ICQ Careers

What Can We Build Together?

Friendly business meeting with clients

Long-Lasting Client Relationships

When it comes to clients, we build relationships, not transaction. We see ourselves as part of our clients’ internal teams, and sometimes they think we really are!

Female Worker Wearing Protective Clothing in Pharmaceutical Plant

A Rewarding Career

Learn from ICQ’s industry-leading CQV experts with senior-level support and mentorship throughout your career. We never stop learning from each other, and we’re invested in your success. The more you grow professionally, the more our clients benefit.

Four healthcare workers in scrubs walking in corridor

Close Friendships

When you’re surrounded by like-minded, hardworking, dedicated professionals, you’re bound to become more than coworkers. We respect each other professionally just as much as we like one another personally.

Current Openings

Job Summary

The candidate will be a part of the ICQ Consultants team and will be responsible for the development and execution of protocols and final summary reports for Commissioning (IV/OV), Qualification (IQ/OQ/PQ) activities with a focus on processes, equipment and utilities.

Required Skills

  • 2 to 6 years of Commissioning, Qualification and/or Validation (CQV) with experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device industry.
  • Experience writing protocols, performing execution for processes, equipment and utilities used in the Biotech or Pharmaceutical Industry.
  • Direct experience within the following areas; Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Commissioning, Installation, Operational and/or Performance Qualification (IQ, OQ and PQ) protocols, Standard Operating Procedure (SOP), Change Control, Data Analysis, Deviations, Master Validation Plans, Risk Assessments, CAPAs, GMP investigations, Quality Risk Management (QRM), single use technologies.

Responsibilities

  • Successfully working within a multi-disciplinary team coordinating and delivering project activities meeting schedule, budgetary and quality expectations of the client.
  • Customarily and regularly exercises discretionary and independent judgment in performing the job.
  • Participate in training to ensure continued accreditation.
  • Maintain a safe working environment for self, team members and client staff.
  • Other tasks in alignment with your skills and competencies as required by the project, client and/or management.

Essential Qualities

  • Excellent organizational, verbal, and written communication skills; with demonstrated ability to efficiently and effectively, communicate with cross-functional teams and management on recommended course of action, with minimal assistance.
  • Proficient computer skills and be experienced using MS Office software (Word, Excel, and PowerPoint) and MS Project (as needed).
  • A self-starter, detail oriented and able to work independently with minimal supervision.
  • Excellent troubleshooting skills: ability to react quickly to understand and solve problems.

Education & Experience Requirements

B.S. degree in Biology, Biochemistry, Chemistry, Engineering, or equivalent years’ experience working in FDA-regulated industries.

Please note that only local candidates will be considered.

Job Summary

The candidate will be a part of the ICQ Consultants team and will be responsible for the development and execution of protocols and final summary reports for Computer System Validation (CSV) activities.

Required Skills

  • 2 to 6 years of Computer System Validation with additional CQV experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device industry.
  • Experience writing protocols, performing execution for processes, equipment and utilities used in the Biotech or Pharmaceutical Industry.
  • Direct experience within the following areas; Computer System Validation (CSV), Data Integrity, 21CFR Part 11, ERES, Enterprise Systems Qualification, Master Validation Plans, Standard Operating Procedure (SOP), Change Control, Data Analysis, Deviations, Risk Assessments, CAPAs, GMP investigations, Quality Risk Management (QRM).

Responsibilities

  • Successfully working within a multi-disciplinary team coordinating and delivering project activities meeting schedule, budgetary and quality expectations of the client.
  • Customarily and regularly exercises discretionary and independent judgment in performing the job.
  • Participate in training to ensure continued accreditation.
  • Maintain a safe working environment for self, team members and client staff.
  • Other tasks in alignment with your skills and competencies as required by the project, client and/or management.

Essential Qualities

  • Excellent organizational, verbal, and written communication skills; with demonstrated ability to efficiently and effectively, communicate with cross-functional teams and management on recommended course of action, with minimal assistance.
  • Proficient computer skills and be experienced using MS Office software (Word, Excel, and PowerPoint) and MS Project (as needed).
  • A self-starter, detail oriented and able to work independently with minimal supervision.
  • Excellent troubleshooting skills: ability to react quickly to understand and solve problems.

Education & Experience Requirements

B.S. degree in Biology, Biochemistry, Chemistry, Engineering, or equivalent years’ experience working in FDA-regulated industries.

Please note that only local candidates will be considered.

Job Summary

The candidate will be a part of the ICQ Consultants team and will be responsible for the project management activities for small to large projects.

Required Skills

  • 2 to 6 years of Project Management (PM) with experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device industry.
  • Experience in scheduling, budgeting, planning, resource loading and overall oversight for the execution of CQV projects for lab processes, equipment and utilities process used in the Biotech or Pharmaceutical Industry.
  • Direct experience within the following areas: Project management (PM), P6, Installation and Operational Qualification (IQ, OQ) protocols, Validation, Standard Operating Procedure (SOP), Change Control, Data Analysis, single use technologies.

Responsibilities

  • Successfully working within a multi-disciplinary team coordinating and delivering project activities meeting schedule, budgetary and quality expectations of the client.
  • Customarily and regularly exercises discretionary and independent judgment in performing the job.
  • Participate in training to ensure continued accreditation.
  • Maintain a safe working environment for self, team members and client staff.
  • Other tasks in alignment with your skills and competencies as required by the project, client and/or management.

Essential Qualities

  • Excellent organizational, verbal, and written communication skills; with demonstrated ability to efficiently and effectively, communicate with cross-functional teams and management on recommended course of action, with minimal assistance.
  • Proficient computer skills and be experienced using MS Office software (Word, Excel, and PowerPoint) and MS Project (as needed).
  • A self-starter, detail oriented and able to work independently with minimal supervision.
  • Excellent troubleshooting skills: ability to react quickly to understand and solve problems.

Education & Experience Requirements

B.S. degree in Biology, Biochemistry, Chemistry, Engineering, or equivalent years’ experience working in FDA-regulated industries.

Please note that only local candidates will be considered.

That’s What I Love About ICQ

“What I love most about working at ICQ is the feeling of family. The company genuinely cares about its employees’ success and supports our career growth with personalized mentorship. The little things don’t go unnoticed — the senior leadership team regularly stops to ask how employees are doing, and they are always accommodating to our location and commuting needs when on assignment.”

Ryan Hart
Managing Consultant
Joined ICQ in 2016

Looking for a Great Opportunity?

Find Your Home at ICQ

We have something to offer everyone working in the CQV lifecycle — whether you’re an engineer or scientist, entry-level or senior, East Coast or West.

The best benefits package in our space. Seriously.

  • 401k
  • Health, Dental, Vision Insurance
  • Life Insurance
  • Paid Holidays
  • Vacation
  • Short- and Long-Term Disability