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Director Formulation Development Jobs in Wisconsin

... formulation compliance risks. · Provides regulatory guidance during product development, commercialization, and change implementation. DIRECT REPORTS This role does not have direct reports.

WI · On-site

$170 - $180/hr

Success is defined by the development of growing pipeline of partners and the launch of new markets ... formulation and execution, financial analysis and reporting, accounts receivable/payable, and ...

Rubber Compounding Chemist

Rochester, WI · On-site

$90K - $120K/yr

Join a stable, long-established manufacturer where you'll have a direct impact on developing and ... product development Design and execute laboratory experiments, including formulation and testing ...

... D formulation and high-volume production. This role provides hands-on leadership for all batching ... Direct oversight of thermal lethality processes, ensuring all CCPs are monitored, documented, and ...

WI · On-site

$70 - $100/hr

... formulation excipients and nanoparticles, you will play a direct role in generating the analytical evidence that supports the development of future medicines. From early research activities through ...

New

Acts as a catalyst for change by guiding and directing organizational design, development, and ... formulation of associate development plans, identify critical positions and develop succession ...

Acts as a catalyst for change by guiding and directing organizational design, development, and ... formulation of associate development plans, identify critical positions and develop succession ...

Showing results 21-40

Director Formulation Development information

What is a Director Formulation Development?

A Director of Formulation Development leads the design and optimization of pharmaceutical formulations, ensuring they meet quality, regulatory, and performance standards. They oversee research, guide teams in developing new drug delivery systems, and collaborate with regulatory and manufacturing teams. This role requires expertise in chemistry, pharmaceutics, and process development to ensure successful product commercialization. Additionally, they manage project timelines, budgets, and technical challenges to drive innovation in drug formulation.

What does a Director Formulation Development do?

As a Director Formulation Development, you will oversee the design and optimization of drug formulations, lead a multidisciplinary team of scientists, and ensure that projects meet quality, budget, and timeline expectations. Your daily activities often include strategic planning, reviewing progress reports, troubleshooting formulation challenges, and collaborating with regulatory, manufacturing, and quality assurance departments. You may also interact with upper management to report on key milestones and contribute to long-term product development strategies. This role offers opportunities to influence project pipelines and play a central part in bringing new therapies to market.

What are the key skills and qualifications needed to thrive as a Director Formulation Development?

A Director Formulation Development typically requires an advanced degree in pharmaceutical sciences, chemistry, or a related field, along with significant experience in drug formulation and team management. Familiarity with industry-standard formulation software, regulatory compliance systems, and relevant certifications such as PMP or Six Sigma are highly valued. Excellent leadership, communication, and strategic planning skills help set high performers apart in this role. These skills and qualities are critical for driving innovative product development, ensuring regulatory compliance, and effectively leading cross-functional teams.

What are popular job titles related to Director Formulation Development jobs in Wisconsin?

For Director Formulation Development jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Director Formulation Development jobs in Wisconsin look for?

The top searched job categories for Director Formulation Development jobs in Wisconsin are:

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Cities in Wisconsin with the most Director Formulation Development job openings:

Label Compliance Specialist

Sartori

Plymouth, WI • Hybrid

Full-time

Re-posted 14 days ago


Sartori Cheese rating

5.6

Company rating: 5.6 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

361st of 440 rated food and drinks producers


Job description

SUMMARY

The Label Compliance Specialist supports regulatory compliance for product labeling, ingredient statements, nutrition facts, claims, and formulations in alignment with FDA regulations (21 CFR Part 101) and applicable certification standards. This role partners with R&D, Marketing, Quality, and Supply Chain to support compliant product development and commercialization while serving as a technical resource for labeling, claims, and ingredient compliance.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

Labeling & Claims Compliance

· Reviews and approves product labels to ensure compliance with FDA labeling regulations, including nutrition facts, ingredient statements, allergen declarations, and required statements.

· Reviews and assesses on-pack and marketing claims (e.g., “natural,” “non-GMO,” “free from”) for regulatory and certification compliance.

· Supports the development, maintenance, and organization of claim substantiation documentation.

· Ensures label updates are completed accurately and within established timelines.

Ingredient & Formulation Compliance

· Reviews ingredients, formulations, and specifications for compliance with FDA regulations, GRAS status, food additive approvals, and customer requirements.

· Assesses supplier documentation and regulatory status of raw materials.

· Supports change management activities related to ingredient, formulation, or specification updates.

· Maintains ingredient and formulation compliance records and documentation.

Certification & Audit Support

· Ensures assigned products meet requirements for applicable certifications (e.g., Non-GMO, Kosher, Halal).

· Coordinates product-level documentation for certification bodies.

· Supports certification audits and tracks assigned corrective actions.

Regulatory Monitoring & Cross-Functional Support

· Monitors applicable domestic and international labeling regulations and supports awareness of emerging requirements.

· Collaborates with internal partners and external resources to identify and address labeling and formulation compliance risks.

· Provides regulatory guidance during product development, commercialization, and change implementation.

DIRECT REPORTS

This role does not have direct reports.

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

EDUCATION AND EXPERIENCE

· Bachelor’s degree in science, business, or another related field required.

· Minimum of 3-5 years of food regulatory experience required.

· Experience supporting domestic and international food regulations, required.

· Experience working with product information and manufacturing systems (e.g., PLM, ERP, Genesis), required.

· Experience supporting certification or claim programs (e.g., Non-GMO, Kosher, Halal), preferred.

OTHER KNOWLEDGE, SKILLS, AND ABILITIES

· Judgment: Forms sound opinions and make solid decisions.

· Ethical: Acts with integrity and aligns behavior to organizational values.

· Quality Commitment: Consistently strives to meet high standards of excellence.

· Collaborative: Partners with others to realize better results.

· Customer Focused: Understands and responds effectively to stakeholder needs.

· Problem Solver: Identifies root causes and recommends effective solutions.

· Detail-oriented: Ensures accuracy and precision in work output.

· Organized: Structures work and information in a logical, efficient, manner.

· Prioritizes Effectively: Identifies and focuses on the most critical responsibilities.

CERTIFICATIONS

None.

ADDITIONAL INFORMATION

WORK LOCATION

This role is expected to be onsite at our Pleasant View location in Plymouth, WI 3 days per week and may work remotely 2 days per week. Remote work must be performed within Wisconsin or another approved state in accordance with company policy.

TRAVEL REQUIREMENTS

Occasional Travel (up to 10%) – Limited travel for training, meetings, or visits to other Sartori manufacturing facilities.

PHYSICAL DEMANDS

The physical demands described here are representative of those that must be met by a Team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

The role requires extended periods of sitting. The role may involve lifting or carrying up to 10 pounds. The role requires repetitive hand or arm movements and sustained use of hands or arms. The role requires the ability to see details at close range and communicate verbally.

WORK ENVIRONMENT

The work environment characteristics described here are representative of those a Team Member encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

This role is primarily performed in an office or administrative environment. The work environment is generally quiet to moderate in noise level.

The above statements are intended to describe the general nature and level of work being performed by Team Members assigned to this work. This is not an exhaustive list of all duties and responsibilities. Sartori Company reserves the right to amend and change responsibilities to meet organizational and business needs as necessary.


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