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CAI

Operational readiness consulting for pharma

Senior Quality, Compliance, and Regulatory Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBoston, MA, USA$130k - $175k /yrHybrid

About the Job

Requirements

  • A BS or higher in Biotechnology, Chemistry, Pharmaceutical Manufacturing Technology, Industrial Pharmaceutical Science, Pharmaceutical Technology and Quality Systems, Engineering, or a related scientific discipline.
  • At least 8 years of experience in the life sciences industry, with a proven track record of leading or collaborating effectively within cross-functional teams.
  • In-depth knowledge of current Good Manufacturing Practice (cGMP) systems, Quality Assurance, regulatory affairs, pharmaceutical manufacturing, and testing, with direct experience in manufacturing environments.
  • Technical leadership experience in developing and implementing a Quality Management System (QMS).
  • Knowledge of local and international data regulations, ensuring integrity, security, and compliance.
  • Skill in cGMP environments, covering quality manufacturing, production practices, and systems.

Responsibilities

  • Work collaboratively with CAI agents to sell Quality, Compliance, and Regulatory services and deliver strategic project work.
  • Leverage a professional network to attract new business opportunities, generate leads, and secure assignments for consultants through proactive and targeted sales efforts.
  • Engage in industry forums by speaking, writing articles, participating in professional society committees, and supporting standards or guidance document creation within such groups.
  • Build and maintain relationships with regulatory authorities and other stakeholders to support access and influence.
  • Consult clients in Quality, Regulatory, and Compliance areas.
  • Fulfill Quality, Regulatory, and Compliance roles while managing client relationships for a portfolio of products and liaising closely with management and other key personnel in accordance with project schedules.
  • Engage in strategic project work designed to open opportunities for larger teams after an initial expert engagement, or deliver specialized expertise as part of a larger project.
  • Create and contribute content on industry-changing approaches for CAI's website and marketing materials.
  • Support the Practice Area Lead with quality systems, knowledge management, service definition, and delivery within the area of expertise.
  • Develop and grow agents through tailored professional development plans and initiatives.
  • Lead and mentor teams, influencing peers and stakeholders to achieve results.
  • Write technical documents and present business ideas.
  • Make timely, informed decisions by gathering relevant information, asking questions, and working with peers to identify solutions.
  • Identify improvement opportunities and simplify processes.
  • Resolve issues, plan independently, seek feedback, take action, and promote continuous improvement.
  • Maintain relationships at all levels, share knowledge, and communicate constructively.

Desired Qualifications

  • Prior experience in sterile manufacturing, biotechnology, medical devices, and/or cell and gene therapy is highly advantageous.

About the Company

CAI

Operational readiness consulting for pharma

CAI Technical Consulting Malaysia SDN (brand cagents.com) provides operational readiness consulting for pharmaceutical, biotech, and healthcare firms. It helps clients prepare for full-scale production through quick operational readiness assessments, gap-tailored plans, and hands-on implementation support in areas like project planning, production operations, asset management, reliability, and sustainability, plus Digital Pathology Validation for Leica Biosystems to meet regulatory standards. The firm differentiates itself by combining rapid assessments with practical, cost-effective strategies, ongoing industry collaboration, and global delivery that informs tailored solutions. Its goal is to help clients accelerate their path to compliant, scalable operations and successful production scale-up.

Company size
1,001-5,000
Company stage
Pre-seed
Total funding
$3.4M
Headquarters
Indianapolis, IN
Founded
1996

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