Sr. Product Quality Specialist

Bora PharmaceuticalsMaple Grove, MN
$88,000 - $125,000Onsite

About The Position

The Senior Product Quality Specialist is a senior-level quality professional responsible for providing independent quality oversight of manufacturing operations and execution of quality systems. This role serves as a primary quality representative for assigned clients and project teams, leading complex quality activities including review of complex and high-risk documentation, reviewing and supporting critical investigations, supporting audits, and approving Annual Product Reviews (APRs). The Senior Specialist acts as a subject matter expert within QA Operations, ensuring compliance with cGMP requirements, company procedures, and client/regulatory expectations while supporting continuous improvement initiatives and maintaining strong client relationships.

Requirements

  • Bachelor’s degree
  • 6 years of direct work experience required in a pharmaceutical/biotechnology operations or other GMP-related industry with a minimum of 2 years of experience in Quality Assurance or Quality Control.
  • Strong knowledge of cGMP regulations and pharmaceutical quality systems.
  • Strong technical writing and documentation review skills.
  • Excellent analytical, problem-solving, and decision-making abilities.
  • Ability to work independently with minimal supervision.
  • Strong verbal and written communication skills.
  • Ability to effectively manage multiple priorities in a fast-paced manufacturing environment.
  • Strong computer skills required.
  • Knowledge of the following software packages is strongly recommended: SAP, Veeva, Microsoft Suite (including Word, Excel, Visio, and PowerPoint).
  • Demonstrated experience reviewing and approving complex GMP documentation.
  • Broad knowledge of quality systems and experience leading investigations and performing quality risk assessments.
  • Experience supporting client, regulatory, and internal audits.

Nice To Haves

  • ASQ certification such as CQIA, CQA, or CQE

Responsibilities

  • Review and approve complex and major-risk GMP documents, including SOPs, validation protocols/reports, change controls, and technical reports.
  • Author, support, review and approve major-risk investigations, including deviations, CAPAs, complaints, laboratory investigations, and effectiveness evaluations to ensure quality, compliance, and appropriate root cause determination.
  • Conduct risk assessments and recommend appropriate corrective and preventive actions.
  • Evaluate quality events and documentation for regulatory compliance, product quality impact, and patient safety considerations.
  • Independently represent Quality Assurance on cross-functional project teams and provide quality leadership for assigned products and programs.
  • Serve as the primary Quality contact for assigned clients and maintain strong client relationships.
  • Provide quality guidance and risk-based decision-making support to Manufacturing, Quality Control, Engineering, Validation, and other functional groups.
  • Support internal, customer, and regulatory audits by serving as a Quality subject matter expert and audit scribe.
  • Review and approve Annual Product Reviews (APRs) and assess quality trends, product performance, and process capability.
  • Provide Quality oversight for material/equipment activations and other SAP product related activities, ensuring compliance with applicable procedures and regulatory requirements.
  • Support continuous improvement initiatives that strengthen quality systems, operational efficiency, and regulatory compliance.
  • Mentor and provide technical guidance to junior-level QA personnel.
  • Ensure compliance with applicable cGMP regulations, company procedures, and client quality requirements.
  • Function as a subject matter expert within QA Operations by independently making quality decisions within established procedures and quality systems and influencing quality outcomes through collaboration and expertise.
  • Ability to effectively manage multiple priorities in a fast-paced manufacturing environment.
  • Perform junior QA tasks, including batch record review, document control, and other responsibilities as assigned to support business operations.

Benefits

  • Competitive salary and performance-based incentives
  • Comprehensive health coverage including medical, dental, and vision insurance
  • Retirement savings plans with employer matching contributions
  • Paid time off
  • Professional development opportunities
  • Employee wellness programs and resources
  • Employee Assistance Program and Mental Health Resources
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service