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Entry Level Quality Assurance Biotech Jobs in Raleigh, NC

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How much do entry level quality assurance biotech jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for entry level quality assurance biotech in Raleigh, NC is $28.47, according to ZipRecruiter salary data. Most workers in this role earn between $18.22 and $33.41 per hour, depending on experience, location, and employer.

What is an entry level quality assurance professional in biotech?

Entry level quality assurance (QA) jobs in biotech involve ensuring that products and processes meet regulatory, industry, and company standards. Employees in these roles may review documentation, assist with audits, monitor manufacturing processes, and support the implementation of quality systems. They often work closely with other departments to ensure compliance and continuous improvement. These positions typically require attention to detail, knowledge of Good Manufacturing Practices (GMP), and strong organizational skills. Entry level QA roles are a great starting point for understanding quality systems in the biotech industry.

What are the key skills and qualifications needed to thrive as an entry level quality assurance professional in biotech?

To thrive as an Entry Level Quality Assurance professional in biotech, you typically need a bachelor's degree in a life science or related field, a solid grasp of laboratory practices, and knowledge of regulatory standards like GMP or GLP. Familiarity with quality management systems (QMS), document control software, and laboratory information management systems (LIMS) is often required. Attention to detail, strong organizational skills, and effective communication are essential soft skills for this role. These skills and qualifications ensure accurate compliance, reliable documentation, and effective collaboration, which are critical for maintaining product quality and regulatory approval in the biotech industry.

What types of projects and team collaborations can I expect as an entry level quality assurance professional in biotech?

As an Entry Level Quality Assurance professional in biotech, you will typically work closely with cross-functional teams such as manufacturing, research and development, and regulatory affairs. Your daily responsibilities may include reviewing documentation, monitoring processes for compliance, and assisting with internal audits. Collaboration often involves communicating findings, helping to resolve quality issues, and supporting continuous improvement initiatives. This teamwork helps you build a strong understanding of both regulatory standards and company protocols, which can open doors to advanced QA or specialized roles in the future.

What are the most commonly searched types of Quality Assurance Biotech jobs in Raleigh, NC?

The most popular types of Quality Assurance Biotech jobs in Raleigh, NC are:

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For Entry Level Quality Assurance Biotech jobs in Raleigh, NC, the most frequently searched job titles are:

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The top searched job categories for Entry Level Quality Assurance Biotech jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Entry Level Quality Assurance Biotech jobs?

Cities near Raleigh, NC with the most Entry Level Quality Assurance Biotech job openings:

Infographic showing various Entry Level Quality Assurance Biotech job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $59,224 per year, or $28.5 per hour.

Senior Associate Manufacturing - Technical Training - Upstream Bulk Drug Substance

Amgen, Inc.

Holly Springs, NC โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago


Job description

Career Category
Manufacturing
Job Description
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of.
Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX batch facility will combine the latest in single use technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.
Senior Associate Manufacturing - Technical Training - Upstream Bulk Drug Substance
Live
What you will do
Let's do this. Let's change the world. In this vital role, you will be a key member of the team that develops and facilitates training and the Human and Organizational Performance (HOP) philosophy in the Amgen North Carolina Biologics Drug Substance Manufacturing plant. We are looking for a talented Manufacturing team member to help deliver opportunities for reliability, efficiency, agility and differentiation for the ANC Manufacturing plant.
This individual contributor position reports into the Senior Manager of the MFG Technical Training team and interacts broadly across the site to implement key training and (HOP) deliverables, quality initiatives. This role will focus on supporting manufacturing training on and off the floor and supporting investigations when necessary. The flexibility to support all four shifts covering 24/7 operations is a requirement.
Responsibilities include:
  • Supporting the development and execution of the manufacturing training strategy, ensuring operational readiness and efficient time to contribution.

  • Providing training expertise for MFG area of responsibility (i.e. cell culture, purification, MFG Services).

  • Leading and organizing MFG New Hire Orientation, ensuring content is up to date and relevant.

  • Performing Job Task Analysis on the floor to determine where Performance Supporting Materials (SOP updates, videos, one-slide updates etc.) are needed and then creating Performance Supporting Materials to create a best-in-class training program.

  • Supporting Manufacturing teams during complex investigations and change controls.

  • Use operational Learning Team strategies to promote open collaboration with staff to maximize learning opportunities and investigation findings.

  • Support annual requalification programs for manufacturing to ensure training compliance.

  • Maintain accurate Training Assignment Profiles and Assignment Vehicles for Manufacturing areas.

  • Serve as Learning Management System SME and first stop for questions from MFG staff and management about the training program.

  • Present complex topics to large and small groups at various levels and quickly understand and clearly communicate complex issues.

  • Build effective relationships across functions.

  • Navigate through ambiguity and provide a structured problem-solving approach.

Win
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The collaborative investigator we seek has a biologics Drug Substance manufacturing and investigations background with strong cross-functional project management and communication skills as well as the below qualifications.
Basic Qualifications:
Master's degree
OR
Bachelor's degree and 6 months of Manufacturing or Operations experience
OR
Associate's degree and 2 years of Manufacturing or Operations experience
OR
High school diploma / GED and 4 years of Manufacturing or Operations experience
Preferred Qualifications:
  • 5+ years related work experience (manufacturing, process development, or quality assurance) in biotech or pharmaceutical industry with progressively increasing responsibility

  • Experience in training development and facilitation

  • Training content creation expertise in systems

  • SOP writing & technical writing skills

  • Experience working in Learning Management Systems

  • Degree in Science or Engineering
  • Experience with Aseptic techniques and laminar flow hood operation.

  • Experience using Quality Management Systems (i.e. Track Wise or Veeva) for Deviation investigations and CAPAs

  • Demonstrated project management ability

  • Experience presenting to inspectors during regulatory inspections and internal audits.

  • Excellent written and verbal communication skills

  • Ability to work in a team matrix environment and build relationships with partners

  • Strong interpersonal skills

Thrive
What you can expect of us
The annual salary range for this opportunity in the U.S. is [HR to input market pay range].
In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:
  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

  • Stock-based long-term incentives

  • Award-winning time-off plans and bi-annual company-wide shutdowns

  • Flexible work models, including remote work arrangements, where possible

Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
#AmgenNorthCarolina
Salary Range
86,048.05USD -116,417.95 USD