ICQ will be attending the PDA New England Chapter Dinner Event and Facility Tour.

dinner meeting.pngPlease join ICQ for the next New England PDA Dinner Meeting.  The meeting “Future Trends in Manufacturing” with Venkatesh Natarajan and Aaron Noyes will be held on Wednesday, March 14th at Millipore Sigma in Burlington MA.

NEPDA is offering an opportunity to visit MilliporeSigma’s new, state of the art M LabTM Collaboration Center in Burlington, MA. Inside the M LabTM, you can see pilot and process development labs containing biomanufacturing equipment used in multiple unit operations including upstream single-use bioreactors and clarification tools as well as downstream chromatographic purification and tangential flow concentration systems. The M LabTM Collaboration Center is a place where visitors have the freedom to explore applications and run experiments in an innovative, non-GMP environment.

ICQ will be a gold sponsor and we would love to connect with you at the event!

facebookbannerJoin our network, follow us and share this on LinkedIn, Google +, Twitter and Facebook so you can see other new and exciting news and discussions being posted by ICQ Consultants.

Be part of an extraordinary team. ICQ is recruiting Process Validation Engineers in the Greater Boston Area.

If you are considering a career change, we would love to hear from you.  ICQ is actively recruiting highly motivated professionals to join our team.  We currently have opportunities available in Greater Boston.

ICQ offers some of the most competitive benefits and wages in our segment of service providers which include the following:

    • Short term / Long Term Disability – Paid 100% by ICQ
    • Life insurance – Paid 100% by ICQ
    • Tufts Health Insurance, Dental and Vision Plan – Paid 100% by ICQ
    • Paid time off for Holidays, Sick Time and Vacation
    • 401K with a 100% match to the first 4%

Positions report to the assigned manager and applicants are responsible for developing and executing protocols, including test functions, calibration, and sampling.  Must maintain compliance with the company’s Standard Operating Procedures and Policies.


  • BS/BA degree in Biology, Biochemistry, Chemistry, Engineering or related experience in FDA-regulated industries working in QC, Manufacturing, Engineering, QA and/or Validation.
  • Experience or a demonstrated ability to perform the responsibilities of the position in leading, planning, and execution of projects involving one or more of the following:
    • 3 to 5 years QC Lab Validation Experience.
    • 2 to 5 years Computer System Validation (Process Automation)
    • 2 to 5 years Commissioning, Qualification and Validation of Utilities, Facilities, Processes and Process Equipment


  • Develop and execute validation plans, test plans, validation protocols, and procedures.
  • Customarily and regularly exercises discretionary powers and independent judgment in performing the job.
  • Work as a leader, part of validation team, or independently to develop protocols and procedures, execute same including test functions, sampling, and calibration.
  • Communication with management, clients, and project team members.
  • Participate in training to ensure continued accreditation.
  • Other tasks as required by department management.
  • Travel may be required.


  • QC Lab Commissioning/Qualification/Validation
  • Process Validation – General Principles and Practices
  • Computer System Validation (Automation – Delta V)
  • Commissioning, Qualification and Validation Generalist (Facilities, Utilities, Process Equipment etc.)
  • Strong Attention to Detail
  • Proficient in MS Word and MS Excel
  • Excellent Communication Skills
  • Ability to handle many tasks with limited direction
  • Ability to deliver results is a must

Only local candidates will be considered.

If you are interested in learning more about current opportunities, contact us directly at resumes@icqconsultants.com