Senior Technical Associate

Posted 10 Days Ago
Be an Early Applicant
Germantown, MD, USA
In-Office
45K-50K Annually
Senior level
Biotech
The Role
Perform bulk formulation and production of molecular biology products in a regulated laboratory environment. Operate, maintain, and calibrate laboratory equipment; complete batch records and production documentation; troubleshoot deviations and quality issues; support SOP, specification, corrective-action, and process-improvement updates; and maintain compliance with quality, safety, environmental, ISO, FDA, and OSHA requirements.
Summary Generated by Built In

Overview 

 
At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible.  

We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams. 
 
We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. 

 

At QIAGEN, every day is an opportunity to make a real-life impact. 

 

Join us, grow with us, and together, let's shape the future of biological discovery. 

About the Opportunity
At QIAGEN, you will play an important role in supporting the production of molecular biology products within a regulated laboratory environment. In this position, you will perform routine bulk formulation and production activities according to established procedures while ensuring compliance with quality, safety, and regulatory standards. Working in a fast-paced environment, you will collaborate with colleagues to maintain high standards of quality, efficiency, and safety while helping QIAGEN deliver trusted solutions to customers worldwide.
Your Tasks Include
  • Perform scheduled bulk formulation and production activities according to approved procedures and applicable regulations.
  • Accurately complete production documentation, batch records, and labor reports in a timely manner.
  • Operate, maintain, and calibrate standard laboratory equipment to support daily production activities.
  • Identify, communicate, and assist in troubleshooting production issues, discrepancies, or deviations that may impact product quality or data integrity.
  • Support the review of documentation and assist with updating SOPs, specifications, corrective actions, and process improvement initiatives.
  • Contribute to departmental and organizational goals through collaboration, efficiency, and continuous improvement efforts.
  • Ensure ongoing compliance with applicable quality, environmental, health, and safety regulations and standards, including ISO, FDA, OSHA, and other relevant requirements.
Your Profile
  • Associate's or Bachelor's degree in a scientific discipline, or an equivalent combination of education and experience, with 1-2 years of relevant laboratory or production experience.
  • Ability to apply scientific principles and laboratory techniques within a production environment while working under guidance and supervision.
  • Experience with general laboratory equipment and proficiency in basic Microsoft Office applications.
  • Strong organizational skills with attention to detail and the ability to manage equipment, materials, and time effectively.
  • Ability to accurately complete production documentation and prepare basic technical records.
  • Comfortable working with potentially biohazardous and/or chemically hazardous materials while following established safety procedures.
  • Ability to adapt to changing priorities, work effectively within a team environment, and perform medium physical work, including lifting up to 50 lbs.
The estimated base salary range for this position is $45,000-$50,000. Compensation will be based on the candidate’s experience, skills, geographic location, and other job-related factors. In addition to base salary, we offer a total compensation package that includes a bonus plan and generous benefits.

What we offer 

 

  • Bonus/Commission  

  • Local benefits   

  • Referral Program  

  • Volunteer Day  

  • Internal Academy (QIALearn)   

  • Employee Assistance Program   

  • Hybrid work (conditional to your role) 

 

Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking.  

 

QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability. 

Skills Required

  • Associate's or Bachelor's degree in a scientific discipline, or equivalent combination of education and experience
  • 1-2 years of relevant laboratory or production experience
  • Ability to apply scientific principles and laboratory techniques in a production environment under guidance and supervision
  • Experience with general laboratory equipment
  • Proficiency in basic Microsoft Office applications
  • Strong organizational skills and attention to detail
  • Ability to manage equipment, materials, and time effectively
  • Ability to accurately complete production documentation and prepare basic technical records
  • Ability to work safely with potentially biohazardous and chemically hazardous materials
  • Ability to adapt to changing priorities and work effectively within a team environment
  • Ability to perform medium physical work, including lifting up to 50 pounds

QIAGEN Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about QIAGEN and has not been reviewed or approved by QIAGEN.

  • Flexible Benefits Flexible work options (hybrid or remote where roles allow), flexible hours, sabbaticals, and site-specific childcare support work–life fit. Programs are presented as available where roles allow, signaling adaptable benefit design.
  • Wellbeing & Lifestyle Benefits A global Employee Assistance Program for employees and immediate family, alongside broader wellbeing initiatives and community volunteering time, provides everyday support. Recognition for inclusive culture reinforces the emphasis on a supportive environment.
  • Parental & Family Support Paid parental leave positioned as above typical U.S. norms and family-oriented offerings (e.g., on-site childcare at some locations) enhance caregiver support. Reports of solid PTO and holidays further strengthen family time.

QIAGEN Insights

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The Company
HQ: Hilden
6,000 Employees
Year Founded: 1984

What We Do

QIAGEN is the leading global provider of Sample to Insight solutions that enable customers to gain valuable molecular insights from samples containing the building blocks of life. Our sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies make these biomolecules visible and ready for analysis. Bioinformatics software and knowledge bases interpret data to report relevant, actionable insights. Automation solutions tie these together in seamless and cost-effective workflows. QIAGEN provides solutions to more than 500,000 customers around the world in Molecular Diagnostics (human healthcare) and Life Sciences (academia, pharma R&D and industrial applications, primarily forensics).

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