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Remote Formulation Scientist Jobs in Massachusetts

Sail Biomedicines

Sr. Engineer, Drug Product

Cambridge, MA · On-site +1

$130K - $150K/yr

Position Summary We are seeking an Engineer / Scientist to support drug product process development ... Support process optimization and characterization activities for LNP formulation, TFF, mAb sterile ...

Calyx

Associate Scientist, Image Analysis

Needham, MA · On-site +1

$47K - $68K/yr

The Associate Scientist will communicate with the IA study lead on each study to understand the ... Fluent This role is remote. Candidates located in the following states: AZ, CT, DE, FL, GA, IL, MA ...

micro1 AI

Digital Chemistry Specialist - Remote

Boston, MA · Remote

$90 - $120/hr

Bioinformatics Scientist Role Type: Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their specialized expertise to a customer's innovative project. In this role ...

micro1 AI

Digital Chemistry Specialist - Remote

Quincy, MA · Remote

$90 - $120/hr

Bioinformatics Scientist Role Type: Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their specialized expertise to a customer's innovative project. In this role ...

micro1 AI

Digital Chemistry Specialist - Remote

Lowell, MA · Remote

$90 - $120/hr

Bioinformatics Scientist Role Type: Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their specialized expertise to a customer's innovative project. In this role ...

micro1 AI

Digital Chemistry Specialist - Remote

Lynn, MA · Remote

$90 - $120/hr

Bioinformatics Scientist Role Type: Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their specialized expertise to a customer's innovative project. In this role ...

Vrtx

MS&T Senior Manager - Drug Product

Boston, MA · On-site +1

$138K - $208K/yr

General Summary The Senior Manager, Manufacturing Science & Technology (MS&T) - Drug Product ... Provideonthefloorand remote MS&T support during manufacturing campaigns. * Partner with Operations ...

Gradient AI

Staff Data Scientist

Boston, MA · On-site +1

$160K/yr

This is a fully remote opportunity with hybrid available to those local to Boston. Gradient AI ... We are looking for a Staff Data Scientist to lead complex modelling and analytical projects of ...

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All JobsFormulation Scientist JobsRemote Formulation Scientist JobsRemote Formulation Scientist Jobs in Massachusetts

Remote Formulation Scientist information

What is the difference between Remote Formulation Scientist vs Remote Quality Control Analyst?

AspectRemote Formulation ScientistRemote Quality Control Analyst
Required CredentialsBachelor's/Master's in Chemistry, Pharmacy, or related field; experience in formulation developmentBachelor's in Chemistry, Biology, or related; experience in quality testing and analysis
Work EnvironmentLaboratories, R&D teams, pharmaceutical or biotech companiesLaboratories, manufacturing facilities, quality assurance teams
Industry UsagePharmaceutical, biotech, cosmetics, food industriesPharmaceutical, biotech, food, and consumer goods industries
Common Search/ComparisonYesYes

The Remote Formulation Scientist focuses on developing and optimizing product formulations, often working in R&D settings within pharmaceutical, biotech, or cosmetic industries. In contrast, the Remote Quality Control Analyst primarily conducts testing and analysis to ensure product quality and compliance. Both roles require relevant scientific credentials and are integral to product development and quality assurance processes in similar industries.

What are the most commonly searched types of Formulation Scientist jobs in Massachusetts? The most popular types of Formulation Scientist jobs in Massachusetts are:
What are popular job titles related to Remote Formulation Scientist jobs in Massachusetts? For Remote Formulation Scientist jobs in Massachusetts, the most frequently searched job titles are:
What job categories do people searching Remote Formulation Scientist jobs in Massachusetts look for? The top searched job categories for Remote Formulation Scientist jobs in Massachusetts are:
Remote Formulation Scientist jobs near you

Associate Director, Medical Writer

MannKind Corporation

Bedford, MA • On-site, Remote

$148K - $222K/yr

Full-time

Re-posted 24 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 is seeking a detail-oriented and highly organized Medical Writer to join our team. The Medical Writer will provide advanced scientific writing expertise and ensure the successful preparation of high-quality documents including but not limited to study protocols, CSRs, DSURS, IB, safety narratives, publications and submission documents. This role involves providing medical writing support for multiple compounds and projects within multiple therapeutic areas, potentially interfacing with external groups, and serving as the scientific writing expert for the department.
Essential Duties and Job Functions:
  • Coordinate and lead the review, approval, and production of writing projects, arranging and driving review meetings with cross-functional teams.
  • Ensure effective communication among project team members and contributors, holding them accountable to agreed-upon project dates.
  • Leads strategic document preparation for INDs, NDAs and briefing documents
  • Establish best practices, workflow infrastructure/templates, and standards to enhance consistency and quality across all regulatory and scientific documents.
  • Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.
  • Stay abreast of global regulatory requirements and guidelines (FDA, EMA, PMDA, ICH, etc.), ensuring company compliance and best practices.
  • Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing.
  • Lead and oversee medical writing project timelines, ensuring alignment with broader corporate milestones.
  • Serve as the medical writer representative on project teams.
  • Write and edit scientific, clinical, or abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives.
  • Complete reviews, quality checks and approvals.
  • Summarize results presented in graphical, tabular, and/or listing format.
  • Interpret complex clinical data and convert it into clear, concise, and engaging scientific content for diverse audiences.
Knowledge, Experience and Skills:
  • BS/BA +12 / MS/MBA 8-10, PhD 5+
  • Degree in science or medical related field. Master’s or PhD preferred.
  • Minimum of 7 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R amp;D.
  • Knowledge of US and international regulations, requirements, and guidance associated with writing projects.
  • Excellent written and oral communication skills, attention to detail, and ability to correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy.
  • Extensive experience working with collaborative, cross-functional teams
  • Develop and/or update document templates, work instructions, style guides, and department-related processes (SOPs)
  • Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred.
  • Understanding of publication/scientific communication guidelines.
  • Ability to provide strategic oversight while managing multiple priorities in a fast-paced environment.
  • Deep understanding of ICH-GCP guidelines and other relevant regulatory requirements.
  • Strategic thinker with strong execution skills.
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