevant commercial finance experience
  • Minimum 3 years managing external vendor or client relationships
  • Ability to read and interpret complex contracts
  • Data Analysis and Vendor Management experience are required
  • Strong oral, written presentation skills, with ability to simplify complex concepts verbally or visually via PowerPoint and/or Excel (including pivot tables)
  • Technically savvy with proven cross-functional collaboration and teamwork
  • Ability to pivot quickly and operate through ambiguity
  • Strong strategic, analytical, time management, and multi-tasking abilities
  • Excellent data gathering, analytical and problem-solving skills
  • Proactive stakeholder engagement and management to prioritize analytics needs to enable data driven commercial decision-making process.
  • Strong analytics and project management skills to turn unstructured business issues into action plans that result in meaningful strategic or tactical recommendations
  • Behaves with high level of autonomy – identifies and challenges needs, acting accordingly initiating projects with impact on business outcomes
  • Solution-oriented strategic thinker with strong emotional intelligence

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