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Regeneron

Director, Biotech Production

Regeneron

Director of Biotech Production leading manufacturing readiness for a new biologics drug facility. Collaborating with teams to ensure operational standards are met in Saratoga Springs, New York.

Posted 7/15/2026full-timeSaratoga Springs • New York • 🇺🇸 United StatesLead💰 $172,200 - $286,900 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading operational start-up and management of biologics manufacturing facilities, ensuring compliance with GMP standards while fostering a high-performing team. Proficient in translating corporate objectives into actionable strategies and maintaining operational efficiency through effective collaboration across departments.

Highest-signal resume keywords
Biopharmaceutical ManufacturingGMP ComplianceOperational Start-Up LeadershipSCADA, DCS, MES, and PAT TechnologiesTeam Development and Performance Management

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Biologics ManufacturingRecombinant Protein ProductionValidation ActivitiesEquipment CommissioningMetrics Tracking and Trending
Soft Skills
Ownership and AccountabilityCollaborationAdaptability
Tools & Technologies
SCADADCSMESPAT TechnologiesIndustry 4.0 Technologies
Industry Keywords
BiopharmaceuticalBiotechGMP Production FacilityClinical ManufacturingCommercial Manufacturing

About the role

Key responsibilities & impact
  • Leads the manufacturing team through facility start-up, setting the operating standards for a brand-new biologics plant
  • Directs manufacturing of recombinant proteins according to approved protocols, regulations, and schedules across 2,000L and 10,000L bioreactor suites
  • Translates corporate objectives into strategy, connecting floor-level performance to global IOPS goals
  • Guides validation activities and equipment commissioning/qualification to ensure operational readiness
  • Partners across Facilities, Process Development, Quality, and Regulatory to keep production running smoothly
  • Builds and develops a high-performing team, embracing the ambiguity that comes with standing up a new site
  • Tracks and trends key metrics to keep operations safe, compliant, and efficient
  • Thrives on ownership, taking accountability for team performance and results from day one

Requirements

What you’ll need
  • Bachelor's in a physical or biological science or chemical engineering
  • 12+ years of biopharmaceutical/biotech work in a GMP production facility
  • 8-10 years (MA/MS), or 4-7 years (PhD) of biopharmaceutical/biotech work in a GMP production facility
  • Demonstrated experience leading operational start-up for a clinical and commercial biologics manufacturing facility
  • Experience working with industrial systems such as SCADA, DCS, MES, and PAT technologies
  • Familiarity with other Industry 4.0 technologies and strategies is a plus
  • Regular presence on the production floor and entry into classified/controlled environments requiring gowning

Benefits

Comp & perks
  • annual bonuses or other incentive plans
  • equity awards
  • pension or retirement benefits
  • 401(k) company match
  • health and wellness programs
  • fitness centers
  • insurance benefits (e.g. medical, dental, vision, life and disability)
  • paid time off
  • family support benefits