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Formulation Manager Jobs in Mount Dora, FL (NOW HIRING)

Quality Manager - Pharmacy

Orlando, FL · On-site

$85K - $110K/yr

Review and approve SOPs, controlled forms, policies, master formulation records, and quality ... Manage supplier qualification and quality oversight of APIs, excipients, sterile components ...

In conjunction with the RPM, the property manager will assist in the formulation of budgets for each upcoming calendar year. The property manager is responsible for staying within the established ...

... Formulation of the Initial Care Plan. * Review all medical data which can be provided to update a case management plan which will incorporate contact with providers, payers, with the patient and with ...

... Formulation of the Initial Care Plan. * Review all medical data which can be provided to update a case management plan which will incorporate contact with providers, payers, with the patient and with ...

Review codes, standards, research and apply critical formulation of facts to develop conclusions that assist clients resolve concerns and are defensible. * Maintain good project data management ...

Review codes, standards, research and apply critical formulation of facts to develop conclusions that assist clients resolve concerns and are defensible. * Maintain good project data management ...

Review codes, standards, research and apply critical formulation of facts to develop conclusions that assist clients resolve concerns and are defensible. * Maintain good project data management ...

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Formulation Manager information

See Mount Dora, FL salary details

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$20

$37

How much do formulation manager jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for formulation manager in Mount Dora, FL is $20.19, according to ZipRecruiter salary data. Most workers in this role earn between $16.15 and $20.19 per hour, depending on experience, location, and employer.

What is a formulation manager?

Formulation Managers are professionals responsible for overseeing the development and optimization of product formulations, particularly in industries like pharmaceuticals, cosmetics, food, and chemicals. They lead teams to design, test, and refine product mixtures to meet quality, safety, and regulatory standards. Their role often involves coordinating with research, production, and quality assurance departments to ensure that product formulations are effective, stable, and cost-efficient. Formulation Managers also stay updated on industry trends and regulatory changes to keep their company's products competitive. Effective communication, project management, and technical expertise are key skills for this role.

What are some common challenges faced by a formulation manager in coordinating cross-functional teams?

Formulation Managers often work closely with R&D, quality assurance, regulatory, and production teams to bring new products from concept to launch. A common challenge is ensuring clear communication and alignment across departments, especially when dealing with tight timelines or shifting project priorities. Balancing technical requirements, regulatory compliance, and manufacturing feasibility can also be demanding. Successful Formulation Managers are proactive in problem-solving and skilled at fostering strong collaboration to keep projects on track.

What are the key skills and qualifications needed to thrive as a formulation manager, and why are they important?

To thrive as a Formulation Manager, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by an advanced degree and experience in product formulation. Familiarity with laboratory equipment, formulation development software, and regulatory compliance systems is typically required. Strong leadership, problem-solving, and project management skills help you effectively lead teams and navigate complex product development cycles. These competencies are crucial for ensuring product quality, regulatory adherence, and timely delivery of innovative formulations.

What is the difference between Formulation Manager vs Formulation Scientist?

AspectFormulation ManagerFormulation Scientist
CredentialsBachelor's or Master's in Chemistry, Pharmacy, or related field; often requires experience in project managementBachelor's or Master's in Chemistry, Pharmacy, or related field; focus on research skills
Work EnvironmentOversees teams in R&D or manufacturing settings, manages projects, and coordinates formulation developmentConducts laboratory research, experiments, and formulation testing
Industry UsageCommonly used in pharmaceutical, cosmetics, and chemical industries for leadership rolesPrimarily used in research and development departments for formulation development

The Formulation Manager typically oversees formulation projects, manages teams, and ensures product development aligns with business goals. In contrast, the Formulation Scientist focuses on conducting experiments and developing formulations in the lab. Both roles require similar educational backgrounds but differ in responsibilities and scope within the formulation process.

Quality Manager - Pharmacy

W3Global Inc.

Orlando, FL • On-site

$85K - $110K/yr

Full-time

Re-posted 18 days ago


Job description

Position Summary

we are seeking an experienced Quality Manager to lead the quality program for its sterile and nonsterile 503A compounding operations.

The Quality Manager will be responsible for building, maintaining, and continuously improving our Quality Management System while providing independent oversight of production, documentation, testing, personnel qualification, equipment, facilities, suppliers, and product release activities.

This is a critical leadership position with direct access to the Pharmacist-in-Charge and the authority to stop operations, quarantine materials or preparations, initiate investigations, and escalate quality or patient-safety concerns.

Key Responsibilities

  • Lead and manage the Quality Assurance, Quality Control, and Document Control functions.

  • Develop, implement, and maintain the pharmacy's Quality Management System.

  • Ensure compliance with applicable requirements, including USP <795>, USP <797>, USP <800> when applicable, Florida Board of Pharmacy requirements, and relevant 503A compounding standards.

  • Oversee deviations, nonconformances, CAPAs, change controls, complaints, recalls, and internal audits.

  • Review and approve SOPs, controlled forms, policies, master formulation records, and quality documents.

  • Ensure compounding and batch records are complete, accurate, and properly reviewed before release.

  • Oversee quarantine, approval, rejection, and release controls for components and compounded preparations.

  • Review environmental monitoring, personnel monitoring, sterility, endotoxin, potency, and other laboratory results as applicable.

  • Coordinate investigations related to environmental excursions, testing failures, documentation errors, and process deviations.

  • Oversee training, qualification, and competency records for pharmacy personnel.

  • Create Primary and secondary equipment qualification protocols.

  • Provide quality oversight for equipment qualification, calibration, certification, preventive maintenance, and validation activities.

  • Manage supplier qualification and quality oversight of APIs, excipients, sterile components, packaging, laboratories, and service providers.

  • Maintain inspection readiness and serve as the primary quality contact during regulatory inspections and client audits.

  • Present quality metrics, trends, risks, and corrective-action status to the PIC and company leadership.

Supervisory Responsibilities

The Quality Manager is authorized to:

  • Stop compounding, testing, dispensing, or related operations when a quality or patient- safety risk exists.

  • Quarantine materials, equipment, rooms, records, or compounded preparations.

  • Initiate deviations, investigations, CAPAs, change controls, supplier corrective actions, and recalls.

  • Reject incomplete or noncompliant documentation.

  • Require retraining or requalification of personnel.

  • Recommend approval or rejection of materials and compounded preparations.

  • Escalate unresolved quality concerns directly to the PIC and ownership.

Required Qualifications

  • Minimum of five years of experience in compounding pharmacy, pharmaceutical manufacturing, quality assurance, laboratory quality, or another regulated healthcare or life-sciences environment.

  • Minimum of two years of quality leadership or supervisory experience.

  • Experience with deviations, CAPA, change control, document control, internal audits, training systems, supplier qualification, and record review.

  • Working knowledge of USP <795>, USP <800> and USP <797>.

  • Strong technical writing, investigation, organizational, and analytical skills.

  • Ability to make independent quality decisions and challenge production when necessary.

Preferred Qualifications

  • Experience in a 503A or 503B compounding pharmacy.

  • Experience with both sterile and nonsterile compounding.

  • Experience with USP <797> Category 3 operations.

  • Experience with environmental monitoring, sterility testing, endotoxin testing, stability programs, and laboratory investigations.

  • Experience preparing for Board of Pharmacy, FDA, accreditation, or client inspections.


W3Global logo

About W3Global

Sourced by ZipRecruiter

W3Global has been delivering staffing solutions for nearly two decades; we know which recruiting strategies work best. Our expert team is committed to developing a customized solution to fit your company’s unique needs. As a W3Global client, you’ll also receive personalized assistance from a seasoned team of staffing specialists. We are committed to providing both technical support and industry expertise to simplify the hiring process. We know that your time matters. W3Global will help you streamline the hiring process, getting it done and getting it right.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Frisco, TX, US

Year founded

2006