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Formulation Development Jobs in Indiana (NOW HIRING)

Astrix Inc

R&D Manager (OTC/Formulations)

Columbus, IN · On-site

Experience with product development or formulation chemistry * Familiarity with regulatory and quality compliance standards * Ability to manage multiple R&D projects simultaneously * Experience ...

Deep48

Production Operator

Terre Haute, IN · On-site

$18/hr

Deep48 is working with a global leader in the formulation, development and manufacture of performance polymer solutions to hire Production Operators for their Mobile Workforce Unit. This is an ...

Deep48

Production Operator

Terre Haute, IN · On-site

$18/hr

Deep48 is working with a global leader in the formulation, development and manufacture of performance polymer solutions to hire Production Operators for their Mobile Workforce Unit. This is an ...

Astrix Inc

R&D Manager

Columbus, IN · On-site

$90K - $100K/yr

Experience in product development or formulation. * Familiarity with regulatory and quality compliance standards. * Experience managing multiple projects simultaneously. *This is a complete list of ...

Astrix Inc

R&D Manager

Columbus, IN · On-site

$90K - $100K/yr

Experience in product development or formulation. * Familiarity with regulatory and quality compliance standards. * Experience managing multiple projects simultaneously. *This is a complete list of ...

Lancesoft

R&D Scientist

Terre Haute, IN · On-site

Follows and supports all Company Safety policies and procedures Responsible for the formulation and development of new products Re-engineer existing products Ensure that product aesthetics and other ...

Amrize

Principal Materials Scientist

Fishers, IN

This role bridges theoretical polymer physics and chemistry with practical formulation, ensuring rapid, data-driven product development from benchtop to commercialization. WHAT YOU'LL ACCOMPLISH ...

Amrize

Principal Materials Scientist

Fishers, IN · On-site

This role bridges theoretical polymer physics and chemistry with practical formulation, ensuring rapid, data-driven product development from benchtop to commercialization. WHAT YOU'LL ACCOMPLISH ...

Precision Color Compounds LLC

Be Seen First

Color Lab Technician

Fort Wayne, IN · On-site

$50K - $60K/yr

At least 3 years of experience in color matching and formulation in plastics (or equivalent ... development and quality assurance team.

Saturn Petcare Inc

R & D Scientist

Terre Haute, IN · On-site

As a part of the R&D team, the R&D scientist will develop strategies to improve existing products and processing, participate in the formulation and development of new products, participate actively ...

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Formulation Development information

What are some common challenges faced in a Formulation Development role, and how are they typically addressed?

Professionals in Formulation Development often encounter challenges such as ensuring product stability, achieving desired drug release profiles, and scaling up formulations from the laboratory to manufacturing. These challenges are typically addressed by conducting thorough pre-formulation studies, collaborating closely with analytical and process engineers, and performing iterative testing to optimize formulations. Teamwork and effective communication with quality assurance and regulatory teams are also crucial to ensure products meet both efficacy and compliance standards.

What are the key skills and qualifications needed to thrive in Formulation Development, and why are they important?

To excel in Formulation Development, a solid background in chemistry, pharmaceutical sciences, or related fields, often with a relevant degree, is essential. Experience with analytical instruments, formulation software, and knowledge of Good Manufacturing Practices (GMP) or regulatory guidelines are typically required. Strong problem-solving abilities, attention to detail, and effective cross-functional communication set top performers apart. These skills ensure the creation of safe, effective, and compliant products that meet both scientific and regulatory standards.

What is the difference between Formulation Development vs Formulation Scientist?

AspectFormulation DevelopmentFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fieldsBachelor's or Master's in Pharmacy, Chemistry, or related fields
Work EnvironmentResearch labs, pharmaceutical companies, R&D departmentsResearch labs, pharmaceutical companies, R&D departments
Industry UsageDesigning and optimizing drug formulations for productionDeveloping and testing drug formulations, conducting experiments

Formulation Development focuses on designing and optimizing drug formulations for manufacturing, while Formulation Scientists conduct experiments and testing to develop these formulations. Both roles require similar educational backgrounds and work environments, but their specific responsibilities differ in scope and focus.

What is formulation development?

Formulation development is the process of designing and optimizing the composition of a pharmaceutical product, such as a tablet, capsule, or injectable, to ensure its safety, efficacy, and stability. This involves selecting appropriate active ingredients, excipients, and delivery methods to achieve the desired therapeutic effect. Professionals in formulation development work to address challenges like solubility, bioavailability, and manufacturability, while ensuring compliance with regulatory standards. Their work is essential for turning a drug candidate into a viable, market-ready product.
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What cities in Indiana are hiring for Formulation Development jobs? Cities in Indiana with the most Formulation Development job openings:
Formulation Development jobs near you
Formulation & Prep Supervisor, 2nd shift

Formulation & Prep Supervisor, 2nd shift

INCOG BioPharma Services

Fishers, IN • On-site

$56K - $77K/yr

Full-time

Posted 15 days ago

Job description

Description
Manufacturing Supervisor Summary:
The Manufacturing Supervisor is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor support and review of MBR's, providing coaching and feedback to operations team. Involvement in manufacturing deviation investigations and CAPA implementation. Influencing the accomplishments of companywide and team goals and objectives as well as inspiring team members while consistently modeling ALP values in all interactions.
This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs) The Manufacturing Supervisor will constantly evaluate the internal processes and procedures and work to create a productive space while maintaining the highest possible quality standards.
This is a 2nd shift role, with typical hours from 2:30PM-11:30PM.
Essential Job Functions:
• Provide technical support, oversite and team leadership in manufacturing batch activities.
• Coordinate the development of individual team members with routine one on ones, training oversite and training opportunities.
• Develop and improve current processes to maintain and control the formulation and filling operations.
• Assure compliance with cGMP requirements (current good manufacturing practices)
• Perform GEMBA walks and checks for process improvements.
Job Requirements:
• Knowledge of process control, quality engineering, sampling requirements, statistical techniques, and process capability
• Familiarity with relevant quality and regulatory requirements and trends and cGMP's
• Strong communication skills and the ability to build relationships with colleagues across all levels of the organization, including business managers, operations leaders, and technical leaders.
• Knowledge of Aseptic techniques and processing
Additional Preferences:
• 4-5 years demonstrated working knowledge of aseptic manufacturing operations.
• 1-2 years in a people leadership role
Additional info about INCOG BioPharma Services:
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.
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