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Entry Level Biotech Patent Analyst Jobs (NOW HIRING)

Novartis

IP Search & Analytics Manager

Cambridge, MA · Hybrid

$138K - $257K/yr

Conduct patent and scientific literature searches to support critical intellectual property and ... Knowledge of pharmaceutical, biotechnology, healthcare, or related life sciences industries is a ...

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AbbVie

Corporate Counsel-Patent

North Chicago, IL

Conduct prior art searches, analyze third-party patent positions, and conduct due diligence to ... Technical degree in relevant field, such as molecular biology, biotechnology, biochemistry, biology ...

Legend Biotech US

Sr. Scientist

Philadelphia, PA · On-site

$92K - $126K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Measure transduction rate using flow and VCN analysis. * Generate, manage, evaluate, and maintain ...

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How much do entry level biotech patent analyst jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for entry level biotech patent analyst in the United States is $27.77, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $30.05 per hour, depending on experience, location, and employer.
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Entry Level Biotech Patent Analyst jobs near you
Infographic showing various Entry Level Biotech Patent Analyst job openings in the United States as of August 2026, with employment types broken down into 55% Full Time, 27% Part Time, 9% Temporary, and 9% Contract. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $57,761 per year, or $27.8 per hour.

Quality Control Laboratory Analyst (Raw Materials)

Krystal Biotech

Pittsburgh, PA • On-site

$23.25 - $31.25/hr

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.
Position Overview:
Krystal Biotech, Inc is seeking a highly motivated Quality Control Analyst who will be responsible for in-house raw materials and product testing for the use in the manufacture of clinical and commercial drug products.
Primary Responsibilities:
  • Perform cGMP material inspection for all materials utilized for drug product manufacturing.
  • Perform cGMP material testing for all materials needed for further use in manufacturing process.
  • Review analytical data for compliance with regulations, methods and other specifications or criteria and collaborate with management when data does not meet acceptance criteria.
  • Participate in laboratory investigations, quality event investigations, protocol and report development.
  • Initiate and update quality control documentation, such as SOPs, material monographs (specification and testing documents), and test methods.
  • Support activities for Document Control and Record Retention.
  • Implementation of USP Quality Standards and verification of USP Methods.
  • Maintain equipment in the QC Lab by performing and coordinating equipment qualification, calibration, and preventive maintenance.
  • Other duties as assigned.
Requirements and Preferred Qualifications:
  • Bachelor's degree in life sciences or equivalent.
  • Experience with pH, Osmo, Endotoxin, Appearance, customized media, cell culture, and FBS testing, preferred.
  • Demonstrated experience in laboratory environment and ability to follow SOPs.
  • A demonstrated self-starter who is highly motivated and able to address changing priorities.
  • Ability to take a proactive approach on the job with the ability to work with a dynamic team.
  • Excellent scientific writing, other written and oral communication skills are required.
  • Proficient in Microsoft Word, Excel and PowerPoint.

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.

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