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Telecommute Director Formulation Development Jobs in Minnesota

R&D Intern

Saint Paul, MN · On-site

$22 - $25/hr

... directors, and CEO. * Multiple networking, volunteer and fun events - both virtual and in-person ... raw materials, formulation principles, and structure-property relationships. * Synthesize and ...

R&D Intern

Saint Paul, MN · On-site

$22 - $25/hr

... directors, and CEO. * Multiple networking, volunteer and fun events - both virtual and in-person ... raw materials, formulation principles, and structure-property relationships. * Synthesize and ...

R&D Intern

Saint Paul, MN · On-site

$25/hr

... directors, and CEO. * Multiple networking, volunteer and fun events - both virtual and in-person ... raw materials, formulation principles, and structure-property relationships. * Synthesize and ...

Formulation, development, and implementation of accounting controls, procedures and policies ... The Finance Director supervises and is responsible for all accountants while they are performing ...

May interpret analytical data to guide formulation and process development decisions. ESSENTIAL ... and directing or participating as an active member of a work team. Promotes and supports the ...

New

... CDMO providing formulation development, clinical and commercial manufacturing, and packaging ... Self-directed, with sound judgment on compliance matters and a proactive approach to risk ...

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Telecommute Director Formulation Development information

What does a telecommute director formulation development do?

A Telecommute Director of Formulation Development oversees the design and improvement of pharmaceutical or chemical formulations while working remotely. This leadership role involves managing teams, coordinating cross-functional projects, ensuring regulatory compliance, and driving innovation in product development. They work closely with research, quality, and manufacturing departments to ensure products meet safety, efficacy, and quality standards, all while leveraging remote collaboration tools.

What are the key skills and qualifications needed to thrive as a telecommute director formulation development?

To thrive as a Telecommute Director Formulation Development, you need an advanced degree in pharmaceutical sciences or chemistry, extensive experience in drug formulation, and leadership in R&D. Proficiency with formulation software, regulatory submission platforms, and familiarity with GMP/GLP guidelines or certifications are typically required. Exceptional project management, communication, and cross-functional collaboration skills help drive virtual teams and align stakeholders. These competencies ensure effective formulation development, regulatory compliance, and successful product launches in a remote environment.

How does a telecommute director formulation development typically collaborate with cross-functional teams while working remotely?

A Telecommute Director of Formulation Development leverages digital collaboration tools to coordinate with R&D, regulatory, manufacturing, and quality assurance teams. Regular virtual meetings, project management platforms, and shared documentation ensure seamless communication and progress tracking. Despite working remotely, directors are expected to proactively facilitate brainstorming sessions, resolve issues in real time, and maintain clear communication channels to drive project milestones. Building strong relationships and fostering team engagement are crucial to successfully overseeing formulation projects from early development to scale-up.

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

AspectTelecommute Director Formulation DevelopmentTelecommute Formulation Scientist
CredentialsAdvanced degree (PhD or MS), extensive industry experienceBachelor's or Master's degree in Chemistry, Pharmacy, or related field
Work EnvironmentLeadership role overseeing teams and projects remotelyHands-on research and formulation work, often collaborative but can be remote
Industry UsageUsed in pharmaceutical and biotech companies for strategic formulation leadershipCommonly employed in R&D labs for developing formulations

The main difference is that the Telecommute Director Formulation Development focuses on leading formulation teams and strategic planning remotely, while the Telecommute Formulation Scientist is involved in hands-on formulation research and development. The director role requires more experience and leadership skills, whereas the scientist role emphasizes technical expertise in formulation science.

What cities in Minnesota are hiring for Telecommute Director Formulation Development jobs?

Cities in Minnesota with the most Telecommute Director Formulation Development job openings:

Senior or Principal Scientist, Formulation and Process Development

Minneapolis, MN

Linn Products, Inc
201 - 500 employees

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New


Job description

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.
  • Experience with preclinical study support and early-stage formulation development.
  • 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 commercial biotechnology company pursuing development of targeted therapies for treatment of multiple solid tumor indications. The company's first FDA-approved product is REVTORPYK (gedatolisib), a potent, pan-PI3K and mTORC1/2 inhibitor that comprehensively blockades the PAM pathway. REVTORPYK is approved to treat adults with HR+/HER2- advanced breast cancer that progressed on prior endocrine therapy in the metastatic setting.

The Phase 3 VIKTORIA-2 trial is evaluating gedatolisib in combination with palbociclib and either fulvestrant or letrozole for the first-line treatment of HR+/HER2- locally advanced or metastatic breast cancer. A Phase 1/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is ongoing.


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.