Quality Control Technician

Vitrolife Group; Englewood (CO); On-site; USD 34,000 - 39,000; Full time

Job summary

Vitrolife Group is seeking a Quality Control (QC) Technician for a 6-month temporary assignment in Englewood, Colorado. The role supports QC and validation activities, performing environmental monitoring, in-process testing, raw material release testing, and lab documentation to ensure product quality in a regulated manufacturing environment.

Ideal candidates have at least 6 months in a QC or microbiology lab, with a high school diploma or GED; a Bachelor's degree in biology or related life

Qualifications

• High School Diploma or GED required.
• At least 6 months of QC/microbiology lab experience.
• Bachelor’s degree in Biology, Microbiology, Life Sciences or related field preferred.

Responsibilities

• Execute environmental monitoring for cleanrooms.
• Perform QC testing: in-process, bioburden, growth promotion, raw material release.
• Release raw materials and manage reference sample inventories.
• Support validation activities and projects.
• Record samples and results in laboratory software systems.
• Maintain quality systems and cGMP compliance.
• Participate in cross-functional process improvement initiatives.

Skills

Microbiology techniques

Quality systems

cGMP

Verbal & written communication

Organizational skills

Teamwork

Education

High School Diploma or GED

Bachelor's degree in Biology, Microbiology, Life Sciences, or related field

Job description

At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.

Location: On-site in Englewood, CO

Compensation: $25 to $28 per hour

Position Summary

We are seeking a motivated and detail-oriented Quality Control (QC) Technician for a 6-month temporary assignment. In this role, you will support Quality Control and validation activities by performing environmental monitoring, in-process testing, raw material release testing, and laboratory documentation. This position plays a direct role in ensuring product quality and compliance within a regulated manufacturing environment.

Essential Responsibilities

• Execute the environmental monitoring program for cleanroom environments.
• Perform Quality Control testing, including:
• In-Process Testing
• Bioburden Testing
• Growth Promotion Testing
• Raw Material Release Testing
• Release raw materials and maintain reference sample inventories.
• Support process validation activities and projects.
• Record samples, test results, and laboratory data in laboratory software systems.
• Maintain compliance with quality systems, SOPs, and cGMP requirements.
• Participate in cross-functional process improvement initiatives and project teams.
• Assist with laboratory documentation and recordkeeping.
• Perform other duties as assigned.

Qualifications

Education

• High School Diploma or GED required.
• Bachelor's degree in Biology, Microbiology, Life Sciences, or a related field preferred.

Experience

• At least 6 months of experience in a Quality Control laboratory, Microbiology laboratory, or related scientific field.

Skills & Competencies

• Knowledge of microbiology laboratory techniques and practices.
• Experience working within quality systems and cGMP-regulated environments.
• Strong verbal and written communication skills.
• Technical and scientific report-writing abilities.
• Excellent organizational skills and attention to detail.
• Ability to work independently and collaboratively in a team environment.

Work Environment

• 80% Laboratory/Cleanroom
• 20% Administrative and documentation activities

An offer of employment is contingent on the successful passing of a background check. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.

We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.