
Quality Control Laboratory Analyst (Raw Materials)
Krystal BiotechPittsburgh, PA
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Overview
Schedule
Full-time
Career level
Senior-level
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.
- 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.
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FAQs About Quality Control Laboratory Analyst (Raw Materials) Jobs at Krystal Biotech
What is the work location for this position at Krystal Biotech?
This job at Krystal Biotech is located in Pittsburgh, PA, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Krystal Biotech?
Employer has not shared pay details for this role.
What employment applies to this position at Krystal Biotech?
Krystal Biotech lists this role as a Full-time position.
What experience level is required for this role at Krystal Biotech?
Krystal Biotech is looking for a candidate with "Senior-level" experience level.
What is the process to apply for this position at Krystal Biotech?
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