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Senior Product Quality Manager; Peptide Technology

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Allergan
Full Time position
Listed on 2026-06-07
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist, QA Specialist / Manager, Quality Control / Manager
Salary/Wage Range or Industry Benchmark: 100000 - 130000 USD Yearly USD 100000.00 130000.00 YEAR
Job Description & How to Apply Below
Position: Senior Product Quality Manager (Peptide Technology)

Job Description

Responsible for quality of assigned new product introduction programs to ensure business objectives are met with regards to on‑time deliverables of program development while assuring compliance with local, divisional, and corporate policies and external agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), and Drug Products produced by Abb Vie plants or by third‑party manufacturers, in licensing relationships, or co‑marketing relationships.

Develop in concert with the appropriate regulatory strategies set forth by the governance processes.

Abb Vie Operations Quality Assurance is seeking a Product Quality Manager to lead quality deliverables for late‑stage development and commercialization of peptides, from registration through commercialization. We are seeking a highly motivated candidate with a proven track record of accomplishment in the field of peptide manufacturing development, to work in a multi‑functional team environment at our North Chicago, IL location.

  • Leads the development and implementation of global Product Quality Assurance strategy to support New Product Introduction (NPI) programs for the end‑to‑end commercial supply chain both at Abb Vie plants as well as contract manufacturing facilities. Drives implementation of the Product Transfer Process. Primary driver for product quality risk management and compliance aspects of product development.
  • Acts as global quality lead to support regulatory submission by developing, reviewing and approving relevant module 3 documents. Works with Regulatory Affairs and coordinates with GMP manufacturing sites to prepare submissions and provides responses to agency submission deficiencies/questions in a timely manner. Leads and manages pre‑approval inspection readiness for the NPI programs. Ensures regulatory approvals are obtained with no delays to market entries.
  • Leads the selection of external manufacturing partners from Quality for NPI programs. Leads the quality partner assessment and upskilling of the partners to meet Abb Vie Operations’ expectations. Partners with Quality Assurance audit team to qualify external manufacturing partners.
  • Communicates and negotiates with external manufacturing partner quality organization to maintain a consistent level of quality. Provides quality oversight to maintain partner qualification for development and commercialization.
  • Supports the management of exception documents and Corrective and Preventive Actions. Coordinates input from technical groups to determine root cause and implement appropriate actions. Serves as global quality representative at the change review board to drive/support global change plans needed for NPI programs.
  • Establishes and maintains relationships and open communication with cross‑functional groups to maintain roles and responsibilities and provides guidance on quality concerns. Drives continuous improvement for NPI programs.
Qualifications
  • Bachelor’s Degree in relevant science field required. Total combined years of experience:
    Minimum 8+ years. At least 3 years in Quality Assurance Operations Management; 5+ years in any of the following areas:
    Operations, Research and Development, Regulatory. Direct manufacturing plant experience in a pharmaceutical setting is preferred.
  • Comprehensive understanding of pharmaceutical technologies, specifically peptide technology is required. Experience in pharmaceutical development and commercialization is preferred.
  • Strong quality assurance/control background is required. Experience with FDA and other regulatory agency interactions and inspections is required.
  • Interacts well with diverse groups within function and maintains strong working relationships with internal and external collaborators.
Additional Information
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less…
Position Requirements
10+ Years work experience
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