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Hic Jobs in Colorado (NOW HIRING)

Hic information

What is the difference between Hic vs Medical Coder?

AspectHicMedical Coder
Required CredentialsCertification in HIC coding or related fieldsCertified Professional Coder (CPC) or equivalent
Work EnvironmentHospitals, clinics, insurance companiesHospitals, outpatient clinics, insurance companies
Industry UsageHealthcare billing and coding for HIC-specific proceduresMedical billing and coding across various specialties
Common Search IntentHic vs Medical CoderHic vs Medical Coder

HIC professionals focus on coding for healthcare information and billing specific to HIC systems, while Medical Coders handle a broader range of medical procedures and diagnoses. Both roles require certification and work in healthcare settings, but HIC roles are more specialized in health information coding systems.

What are popular job titles related to Hic jobs in Colorado? For Hic jobs in Colorado, the most frequently searched job titles are:
Infographic showing various Hic job openings in Colorado as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 5% Part Time, 2% Temporary, and 14% Contract. Highlights an 97% Physical, and 3% Hybrid job distribution.

Senior Process Engineer - Downstream (Biologics & Peptides)

Stark Pharma Solutions Inc

Boulder, CO • On-site

$107K - $139K/yr

Contractor

Re-posted 20 days ago


Job description

Job Title: Senior Process Engineer – Downstream (Biologics & Peptides)

Location: Boulder, CO (100% Onsite)

Duration: 6 Months + Extensions

Start Date: ASAP

Job Summary

We are seeking a Senior Process Engineer with strong expertise in downstream processing to support the development, scale-up, and commercialization of biologics and peptide-based therapeutics. This role will focus on designing, optimizing, and implementing purification processes and manufacturing systems within a GMP-regulated environment.

The ideal candidate will have hands-on experience with chromatography and tangential flow filtration (TFF) technologies, along with a proven track record supporting process scale-up, equipment qualification, and manufacturing startup activities.

Key Responsibilities

  • Lead downstream process development and optimization activities for biologics and peptide products
  • Design, specify, and support implementation of purification systems including chromatography and TFF skids
  • Support process scale-up from development through pilot and commercial manufacturing
  • Drive startup, commissioning, qualification, and troubleshooting of downstream manufacturing equipment
  • Develop and execute process validation and verification strategies aligned with GMP and regulatory requirements
  • Collaborate with MSAT, Upstream, Manufacturing, and Quality teams to ensure process robustness and consistency
  • Author and review technical documentation including process descriptions, validation protocols, and regulatory support documents
  • Serve as a technical SME for downstream purification operations and technologies
  • Mentor junior engineers and support continuous improvement initiatives

Required Qualifications

  • Bachelor’s, Master’s, or PhD in Chemical Engineering, Biochemical Engineering, or related field
  • 8+ years of experience in biopharmaceutical process engineering with strong downstream processing expertise
  • Hands-on experience with:
  • Chromatography systems (affinity, ion exchange, HIC, etc.)
  • Tangential Flow Filtration (TFF) systems
  • Experience supporting equipment startup, commissioning, and qualification activities
  • Strong understanding of process validation and GMP manufacturing environments
  • Experience supporting or leading tech transfer and process scale-up activities
  • Strong troubleshooting, communication, and cross-functional collaboration skills