ZipRecruiter

Log In

2

Entry Level Chromatography Sales Jobs (NOW HIRING)

W.R. Grace & Co.

Sr Technician Specialist

Columbia, MD · On-site

$65 - $85/hr

Provides technical support to Sales, Marketing, Technical Service and Manufacturing organizations ... Experience with Gas Chromatography-Mass Spectrometry (GC-MS). * Experience with edible oils ...

All JobsBusiness JobsSales JobsSales Professional JobsEntry Level Chromatography Sales Jobs

Entry Level Chromatography Sales information

See salary details

$22K

$45K

$65K

How much do entry level chromatography sales jobs pay per year?

As of Sep 4, 2026, the average yearly pay for entry level chromatography sales in the United States is $45,046.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,000.00 and $50,000.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of Chromatography Sales jobs?

The most popular types of Chromatography Sales jobs are:

Entry Level Chromatography Sales jobs near you

CIP Engineer / Consultant

Stark Pharma Solutions Inc

Boulder, CO • On-site

Contractor

Posted 25 days ago

Job description

Position: CIP Engineer / Consultant
Location: Colorado
Duration: Long Term
 

Job Overview

We are seeking an experienced CIP Engineer / Consultant to support cleaning cycle development, commissioning, qualification, and validation activities within a pharmaceutical/GMP manufacturing environment. The ideal candidate will have strong hands-on experience with CIP systems and circuits, cleaning validation, process equipment, and pharmaceutical manufacturing systems.

Key Responsibilities

  • Develop and optimize Clean-in-Place (CIP) cleaning cycles for process vessels and lines, chromatography skids/columns, UF/DF skids, centrifuges, glass/parts washers, and portable processing equipment.
  • Perform commissioning activities and provide automation support for CIP systems, including PLC and SCADA/DeltaV systems.
  • Develop, execute, and document cleaning validation protocols and generate summary reports.
  • Prepare and maintain documentation in accordance with Good Documentation Practices (GDP).
  • Consult with clients and vendors regarding technical issues, major problems, and project developments.
  • Review engineering specifications for compliance with applicable engineering requirements and standards.
  • Perform batch record reviews, including verification of calibration and in-process data.
  • Review piping designs and flow calculations for CIP systems.
  • Support troubleshooting and resolution of CIP system and circuit issues.
  • Support commissioning, qualification, and validation of pharmaceutical manufacturing equipment.
  • Provide technical support for CIP cycle development, optimization, and cleaning processes.

Required Qualifications

  • Minimum 3 years of pharmaceutical manufacturing or GMP environment experience.
  • Bachelor's degree in Chemical Engineering or a related field.
  • Hands-on experience with CIP systems and CIP circuits.
  • Experience with cleaning validation, protocol development, execution, and summary reports.
  • Experience with CIP troubleshooting is preferred.
  • Familiarity with cleaning of pharmaceutical process equipment, CIP cycle development and optimization, piping design, and fluid dynamics.
  • Minimum 3 years of Commissioning, Qualification, and Validation (CQV) experience with pharmaceutical manufacturing equipment.
  • Familiarity with PLC and SCADA/DeltaV plant control systems.
  • Strong written and verbal communication skills.
  • Strong computer skills, including Microsoft Office.
  • Willingness to travel as required.