ZipRecruiter

Log In

1

Biotech Recruiters In Jobs (NOW HIRING)

IQVIA

CRA 2, Oncology, IQVIA Biotech

Durham, NC

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

IQVIA

CRA 2, Oncology, IQVIA Biotech

Fort Worth, TX

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

IQVIA

CRA 2, Oncology, IQVIA Biotech

Austin, TX

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

IQVIA

CRA 2, Oncology, IQVIA Biotech

Houston, TX

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

IQVIA Argentina

NY · On-site

$125 - $150/hr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

New

IQVIA

CRA 2, Oncology, IQVIA Biotech

New York, NY

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

IQVIA

CRA 2, Oncology, IQVIA Biotech

Houston, TX

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

IQVIA

CRA 2, Oncology, IQVIA Biotech

New York, NY

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

IQVIA Argentina

$125 - $150/hr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

New

IQVIA

CRA 2, Oncology, IQVIA Biotech

Fort Worth, TX

$74K - $175K/yr

IQVIA Biotech is expanding our Clinical Monitoring team and is seeking CRA 2 professionals with a ... the recruitment process will result in immediate disqualification of your application, or ...

previous page

Showing results 41-60

All JobsBusiness JobsHuman Resources JobsHuman Resources Professional JobsBiotech Recruiters In Jobs

Biotech Recruiters In information

See salary details

$12

$27

$44

How much do biotech recruiters in jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for biotech recruiters in in the United States is $27.23, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $31.97 per hour, depending on experience, location, and employer.
More about Biotech Recruiters In jobs

What cities are hiring for Biotech Recruiters In jobs?

Cities with the most Biotech Recruiters In job openings:

What states have the most Biotech Recruiters In jobs?

States with the most job openings for Biotech Recruiters In jobs include:

What are popular job titles related to Biotech Recruiters In jobs?

For Biotech Recruiters In jobs, the most frequently searched job titles are:

Biotech Recruiters In jobs near you

Quality Assurance Associate

Pittsburgh, PA • On-site

Krystal Biotech
Biotechnology Research and Development • 51 - 200 employees
Learn more about Krystal Biotechexternal

Full-time

Re-posted 11 days ago

Job description

About Krystal Bio:
At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.
Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient's end-to-end experience.
Krystal received U.S. FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.
Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan. We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.
Job Description Summary:
Krystal Biotech, Inc. is seeking a highly motivated and experienced Quality Associate to support quality systems, GMP manufacturing processes and documentation practices at our headquarters in Pittsburgh's South Side.
Primary Responsibilities:
  • Work with internal teams to obtain an understanding of the product and the documentation requirements.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended use.
  • Develop expertise on FDA regulations and audit processes.
  • Initiate and update GMP manufacturing associated documentation, such as clearing procedures.
  • Provide oversight of daily QA functions which include review and approval of records generated by manufacturing and quality control documents.
  • Provide support for updates on standard operating procedures and associated forms.
  • Assist with QA efforts for site cGXP documentation related to the operation of gene therapy manufacturing.
  • Ensure compliance with regulatory agencies and oversee continuous improvement of company's QA and compliance functions.
Requirements & Desired Competencies:
  • Minimum of a Bachelor's Degree (Biology or related Life Science) with 3+ years of relevant quality systems experience in the biotech or pharmaceutical industry.
  • Background that includes knowledge/experience in GMP, GLP, and GCP.
  • Experience with FDA audits is highly preferred.
  • Strong knowledge of GMP and ICH requirements.
  • Must be a self-starter and capable of working with minimal oversight.
  • Must be able to handle multiple roles and work in a fast paced and changing environment and know how to prioritize activities appropriately.
  • Excellent oral and written communication skills.

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.
xcld121

Apply