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Research And Development Manager

Job in Tampa, Hillsborough County, Florida, 33646, USA
Listing for: PMAD
Full Time position
Listed on 2026-07-14
Job specializations:
  • Research/Development
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below

The R&D Manager is responsible for leading PMAD's research and development function, including formulation, sample development, product improvement, customer feasibility review, commercialization readiness, and R&D to-production transfer for PMAD's private‑label and white‑label CPG manufacturing business. This is a hands‑on technical leadership role for a small but highly visible R&D function. The R&D Manager converts customer concepts, sales priorities, production realities, ingredient availability, quality requirements, and PMAD's manufacturing capabilities into documented, scalable, compliant, and commercially viable products.

The role may supervise R&D Associates or other assigned R&D personnel as the department grows.

Essential Duties and Responsibilities
  • Manage PMAD's R&D pipeline, including product‑development requests, sample priorities, formula revisions, troubleshooting needs, internal innovation, and commercialization projects.
  • Translate customer concepts and business priorities into practical R&D plans, timelines, sample requirements, resource needs, and decision points.
  • Maintain visibility into R&D priorities, project status, customer‑development risks, resource constraints, formula‑change risks, and commercialization timelines.
  • Coordinate R&D priorities with Sales, Customer Success, QA/QC, Procurement, Production, Packaging, Warehouse, Finance, and Operations leadership.
  • Build repeatable R&D routines that reduce reliance on memory, informal formula notes, uncontrolled spreadsheets, or single‑person knowledge.
  • Support department growth by helping define role clarity, training needs, tools, trackers, SOP needs, and scalable R&D workflows. Formulation, Sample Development, and Product Improvement
  • Lead formulation and product‑development work across applicable PMAD product formats, including gummies, center‑fill products, blister products, liquid fills, powders, chocolates, and other PMAD‑supported product lines.
  • Develop, improve, and document recipes, formulas, ingredients, process steps, target specifications, sensory attributes, process notes, and sample records.
  • Oversee prototype development, bench samples, trial batches, pilot work, reformulations, ingredient substitutions, and flavor, texture, color, appearance, and performance adjustments.
  • Evaluate ingredient functionality, active load, process stability, customer requirements, manufacturability, sensory feedback, and packaging fit during product development.
  • Ensure sample work is clearly labeled, traceable, controlled, protected, and prepared according to approved R&D instructions and PMAD quality expectations.
  • Protect confidential customer formulas, prototypes, samples, specifications, product concepts, development records, and proprietary information.
Commercialization and Production Transfer
  • Lead the movement of products from concept to sample, sample to approved formula, approved formula to production‑ready documentation, and production‑ready documentation to commercial manufacturing.
  • Partner with QA/QC to confirm specification readiness, testing needs, release criteria, label considerations, documentation controls, customer approvals, and quality approval requirements before commercial use.
  • Partner with Production and Packaging to confirm that formulas and processes can be manufactured at scale using PMAD's equipment, staffing, batch sizes, sanitation practices, environmental controls, and packaging formats.
  • Prepare or support R&D‑to‑production transfer materials, including approved formulas, process parameters, ingredient and packaging requirements, quality checks, yield expectations, labor assumptions, sanitation considerations, and training needs.
  • Support trial batching, pilot runs, scale‑up batches, first production runs, and production troubleshooting that may require formulation, ingredient, process, equipment, or packaging adjustments.
  • Escalate manufacturability, quality, cost, timeline, equipment, material, or customer‑approval risks before PMAD commits to pricing, samples, or production deadlines.
cGMP, SOP, QA/QC, and Documentation Controls
  • Ensure R&D activities follow approved SOPs, cGMP expectations, sanitation requirements,…
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