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Cmc In Biotech Jobs in Boston, MA (NOW HIRING)

Global Regulatory CMC Lead

Norwood, MA ยท On-site

$142K - $256K/yr

... in the pharmaceutical/biotech industry, manufacturing and/or analytical focus * 5+ years of experience in Biologics focused Regulatory CMC * Strong knowledge of current Global CMC regulations ...

Director, Regulatory Affairs CMC

Boston, MA ยท Hybrid

$190K - $285K/yr

The Director, Chemistry Manufacturing Controls (CMC) leads a Regulatory CMC team responsible for ... biotechnology company that invests in scientific innovation. Vertex is committed to equal ...

Showing results 41-60

Cmc In Biotech information

What is the difference between Cmc In Biotech vs Formulation Scientist?

AspectCmc In BiotechFormulation Scientist
Required CredentialsBachelor's or Master's in Life Sciences, Good Manufacturing Practice (GMP) knowledgeBachelor's or Master's in Pharmacy, Chemistry, or related field; GMP experience
Work EnvironmentLaboratories, manufacturing facilities, regulatory settingsLaboratories, R&D departments, manufacturing units
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract manufacturing organizationsPharmaceutical companies, biotech firms, contract labs

While both roles operate within the biotech and pharmaceutical industries, Cmc In Biotech focuses on Chemistry, Manufacturing, and Controls documentation and regulatory compliance, whereas Formulation Scientists primarily develop and optimize drug formulations. Cmc In Biotech professionals ensure regulatory submissions are complete, while Formulation Scientists work on creating effective drug delivery systems. Both roles often collaborate but serve distinct functions within the product development pipeline.

What is a CMC in biotech position?

A CMC (Chemistry, Manufacturing, and Controls) position in biotech involves overseeing the development, manufacturing, and quality control of biopharmaceutical products. Professionals in this role ensure that products meet regulatory standards and are produced consistently, often requiring knowledge of GMP (Good Manufacturing Practice) and regulatory guidelines.

What is a CMC in biotech?

In biotech, CMC stands for Chemistry, Manufacturing, and Controls, which refers to the detailed documentation and processes involved in developing, producing, and ensuring the quality of a biopharmaceutical product. CMC professionals are responsible for regulatory compliance, process validation, and quality assurance to meet industry standards and facilitate product approval.

What is the CMC in biotech?

In biotech, CMC stands for Chemistry, Manufacturing, and Controls, which refers to the detailed documentation and processes ensuring the quality, safety, and efficacy of a biotech product throughout development and production. Professionals in this field often work on regulatory submissions, quality assurance, and process validation to meet industry standards.

What are popular job titles related to Cmc In Biotech jobs in Boston, MA?

For Cmc In Biotech jobs in Boston, MA, the most frequently searched job titles are:

What cities near Boston, MA are hiring for Cmc In Biotech jobs?

Cities near Boston, MA with the most Cmc In Biotech job openings:

Senior Director, Biologics Drug Product Development and Manufacturing

Korsana Biosciences, Inc.

Waltham, MA โ€ข On-site

$260 - $360/hr

Other

Re-posted just now


Job description

Senior Director, Biologics Drug Product Development and Manufacturing

Korsana Biosciences, Inc. Waltham, Massachusetts, United States

About this positionAbout Us

Korsana Biosciences is a private biopharmaceutical company advancing a pipeline of potential best-in-class therapies for neurodegenerative diseases. In partnership with Paragon Therapeutics, we have developed Therapeutic Targeting (THETAโ„ข), a novel blood-brain barrier-penetrant shuttle platform designed to enable dramatically higher drug concentration inside the brain and overcome the limitations of earlier shuttle technologies. Our lead program is KRSA-028, an investigational, shuttled antibody targeting amyloid beta designed to be a best-in-class treatment for Alzheimerโ€™s disease. Our mission is to advance precision-engineered therapies, designed to address some of the biggest unmet needs in medicine. For more information, please visit www.korsana.com

Position Overview

The Senior Director, Biologics Drug Product Development and Manufacturing will provide program-specific leadership and subject matterexpertisefor biologicshigh-concentrationformulationand pre-filledsyringe(PFS)developmentand manufacturingin support of a best-in-class portfolio of preclinical and clinical programs.This leaderwill oversee the planning and execution of outsourceddrug product development and manufacturingactivities andwill work proactively with externalsuppliersincluding CDMOs and contract labsto define project scope, mitigate risks, and ensure successful deliverywith regard totechnical quality,timelinesand budget.Theincumbentwillcollaboratewithother functionsto deliver qualitydrugproducts for preclinical studies and clinical trials and Module 3 Quality for regulatory submission and approval. The position requires strategic vision and hands-on experience managing early-stage biotech programs in a dynamic, fast-paced environment.

Responsibilities
  • Establishes effective CMC strategies to develop biologics formulations, including high protein concentration formulations, and pre-filled syringe manufacturing process for a portfolio of biologics products in keeping with corporate and program objectives.
  • Collaborate with internal stakeholders in the areas of Analytical Development and Quality Control, Drug Substance Development, Combination Product Development, Clinical Supply Chain, Program Management, Preclinical Development, Clinical Development/Operations, Quality, Regulatory Affairs, and external business partners to push project forward.
  • Creates metrics for drug product function, monitors results and implements risk management strategies to address technical challenges and meet business goals.
  • Maintains an understanding of current trends and emerging biologics formulation and manufacturing technologies.
  • Provides clear communication to management regarding progress against technical objectives/milestones.
  • Ensures well-organized, clear and complete records of all activities across areas of responsibility.
Education & Experience
  • Ph.D. in (bio)chemistry, (bio)chemical engineering (or other relevant physical or life sciences discipline) or MS/BS with equivalent education or experience is required.
  • A minimum of 10 years of hands-on working experience in biologics drug product development in biotech or biopharma industry.
  • Experience in leading a cross functional CMC team is desired
  • Experience in a fast paced, high-growth startup environment is preferred
  • Experience in successful IND/IMPD/CTA submissions and approval
Skills & Attributes
  • Demonstrated ability in the areas of biologics high-concentration formulation and pre-filled syringe development, drug product manufacturing process development and characterization.
  • Expert knowledge of analytical methods used in the characterization of formulations for biologics and experience in advancing biologics drug product manufacturing processes through clinical development to successful regulatory approval.
  • Proven track record of CDMO management in supporting biologics drug product formulation, PFS development and GMP manufacturing.
  • Hands-on working experience of global CMC regulatory submission and approval.
  • Strategic thinker with a hands-on approach; comfortable balancing long-term planning with day-to-day execution
  • Exceptional communication and relationship-building skills, with the ability to influence across levels and functions
  • Strong attention to detail and problem-solving skills
  • Ability to distinguish between critical and non-critical priorities

Korsana Biosciences is the sixth groundbreaking company launched by Paragon Therapeutics, a premier biotech incubator founded by Fairmount Funds in 2021, known for its expertise in discovering and developing cutting-edge therapeutic assets in-house.

Korsana Biosciences is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status.

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