Liquidia is deeply passionate and committed to the discovery, engineering, and development required to bring novel therapies to patients who need them most, and to the healthcare providers who care for them. Our current drive is toward improving the treatment of pulmonary arterial hypertension (PAH). We will continue to combine our proprietary, innovative PRINT® Technology with new and established medications, offering the potential for both better precision and improved clinical outcomes. Our team members include some of the industry’s top scientists, clinicians, business strategists, engineers, and pharmaceutical executives. We work together to help people lead longer, healthier, and happier lives.

Job Summary

We are looking for an Associate Scientist, Quality Control. In this “hands-on” role within the Quality Control Lab, the Associate Scientist will join a talented and collaborative team that welcomes input and suggestions to help continue Liquidia’s upward trajectory at the most exciting time in the Company’s history. Critical to success are a scientific laboratory background, ability to follow CGMP documentation requirements, and excellent communication skills. The Associate Scientist will conduct laboratory analysis of raw materials and intermediates in support of Liquidia’s lead product candidate.

Job Responsibilities

• Execute laboratory testing according to established specifications or as defined by senior scientific staff members.
• Use strong observational and analytical skills to analyze experiments and draw conclusions from results.
• Report results to fellow team members, supervisor, and other appropriate stakeholders.
• Document experiments in laboratory notebooks and in appropriate quality systems in accordance with CGMP.
• May perform technical review of fellow team members’ laboratory documentation.
• Attend and actively participate in team meetings.
• Help maintain a functional laboratory environment, including assisting with inventory, ordering, and overall lab cleanliness.
• All other duties as assigned.

Job Requirements

• B.S. degree in chemistry, pharmaceutical sciences, or a similar scientific field.
• 0-2 years’ experience in a CGMP pharmaceutical analytical laboratory.
• Strong CGMP documentation skills are required.
• Must be a detail-oriented person with strong analytical and communication skills.
• Ability to work in a fast-paced, entrepreneurial environment.

Benefits

Liquidia offers a competitive compensation package (base salary and commission) as well as a comprehensive benefits package that includes Medical, Dental, Vision, STD, LTD, 401(k) Savings Retirement Plan, ESPP, Unlimited Paid Time Off and more!

Liquidia is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform the essential functions of this position.

Recruiting Agencies, Please Note :

Liquidia will not accept unsolicited assistance from recruiting/search agencies for this employment opportunity. Please, no phone calls or emails. All resumes submitted by recruiting or search agencies to any employee at Liquidia via email, the Internet or in any form and/or method without a valid written search/recruitment agreement in place for this position will be deemed the sole property of Liquidia. No fee will be paid in the event the candidate is hired by Liquidia as a result of the referral or through other means.