CCI Technology Lead

Ddltesting; Eden Prairie (MN); On-site; USD 120,000 - 140,000; Full time

Benefits offered by this job

Medical Insurance

Vision Insurance

Health Savings Account (HSA)

Flexible Spending Account (FSA)

Basic Life and AD&D / Voluntary Life

Short-Term Disability

Long-Term Disability

Pet Insurance

401(k) Retirement Plan

Paid Holidays

PTO

Job summary

DDL, Inc. is seeking a CCI Technology Lead in Eden Prairie, MN. This full-time role leads CCIT laboratory operations, oversees method development and validation, and ensures compliance with USP <1207>, cGMP, and ISO 17025. The position includes directing staff, audits, and collaboration with clients.

Salary ranges from $120,000 to $140,000 annually with bonus eligibility up to 10%. Occasional travel up to 20% may be required. Strong technical writing and leadership are essential.

Qualifications

• Bachelor’s or Master’s degree in Engineering, Chemistry, Materials Science, or related field.
• 7+ years of experience in pharmaceutical, medical device, or regulated laboratory environment.
• Direct experience with CCIT methods and USP <1207> required.
• Experience in CDMO or contract testing laboratory environment required.
• Knowledge and understanding of CCIT instrumentation operation and test execution.
• Demonstrated leadership experience managing technical teams.
• ISO 17025 laboratory experience and familiarity with cGMP

Responsibilities

• Establish, lead, and manage CCIT laboratory operations in a regulated environment.
• Serve as technical SME for USP <1207> and related regulatory requirements.
• Oversee method development, validation, and routine testing activities.
• Lead audits for FDA and client inspections and support CAPA programs.
• Review protocols, reports, deviations, and validation summaries.
• Drive continuous improvement of quality, efficiency, and lab performance.
• Collaborate with Business Development on proposals and scope.
• Train, mentor, and develop technical staff.

Skills

CCIT methods

Leadership

Regulatory compliance

Laboratory operations

Technical writing

Client facing

Education

Bachelor's or Master's in Engineering, Chemistry, Materials Science

Tools

Microsoft Office

LIMS

QMS System

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

CCI Technology Lead

Full‑Time Professional DDL - Minnesota, Eden Prairie, MN, US

Salary Range: $120,000.00 To $140,000.00 Annually

WHO WE ARE

DDL, Inc. is a third‑party testing facility dedicated to helping medical device and pharmaceutical companies across the globe bring products to market. For over 30 years, DDL has provided extraordinary customer service and specialized testing expertise to the medical device, pharmaceutical, and consumer goods industries for our clients’ safety and efficacy testing. We help save lives by providing the highest standards for package, product and material, and Container Closure Integrity testing.

COMPENSATION

This position has a starting base salary range of $120,000–$140,000 and includes eligibility to earn an annual bonus of up to 10% of base salary.

HOW YOU WILL CONTRIBUTE (Overview & Key Responsibilities)

The CCIT Technical Lead is responsible for establishing, leading, and managing Container Closure Integrity Testing (CCIT) laboratory operations in a regulated environment. This role serves as the technical subject matter expert for USP <1207> and related regulatory requirements, while overseeing method development, validation, and routine testing activities. The position combines technical leadership, operational management, and client‑facing responsibilities to support high‑quality, compliant laboratory services.

• Develop and implement CCI strategies aligned with USP <1207>, FDA guidance, and industry best practices
• Lead and manage day‑to‑day CCI laboratory operations, including staffing, scheduling, and workflow optimization
• Design and develop CCI methods including vacuum decay, high voltage leak detection (HVLD), helium leak detection, and headspace analysis – Define method parameters, detection limits, and acceptance criteria based on package configuration and risk assessment
• Lead internal and external audits for CCI, including FDA and client inspections
• Review, support and approve protocols, reports, deviations, and CAPA investigations
• Drive continuous improvement initiatives related to quality, efficiency, and lab performance
• Collaborate with Business Development to support client proposals, project scoping and technical discussions
• Execute and document method development, feasibility studies, and protocol‑driven testing
• Lead and support method validation activities and method transfer projects
• Interpret test results, perform statistical analysis, and provide technical conclusions
• Author and review technical documentation including protocols, reports, SOPs, and validation summaries as it relates to CCI
• Collaborate with QA and regulatory teams to ensure compliance with cGMP, ISO 17025, and USP <1207>
• Identify opportunities and develop CCI studies for publication.
• Build and maintain relationships with key technical leaders and customer stakeholders in CCI analysis.
• Proactively develop knowledge of industry & technology as it applies to the area of CCI Analysis to effectively support organization in identifying and growing future analytical expertise
• Work proactively with the Commercial team to understand the voice of customer and put together a plan to bring the necessary capability and technology into the DDL organization to support our business
• Train, mentor, and develop technical staff including scientists, engineers, and technicians

WHAT YOU NEED TO SUCCEED (Minimum Qualifications)

• Bachelor’s or Master’s degree in Engineering, Chemistry, Materials Science, or related field
• 7+ years of experience in pharmaceutical, medical device, or regulated laboratory environment
• Direct experience with CCIT methods and USP <1207> required
• Experience in CDMO or contract testing laboratory environment required
• Knowledge and understanding of CCIT instrumentation operation and test execution
• Demonstrated leadership experience managing technical teams
• Other Skills Required (computer, language, etc.): Microsoft Office, LIMS, QMS System
• Ability to travel up to 20%
• Strong knowledge of cGMP, FDA regulations, and quality systems
• Experience leading validation programs and regulatory audits
• Strong technical writing and documentation skills
• Familiarity with deterministic leak detection technologies
• ISO 17025 laboratory experience
• Six Sigma or Lean certification
• Client‑facing or consulting experience
• Experience participating in industry working groups

WHY JOIN US

If you’re a team player who is looking for a sense of accomplishment, the opportunity to grow both personally and professionally, and a place to call home, then DDL is the place for you! At DDL, Inc., we strive to offer a competitive salary along with a comprehensive benefits package that helps you and your family maintain health and well‑being – both physically and financially. Our comprehensive benefits package includes:

• Medical Insurance
• Vision Insurance
• Health Savings Account (HSA)
• Flexible Spending Account (FSA) – Voluntary Accident, Critical Illness, and Hospital Indemnity Insurance
• Basic Life and AD&D / Voluntary Life and AD&D
• Short‑Term Disability
• Long‑Term Disability
• Pet Insurance
• 401(k) Retirement Plan with Safe Harbor Employer Contribution
• Paid Holidays
• PTO

It is DDL’s policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.