Amgen

66 Amgen Senior Associate Quality Control Jobs Hiring Near You

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Amgen Jobs Information

What is it like to work at Amgen?

Amgen is a biotechnology company that values innovation, collaboration, and patient-centricity, fostering a culture that encourages open communication and teamwork among its employees. The company's research and development teams work in a dynamic environment, often in collaboration with external partners and academia, to develop and deliver life-changing medicines to patients with serious diseases. Working at Amgen may appeal to candidates who are passionate about advancing medical science and improving human health, as the company offers opportunities for professional growth, mentorship, and contributions to groundbreaking research.

What makes Amgen an attractive place to work?

Amgen is a leading biotechnology company that has been at the forefront of innovation in the pharmaceutical industry for decades, with a strong focus on developing life-changing medicines for patients with serious diseases. The company's work environment is characterized by a culture of collaboration, innovation, and scientific excellence, with opportunities for employees to work on cutting-edge projects and contribute to groundbreaking research. As a result, Amgen offers a dynamic and challenging work environment that can provide employees with opportunities for professional growth, development, and impact in the field of biotechnology.
Infographic showing various Senior Associate Quality Control job openings at Amgen in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Associate Quality Control

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Holly Springs, NC • On-site

Contractor

Re-posted 24 days ago


Job description

Duration: 12+ Months
Shift
: Fully Onsite - Standard hours - Up to 5 days per month may require shift flexibility.
Job Description:
We are seeking a highly motivated and experienced Associate in Quality Control (QC) Chemistry to support the startup and operational readiness of our QC laboratory. Working with minimal supervision, this individual will lead and contribute to critical activities including system qualifications, method transfers, and laboratory operations in a GMP-regulated environment.
Key Responsibilities:
  • Collaborate cross-functionally with site teams to implement work order and preventative maintenance systems for laboratory equipment.
  • Review and contribute to validation documentation to support onboarding of equipment and computerized systems.
  • Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical assessments, validation reports, trend reports, and safety evaluations.
  • Assist in the procurement of laboratory consumables and critical reagents required for startup activities.
  • Coordinate and execute training and method transfer activities for instruments including H/UPLC, TOC, Conductivity, Osmolality and other chemistry-based platforms.
  • Actively participate in audits, quality initiatives, and cross-functional projects with site or global impact.
  • Provide routine operational support during weekends and public holidays as required.
 
Preferred Qualifications:
  • Bachelor's degree or higher in Chemistry, Compendial testing or a related scientific discipline.
  • Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment, with a strong background in analytical testing.
  • Proficient in analytical laboratory techniques and instrumentation.
  • Familiarity with laboratory systems such as LIMS and LMES/CIMS.
  • Demonstrated understanding of industry regulations, data integrity, and compliance standards.
  • Strong technical writing, documentation, and communication skills.
  • Experience with method validation, verification, and transfer.
  • Excellent interpersonal skills with the ability to collaborate across teams and adapt to varying communication styles.
 
Basic Qualifications:
  • High school/GED + 2 years work experience or
  • Associates degree and 6 months work experience or
  • Bachelors degree
 
Top must have skills:
  • Must have a chemistry background
  • GMP experience
  • Empower experience
 
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