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Jobs at Celcuity (Now Hiring) — 3 open

Celcuity logoCelcuity

Senior Scientist, Formulation and Process Development

Remote OK

$150k–$175k/yr

Senior$1.6B raised

Position Summary: We are seeking a Senior or Principal Scientist, Formulation and Process Development, who will report to the Director, Pharmaceutical Development. You will focus on leading formulation and process develo…

Skills: Formulation Development, Process Development, Drug Product Development, Small Molecule Drugs, Sterile Parenteral Dosage Forms

Celcuity logoCelcuity

Bioinformatics Scientist

Plymouth, Minnesota, United States · On-site

$110k–$120k/yr

Senior$1.6B raised

Position Summary: Reporting to the Bioinformatics Senior Principal Investigator, the Bioinformatics Scientist will focus on complex experimental and clinical bioinformatics data sets. Responsibilities: Strong background …

Skills: Bioinformatics, R, Python, Multi-omics Analysis, Data Science

Celcuity logoCelcuity

Director, National Accounts and Field Reimbursement

San Francisco, California, United States · Remote OK

$230k–$250k/yr

Senior+$1.6B raised

Candidates located in California are preferred. Position Summary: We are seeking a Director of National Accounts and Field Reimbursement who will support the execution of market access strategies for Celcuity’s first com…

Skills: Market Access Strategy, Field Reimbursement, Payer Account Engagement, Oncology Product Support, Project Management

Celcuity logo

Senior Scientist, Formulation and Process Development

Celcuity

Remote OK

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Senior

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  • $150k–$175k/yr
  • Full-time
  • bachelor degree, postgraduate degree
  • Medical Insurance, Dental Insurance, Vision Insurance, 401(k) Match, Paid Time Off, Paid Holidays
  • Posted 7d ago
  • ~40 hrs/week

Responsibilities

Lead formulation and process development projects for novel and existing drug products throughout their lifecycle, from pre-formulation to manufacturing scale-up. Manage outsourced experiments at contract laboratories and CDMOs while serving as a subject matter expert for the broader team.

Requirements

Requires a degree in Pharmaceutical Science, Chemical Engineering, or a related field with at least 7 years of pharmaceutical development experience. Expertise in sterile parenteral dosage forms and poorly water-soluble APIs is highly preferred.

Full job description

Position Summary:

We are seeking a Senior or Principal Scientist, Formulation and Process Development, who will report to the Director, Pharmaceutical Development. You will focus on leading formulation and process development work supporting Celcuity’s drug product development and product lifecycle management. The Sr./Principal Scientist role will join a collaborative Pharmaceutical Development group focused on advancing Celcuity’s lead drug candidates. The Sr./Principal Scientist will lead formulation and process development projects for novel formulations targeted toward existing and new indications, as well as projects supporting Celcuity’s existing oncology drug product.

Responsibilities:

  • Lead projects to support development of novel and existing formulations, spanning the product lifecycle including pre-formulation, dosage form selection, formulation development, process development, and manufacturing scale-up.
  • Design, execute, and interpret formulation and process development experiments in an outsourced environment at contract laboratories and CDMOs.
  • Identify and vet new contract organizations to support formulation and process development.
  • Help define & execute the project plans for formulation lifecycle management.
  • Support writing technical sections for intellectual property and regulatory filings.
  • Develop and maintain an in-depth knowledge of formulation development trends, techniques, and technologies.
  • Serve as a subject matter expert for formulation development within the Pharmaceutical Development group and the broader Celcuity team.
  • Summarize, document, and present information to subgroup, group, and cross-functional audiences.
  • Other duties as assigned.

Qualifications:

  • Ph.D/M.S./B.S. in Pharmaceutical Science, Chemical Engineering, Chemistry, Biochemistry, Biochemical Engineering, or related fields.
  • 7+ years of experience in pharmaceutical development (preferred 4+ years industry experience for Ph.D; 5+ years for M.S.; 7+ years for B.S.).
  • Demonstrated experience with formulation development and drug product development, preferably for small molecule drugs.
  • Deep understanding of formulation techniques & considerations for sterile, parenteral dosage forms. Knowledge of other dosage forms (e.g., for ophthalmic or oral) is beneficial.
  • Experience with drug device combination products for injectable drug products (e.g., prefilled syringes, autoinjectors) is preferred. Knowledge of other dosage form delivery techniques (e.g., for ophthalmic) is beneficial.
  • Technical expertise in formulation strategies and processes specifically tailored to poorly water-soluble APIs is preferred. Subject matter expertise in one or more of these areas is highly desirable:
    • Nano-milling and nanosuspension formulation.
    • Micro/nano-emulsions.
    • Salt formation and salt screening/selection.
    • Complexation and co-solvency using cyclodextrins or co-solvents.
    • Lyophilization
  • Experience with physicochemical characterization methods for drug substances and drug products.
  • Excellent written and verbal communication skills, with ability to influence and build credibility at all levels.
  • Strong interpersonal skills for interacting with colleagues across various levels and functions.
  • Attention to detail and ability to manage multiple processes and documentation requirements.
  • Strong technical and analytical skills with advanced knowledge in MS Office products.
  • Ability to work in a team or independently as required.
  • Outstanding organizational skills with the ability to prioritize.
  • Demonstrated independent and sound decision-making skills; ability to think critically and make decisions in a fast-paced environment.
  • Flexible and willing to learn; able to adapt to business and site needs in a dynamic environment.
  • Maintain a positive, approachable and professional attitude.

About Us:

Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies for the treatment of multiple solid tumor indications. The company was founded to develop a better way to treat the cellular drivers of tumor growth.

Our lead therapeutic candidate, gedatolisib, is an intravenously administered, potential first-in-class PI3K/AKT/mTOR (PAM) pathway inhibitor. Its mechanism of action and pharmacokinetic properties are highly differentiated from other currently approved and investigational therapies that target PI3K or mTOR alone or together. Gedatolisib phase 3 clinical development programs are focused on the treatment of patients with HR+/HER2- ABC in the 1L and 2L settings. A Phase 1b/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is on-going.

Celcuity is an Equal-Opportunity Employer.

Celcuity is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are competitive. For this role, the anticipated base pay range is $150,000 - $175,000 DOE. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.

The successful candidate will be eligible for an annual performance incentive bonus and a new hire equity package. Celcuity also offers various benefits offerings, including, but not limited to, medical, dental, vision insurance, 401(k) match, PTO, and paid holidays.

Notice to Recruiters/Staffing Agencies

Recruiters and staffing agencies should not contact Celcuity through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees directly.

We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file. Celcuity’s receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Celcuity and such organization and will be considered unsolicited. Celcuity will not be responsible for related fees.

Related keywords

Pharmaceutical DevelopmentDrug ProductSmall MoleculeParenteralOphthalmicOral DosagePrefilled SyringesAutoinjectorsAPICyclodextrinsCo-solvencyBiotechnologyOncologyPI3K/AKT/mTORClinical-stageCDMO

About Celcuity

LinkedInVisit site
Industry
Biotechnology
Company size
51-200 employees
Headquarters
Minneapolis, MN
LinkedIn followers
9,748
Total funding
$1.6B

Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies for the treatment of multiple solid tumor indications. The company was founded to develop a better way to treat the cellular drivers of tumor growth. Our lead therapeutic candidate, gedatolisib, is an intravenously administered, potential first-in-class PI3K/AKT/mTOR (PAM) pathway inhibitor. Its mechanism of action and pharmacokinetic properties are highly differentiated from other currently approved and investigational therapies that target PI3K or mTOR alone or together. Gedatolisib phase 3 clinical development programs are focused on the treatment of patients with HR+/HER2- ABC in the 1L and 2L settings. A Phase 1b/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is on-going. Celcuity is headquartered in Minneapolis. Further information about Celcuity can be found at www.celcuity.com

Offices: 16305 36Th Ave N, Minneapolis, MN 55446, US

Health DiagnosticsHealth CareBiotechnologyTherapeutics
View all jobs at Celcuity

About Celcuity

LinkedInVisit site
Industry
Biotechnology
Company size
51-200 employees
Headquarters
Minneapolis, MN
LinkedIn followers
9,748
Total funding
$1.6B

Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies for the treatment of multiple solid tumor indications. The company was founded to develop a better way to treat the cellular drivers of tumor growth. Our lead therapeutic candidate, gedatolisib, is an intravenously administered, potential first-in-class PI3K/AKT/mTOR (PAM) pathway inhibitor. Its mechanism of action and pharmacokinetic properties are highly differentiated from other currently approved and investigational therapies that target PI3K or mTOR alone or together. Gedatolisib phase 3 clinical development programs are focused on the treatment of patients with HR+/HER2- ABC in the 1L and 2L settings. A Phase 1b/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is on-going. Celcuity is headquartered in Minneapolis. Further information about Celcuity can be found at www.celcuity.com

Offices: 16305 36Th Ave N, Minneapolis, MN 55446, US

Health DiagnosticsHealth CareBiotechnologyTherapeutics
View all jobs at Celcuity

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