ZipRecruiter

Log In

1

Biotech Assistant Jobs (NOW HIRING)

PBS Biotech

Research Associate

Camarillo, CA · On-site

Join PBS Biotech and Help Shape the Future of Cell Therapy Location: Camarillo, CaliforniaWhere ... Perform experiments for bioprocess development, optimization, and characterization. * Assist in ...

Tuskegee University

Position Information Position Title Assistant/Associate Professor, Plant Biotechnology (Non-tenured) Job Summary This position must have sound/extensive knowledge and research experience in plant ...

Barclays

Equity Research Biotech, AVP

New York, NY · On-site

Assistant Vice President Expectations * To advise and influence decision making, contribute to ... Join Barclays as an Equity Research Biotech, AVP, where you'll have the chance to collaborate with ...

PSC Biotech

Validation Engineer

Columbus, OH · On-site

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Assist in the configuration, testing, and troubleshooting of automation and manufacturing-related ...

previous pagenext page

Showing results 21-40

All JobsBiotech JobsBiotech Assistant Jobs

Biotech Assistant information

What is a biotech assistant?

A Biotech Assistant supports scientists and researchers in biotechnology labs by conducting experiments, preparing materials, and maintaining equipment. They assist in data collection, documentation, and laboratory safety procedures. Their role helps advance research in areas like pharmaceuticals, agriculture, and genetics. Strong attention to detail and knowledge of lab techniques are essential for success in this position.

What does a biotech assistant do?

A typical day for a Biotech Assistant involves preparing and maintaining laboratory equipment, assisting with experiments, recording and analyzing data, and ensuring all safety procedures are followed. You may also be responsible for managing laboratory supplies, disposing of hazardous materials correctly, and collaborating closely with research scientists and other lab staff. The work is detail-oriented and often requires managing multiple tasks simultaneously. Teamwork and effective communication are important as you often support ongoing projects and help troubleshoot minor issues that arise during experiments.

What skills and qualifications are needed to thrive as a biotech assistant?

To thrive as a Biotech Assistant, you should have a background in biology or a related science, strong laboratory skills, and meticulous attention to detail, often supported by an associate's or bachelor's degree. Familiarity with laboratory equipment, safety protocols, and data management systems such as LIMS is typically required. Excellent organization, communication, and teamwork skills help you excel when supporting scientists and handling multiple tasks. These abilities are crucial for ensuring accurate experimental results, maintaining lab safety, and contributing to research success.

More about Biotech Assistant jobs
What cities are hiring for Biotech Assistant jobs? Cities with the most Biotech Assistant job openings:
What are the most commonly searched types of Biotech jobs? The most popular types of Biotech jobs are:
What states have the most Biotech Assistant jobs? States with the most job openings for Biotech Assistant jobs include:
What job categories do people searching Biotech Assistant jobs look for? The top searched job categories for Biotech Assistant jobs are:
Biotech Assistant jobs near you
Infographic showing various Biotech Assistant job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Quality Assurance Associate

Krystal Biotech

Pittsburgh, PA • On-site

Full-time

Re-posted 8 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

Powered by JazzHR

hwnTbCw1wL