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Jurata Thin Film is a privately held biotechnology company that is revolutionizing the way vaccines and other biological medicines are stored, transported, and distributed. Our thin film technology, which stabilizes biological therapeutic payloads at ambient temperature, is disrupting the current cold-chain distribution ecosystem on which many life-saving biological drugs are currently dependent. We are seeking a Research Associate to join our team. This is an exciting opportunity to help develop a disruptive technology that will change the way critical therapeutics are distributed to those that need them around the world. As an early addition to the research team, input and direction will be a critical expectation of this hire. Therefore, while this requisition specifically seeks expertise in Biological Formulations, we are also looking for an individual who is capable of wearing multiple hats, has a multidisciplinary background, and comfortable delving into areas outside of their comfort zone (i.e., a life-long learner).
Job Description:
1. Perform bioanalytical assays like C12, Luciferase, Western blot, ELISAs and PCR.
2. Conduct routine physical and chemical tests, such as pH measurement, viscosity determination, Karl Fisher’s titration, enumeration, according to approved procedures and compendial methods (e.g., USP, EP, JP).
3. Record test results accurately and timely in laboratory notebooks, electronic systems, and quality records, ensuring compliance with good documentation practices (GDP) and regulatory requirements.
4. Record test results accurately and timely in laboratory notebooks, electronic systems, and quality records, ensuring compliance with good documentation practices (GDP) and regulatory requirements.
5. Investigate and troubleshoot deviations, out-of-specification (OOS) results, and laboratory incidents by conducting root cause analysis, implementing corrective and preventive actions (CAPAs), and documenting findings in investigation reports.
6. Support method transfer, method validation, and stability testing activities by executing protocols, analyzing samples, and interpreting data in accordance with regulatory guidelines and industry best practices.
7. Maintain and calibrate laboratory equipment, instruments, and analytical systems, ensuring their proper functioning, accuracy, and traceability to established standards.
8. Assist in the qualification and validation of analytical methods, equipment, and facilities by participating in validation protocols, executing validation studies, and generating validation reports as required.
9. Collaborate with cross-functional teams to address quality-related issues, implement quality improvements, and support continuous process improvement initiatives.
10. Review and update standard operating procedures (SOPs), test methods, and quality control documentation to ensure alignment with current regulations, industry standards, and best practices.
We offer competitive compensation based on qualifications and experience, as well as opportunities for professional growth and development. If you are passionate about scientific research and eager to contribute to cutting-edge projects in the field of Biotechnology, we encourage you to apply.
Job Type: Full-time
Pay: $60,000.00 - $70,000.00 per year
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Work Location: In person
Full Time
$97k-127k (estimate)
03/29/2024
04/24/2024
The job skills required for Quality Control Specialist include Quality Control, Microsoft Office, Problem Solving, Biochemistry, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality Control Specialist. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Quality Control Specialist. Select any job title you are interested in and start to search job requirements.
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Quality Assurance (QA) Specialist duties and responsibilities Providing management and control of the quality assurance processes Maintaining the quality of products.
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These roles require highly organized specialists with meticulous attention to detail.
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Monitor Critical Control Points.
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