Corden Pharma - A Full-Service CDMO
Corden Pharma - A Full-Service CDMO
Corden Pharma - A Full-Service CDMO is a global pharmaceutical contract development and manufacturing organization serving clients from early clinical programs through commercial production. Its integrated capabilities span active pharmaceutical ingredients (APIs), drug products, and lipid excipients, with specialist expertise in peptides, oligonucleotides, lipid nanoparticle (LNP) formulation, highly potent and oncology compounds, sterile and non-sterile dosage forms, and custom lipid manufacturing. The company supports pharmaceutical development and supply through cGMP facilities across Europe and North America, combining technical manufacturing services with integrated project management.

Senior IPC QC Analyst

Perform routine and advanced quality control testing at Corden Pharma’s Boulder pharmaceutical manufacturing site. Maintain GMP compliance, troubleshoot laboratory instruments, and review analytical data.

Description

  • Analyze routine and non-routine samples using routine and advanced methods
  • Partner with Process and QC Chemists to resolve issues and train new technicians
  • Calibrate equipment, standardize titrants, and validate standards
  • Identify and resolve QC laboratory instrument issues
  • Report process, procedure, and material issues and proposed solutions to QC Chemists
  • Investigate anomalous test results and take corrective action
  • Keep the laboratory clean and organized in line with safety, regulatory, and chemical hygiene policies
  • Troubleshoot QC laboratory instruments and analytical methods
  • Complete daily records in SAP and LIMS
  • Print labels, review certificates of analysis, and approve final products
  • Compile data for statistical process control and modify LIMS
  • Conduct peer reviews of analytical data
  • Manage the generation and accumulation of hazardous and non-hazardous waste
  • Attend QC team meetings and build team skills
  • Lead the shift when management is absent
  • Write and revise SOPs and methods as assigned
  • Support cGMP-compliant pharmaceutical manufacturing within Corden Pharma Colorado’s Quality Management System

Requirements

  • Hold a bachelor’s degree in a related science and have five years of GMP experience in a quality laboratory; alternatively, have five years of related experience in a quality environment or an equivalent combination of education and experience
  • Read and interpret safety rules, operating and maintenance instructions, and procedure manuals
  • Write routine reports and correspondence
  • Speak effectively to groups of customers or employees
  • Work with probability, statistical inference, geometry, trigonometry, fractions, percentages, ratios, and proportions
  • Solve practical problems and interpret written, oral, diagram, or schedule instructions
  • Bring strong analytical skills and knowledge of general or organic chemistry
  • Apply specialized skills to non-routine methods
  • Demonstrate mechanical aptitude with laboratory equipment
  • Analyze data at an advanced level and detect errors
  • Demonstrate problem-solving skills
  • Commit to QSHE principles
  • Write and revise SOPs and methods as directed
  • Use laboratory software at an advanced level
  • Work 12-hour rotating day or night shifts, including weekends and holidays
  • Use word processing, spreadsheets, email, and database applications confidently
  • Occasionally lift and/or move up to 25 pounds
  • Comply with safety, regulatory, chemical hygiene, GLP, GMP, FDA, ICH Q7, and applicable global regulatory requirements

Benefits

  • 401(k) matching: Corden Pharma contributes 100% of the first 6%; fully vested after two years of service
  • Accident plan
  • Critical illness insurance
  • Dental insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account
  • PPO/HSA health insurance
  • Hospital indemnity plan
  • Identity theft protection
  • Life insurance
  • Paid parental leave
  • Tuition reimbursement
  • Wellness program
  • Three weeks of vacation in the first year
  • Vision insurance

Related Jobs

ReSus Consult GmbH

Sales Director, HVAC and Plumbing (SHK)

ReSus Consult GmbH
DEGermany
€120,000 – €180,000 / year
HybridFull-timeLeadGerman RequiredSales

Lead a regional portfolio of five to twelve SHK trade businesses, with responsibility for budgets and operational development. Build regional collaboration through digitalization, shared capacity, larger projects and best-practice exchange.

Open
smartkündigen OHG

Senior Sales Manager (German-speaking), Remote

smartkündigen OHG
11 – 50 Employees
B2CProductivitySaaS

Advise customers, grow existing accounts, and close sales for smartkündigen’s digital contract cancellation service. Work fully remotely without cold calling.

Open
smartkündigen OHG

Senior Sales Manager, Remote

smartkündigen OHG
11 – 50 Employees
B2CProductivitySaaS

Advise customers, grow existing accounts, and close sales for smartkündigen’s digital contract cancellation service. Work fully remotely worldwide, handling inbound inquiries without cold calling.

Open