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Director of Contract Manufacturing, Supplements
JuneShineDirector of Contract Manufacturing overseeing external manufacturing functions for supplements at JuneShine Brands. Responsible for production schedule, quality compliance, and partner management.
Posted 5/7/2026full-timeSan Diego • California • 🇺🇸 United StatesLead💰 $150,000 - $170,000 per yearWebsite
Tech Stack
Tools & technologiesERPOracle
About the role
Key responsibilities & impact- Own and develop a portfolio of supplement co-manufacturing partners - from identification, evaluation, and onboarding through ongoing performance management, SLAs, and contract negotiation
- Serve as JuneShine Brand's primary relationship owner with all supplement manufacturers; conduct regular site visits, capability assessments, and cGMP audits to drive continuous improvement and hold partners to standard
- Directly manage and develop the External Quality Manager, Supplements
- Translate demand forecasts into detailed, executable production schedules across the co-manufacturing network; own on-time delivery to our distribution commitments
- Partner with Supply Chain to align raw material and packaging supply at co-manufacturers, manage inventory levels to optimize working capital, and resolve production bottlenecks and non-conformances in real time
- Ensure all supplement products meet FDA, cGMP, NSF, and internal quality standards; drive CAPA resolution with manufacturing partners and ensure certifications and documentation stay current
- Own COGS targets, tolling costs, and budget performance; lead cost reduction and efficiency initiatives across the network without compromising quality or delivery; establish KPIs and report regularly to the VP of Product on network health, risks, and opportunities
- Support label accuracy and product specification integrity across all externally manufactured supplement SKUs
- Partner with R&D on new product development - co-manufacturer selection, trial runs, scale-up, and full commercial launch readiness across new supplement formats and SKUs
- Collaborate with Marketing, Sales, and Product to align on timelines, specs, and launch priorities; lead co-manufacturer onboarding projects from contract execution through first commercial production
Requirements
What you’ll need- 21 years of age or older at the time of application
- 6-8+ years of experience in contract or co-manufacturing management within dietary supplements, nutraceuticals, or functional health and wellness
- Demonstrated expertise across multiple supplement dosage forms: powders, gummies, stikpaks, and nutraceuticals
- Strong working knowledge of FDA 21 CFR Part 111, cGMP, NSF, and USP compliance requirements for dietary supplements
- Proven track record managing R&D scale-up, formula transfer, and new product commercialization at contract manufacturers
- Proficiency in ERP systems (NetSuite, SAP, or Oracle) for production planning and operational reporting
- Hands-on experience managing COGS, tolling costs, and gross margin performance
- Ability and willingness to travel 25–35% to co-manufacturing facilities
Benefits
Comp & perks- Unlimited Paid Time Off
- Healthcare coverage: up to 90% company contribution for employees and 25% for dependents
- Voluntary vision, dental, and accidental plans
- 401(k) with up to 4% company match
- 12 weeks of paid Equal Parental Leave, $500 Baby Bonding Bucks, and a sustainable baby gift
- Booch, spirit, beer, and soft good perks
- And more!
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
contract managementco-manufacturing managementproduction schedulingcost reductioninventory managementCAPA resolutionnew product commercializationR&D scale-upformula transferquality management
Soft Skills
relationship managementleadershipcollaborationcommunicationproblem-solvingorganizational skillsperformance managementanalytical skillsnegotiationproject management