Full-Time

Customer Quality Lead

Quality Assurance

Updated on 9/3/2026

Curia

Curia

1,001-5,000 employees

End-to-end drug development and manufacturing

Compensation Overview

$117k - $146.5k/yr

+ 401(k) matching contributions + Relocation assistance

Rensselaer, NY, USA

In Person

Relocation assistance is offered.

Bachelor's

Category
Manufacturing Quality & Test (1)
Required Skills
FDA Regulations
Quality Assurance (QA)
Customer Service

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Requirements
  • A minimum Bachelor of Science degree in Biology or a related scientific field.
  • A minimum of 10-15 years of experience in quality assurance, active pharmaceutical ingredient process development, technical services, or good manufacturing practice compliance in the pharmaceutical industry at United States Food and Drug Administration-regulated facilities.
  • Working experience managing global customers and global cross-functional teams.
  • Broad knowledge of current good manufacturing practices, Food and Drug Administration regulations, and international regulations, including 21 CFR Parts 11, 210, 211, and 820, European Union good manufacturing practice, and ICH Q7.
  • Knowledge of pharmaceutical manufacturing operations.
  • Experience with United States Food and Drug Administration inspections, such as participating in or interacting with investigators.
  • Ability to work cross-functionally across internal stakeholders, with communication, organizational, negotiation, influencing, and collaboration skills.
  • Proficiency in building consensus, negotiating, escalating issues, and providing customer service.
  • Understanding of the importance and use of quality metrics.
  • Must pass a background check and drug screen.
  • May be required to pass occupational health screening.
Responsibilities
  • Demonstrate exemplary customer quality service to internal and external customers while reporting to the site Quality Head.
  • Write and review customer product investigations, coordinate with Quality Assurance on customer comments related to batch records, and ensure timely disposition of product lots.
  • Coordinate and prepare temporary or planned change controls associated with customer products.
  • Ensure on-time completion of customer and regulatory commitments specific to customer projects.
  • Ensure timely completion of annual product reviews and assessment of continued process verification and validation activities.
  • Serve as the primary point of contact for customer-related queries from Sales and Business Development.
  • Build relationships with Quality Control, Quality Assurance, Regulatory Affairs, and other stakeholders to obtain and assess data for customer requests and inquiries.
  • Coordinate and assist with customer requests supporting customer filings and amendments, and liaise with Regulatory Affairs and site stakeholders to ensure reviews meet quality agreement requirements.
  • Monitor agreed-upon tasks, escalate issues and delays to the site Quality Head, and prepare contingency plans with internal partners.
  • Review and approve customer complaint investigations, assess root cause analyses, implement corrective and preventive actions, and review their effectiveness.
  • Lead initiatives to improve and harmonize quality processes and customer satisfaction.
  • Support stakeholders in the new product introduction process for Quality Control and Quality Assurance activities.
  • Build and maintain knowledge of the site pipeline to understand customer requests.
  • Participate in customer meetings and support product development as needed.
  • Ensure quality assurance agreements are reviewed and approved in a timely manner and maintain current effective versions.
  • Coordinate with the site Compliance team to schedule and support customer audits.
  • Lead good manufacturing practice activities associated with customer products and work with managers and supervisors to complete deviation investigations on time.
  • Participate in the site Quality Management Review, provide data, and execute improvement plans.
  • Oversee customer-specific corrective and preventive actions, monitor completion, and provide updates to customers and management.
  • Interact with the Curia Quality network to share information about quality expectations, inspections, audits, and quality-system harmonization.
  • Assist QA leadership in mentoring and coaching QA Specialists when requested.

Curia is a contract development and manufacturing organization (CDMO) that partners with pharmaceutical and biotech companies to move medical breakthroughs from concept to market. It provides end-to-end services across the drug development lifecycle, including early research, method development and validation, preformulation, material science, solid-state chemistry, and package device testing. Revenue comes from service contracts for specialized capabilities and expertise, with clients ranging from small startups to large pharma. Curia also collaborates with industry leaders to advance continuous flow development and manufacturing programs. The company differentiates itself through flexible and scalable solutions, deep scientific expertise, and state-of-the-art technology that help clients accelerate development timelines while navigating discovery to commercialization. Its goal is to enable efficient, reliable progression of drug candidates from conception through to market approval.

Company Size

1,001-5,000

Company Stage

Debt Financing

Total Funding

$132M

Headquarters

Albany, New York

Founded

1991

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Simplify Jobs

Simplify's Take

What believers are saying

  • Curia expanded Glasgow sterile drug product capacity in March 2026.
  • Curia completed a $4 million sterile API upgrade in Valladolid in October 2025.
  • Curia won a 2025 CDMO Leadership Award in Global Biologics.

What critics are saying

  • Curia is closing Burlington in 2026 and cutting 81 jobs.
  • Curia is working on an out-of-court restructuring with private credit lenders.
  • Asset sales like Pace’s New Jersey lab purchase signal continued portfolio shrinkage.

What makes Curia unique

  • Curia spans discovery through commercial manufacturing across small molecules and biologics.
  • Curia manufactures mRNA and self-replicating RNA, including Replicate Bioscience’s RBI-4000.
  • Curia runs 20+ global sites with sterile fill-finish and cell-line development.

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Benefits

Paid Vacation

401(k) Retirement Plan

401(k) Company Match

Tuition Reimbursement

Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
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