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Precision Biosciences Jobs (NOW HIRING)

Solid Biosciences

Scientist I, DTD

Charlestown, MA · On-site

$125K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Scientist I, Discovery & Translational Development - Solid Biosciences Charlestown, MA Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy ...

Cogent Biosciences

Senior Manager, Medical Information

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program ...

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How much do precision biosciences jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for precision biosciences in the United States is $16.59, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $16.83 per hour, depending on experience, location, and employer.

What are some common challenges faced by employees working at Precision Biosciences, and how does the company support professional growth?

Employees at Precision Biosciences often work at the forefront of gene editing technology, which can involve fast-paced projects and the need to adapt quickly to new scientific developments. Balancing innovation with regulatory compliance is a key challenge, as is collaborating across multidisciplinary teams. To support professional growth, Precision Biosciences offers opportunities for ongoing learning, mentorship, and clear pathways for advancement within both scientific and operational tracks. The company fosters a collaborative environment that encourages cross-functional teamwork and knowledge sharing.

What are the key skills and qualifications needed to thrive as a Precision Biosciences scientist?

To thrive as a scientist at Precision Biosciences, you typically need a strong background in molecular biology, gene editing, and cellular biology, supported by an advanced degree in a relevant scientific field. Experience with gene editing platforms like ARCUS, CRISPR, next-generation sequencing, and data analysis software is highly valued. Key soft skills include problem-solving, attention to detail, and effective teamwork and communication. These competencies are crucial for advancing innovative therapies, maintaining research accuracy, and collaborating efficiently in a fast-evolving biotechnology environment.

What is Precision Biosciences?

Precision Biosciences is a biotechnology company that specializes in developing genome editing technologies, with a focus on creating gene therapies for serious genetic diseases and cancer. Their proprietary ARCUS® genome editing platform allows for precise DNA editing, which can be used to develop innovative treatments. The company is involved in both in vivo gene editing programs and allogeneic cell therapies, aiming to address unmet medical needs and improve patient outcomes.

What is the difference between Precision Biosciences vs CRISPR Research Scientist?

AspectPrecision BiosciencesCRISPR Research Scientist
Primary RoleDevelops gene editing therapies using proprietary platformsConducts research and experiments using CRISPR technology
Work EnvironmentBiotech companies, laboratories, research institutionsAcademic labs, biotech firms, research institutions
Required CredentialsAdvanced degrees in molecular biology, genetics, or related fieldsMaster's or PhD in biology, genetics, or related disciplines
Industry UsageBiotech, pharmaceutical, gene therapy companiesResearch institutions, biotech startups, pharma companies

While both roles involve gene editing technologies, Precision Biosciences focuses on developing proprietary platforms for therapeutic applications, whereas CRISPR Research Scientists primarily conduct experiments and research using CRISPR tools. The roles often overlap in credentials and work environments, but their objectives differ—one is product development, the other research-focused.

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What states have the most Precision Biosciences jobs?

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Precision Biosciences jobs near you
Infographic showing various Precision Biosciences job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 10% Part Time, 3% Contract, and 2% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $34,500 per year, or $16.6 per hour.

Associate Director, Formulation Development

MBX Biosciences

Burlington, MA • On-site

Full-time

Re-posted yesterday

Job description

Position Summary
The Associate Director, Formulation Development will play a key role on MBX Biosciences' CMC team, supporting the development of peptide therapeutics across our pipeline.
Reporting into our Senior Director, Drug Product- this person will lead formulation design and optimization, oversee studies related to product quality and stability, and support development activities from early assessment through manufacturing transfer. The role requires strong scientific expertise in peptide or protein formulation development, collaboration across cross-functional teams and external partners, and a focus on advancing innovative therapies in a fast-paced biotech environment.
Key Responsibilities
  • Lead and contribute to the design, development, and optimization of pharmaceutical formulations for MBX's peptide therapeutics.
  • Oversee formulation development laboratory activities to support the advancement of peptide therapeutics across the MBX portfolio
  • Support implementation of analytical methods for characterizing peptides, including chromatographic techniques, spectroscopic techniques, and physical characterization in conjunction with AD
  • Oversee and ensure the implementation of robust QC procedures and ensure compliance with regulatory guidance and industry standards (e.g., ICH guidelines)
  • Plan and conduct non-GMP stability studies as part of formulation development. Contribute to the GMP stability study design to assess the shelf-life and degradation pathways.
  • Lead and contribute to the design and execution of drug product process optimization studies, to enhance product performance and manufacturability at scale. Contribute to the process transfer to CDMOs
  • Identify and address formulation and analytical technical challenges, e.g., through design experiments, root cause analyses, etc.
  • Partner effectively with MBX Regulatory personnel to ensure appropriate data, information, and documentation related to formulation and analytical methods are incorporated into regulatory documents
  • Other responsibilities as assigned

Education & Qualifications
  • Bachelor's, M.S or Ph.D. in pharmaceutical sciences, analytical chemistry, biochemistry, or related field with at least 8 years of relevant industrial experience, with a strong emphasis on formulation and analytical development
  • An in-depth understanding of peptide physicochemical stability, particularly for common routes of degradation, and direct experience in optimizing parenteral (liquid and lyophilized) formulations
  • Experience with combination products and devices is highly desirable
  • Hands-on experience with a variety of analytical methods, including SEC, RP-HPLC, LC-MS, and subvisible particle analysis
  • Prior experience in lyophilization formulation, cycle development, and analytical testing
  • Familiarity with end-to-end CMC drug development with an understanding of critical milestones and typical bottlenecks
  • CMC Regulatory knowledge, with a familiarity with regulatory requirements for parenteral drug products (e.g. FDA, EMA)
  • Highly motivated self-starter who works well both in teams as well as independently
  • Strong proven analytical and problem-solving abilities, with a track record of overcoming complex technical challenges in formulation and analytical development
  • Strong interpersonal & communication skills (written and oral), with the ability to develop strong collaborative working relationships with stakeholders and across technical functions, both internally and externally, to drive efficient execution of CMC technical development strategies
  • Strong organizational skills, ability to multi-task and work in a dynamic, fast-paced environment, with the ability to adapt to changing priorities and deadlines

Travel
You will be expected to travel periodically based on the needs of the business to the extent requested by the Company, including attendance at Together Weeks, Together Days, and functional meetings as requested by the Company.
Company Overview:
MBX Biosciences is a biopharmaceutical company focused on the discovery, development and commercialization of novel precision peptide therapies based on its proprietary PEP™ platform, for the treatment of endocrine and metabolic disorders. The Company is advancing a pipeline of novel candidates for endocrine and metabolic disorders with clinically validated targets, established endpoints for regulatory approval, significant unmet medical needs and large potential market opportunities. The Company's pipeline includes canvuparatide (MBX 2109) for the treatment of chronic hypoparathyroidism preparing for Phase 3 development; and an obesity portfolio that includes MBX 4291 in Phase 1 development and MBX 5765 in preclinical development, as well as additional discovery candidates. The Company is based in Carmel, Indiana and Burlington, Massachusetts. To learn more, please visit the Company website at www.mbxbio.com and follow it on LinkedIn.
EEO Statement:
MBX Biosciences is an Equal Opportunity Employer and is committed to treating all applicants fairly without discrimination. We welcome applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law.

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