Microbiologist I

Our Microbiologist I plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete training, you will be required to perform individual hands-on work in the sterility testing and/or endotoxin testing programs. This person provides scientific guidance and interpretation of microbiology results to QC and production management. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a full-time role, working Monday through Friday. This is a set, consistent schedule based on site in our Bloomsbury location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What the Microbiologist I – Does Each Day:

Performs, compiles, and interprets results of sterility and/or endotoxin tests

• Performs the Microbiology Laboratory daily, weekly, and monthly cleanings in the Sterility Microbiology Lab
• Successfully achieves and maintains gown qualification
• Performs tests to detect harmful microorganisms and obtains information in contamination or other scientific measures
• Documents and examines physiological, morphological growth structure, and other additional characteristics to identify and classify microorganisms

Our Most Successful Microbiologist I:

• Plans, schedules, prioritizes, and manages time to meet project goals of regulatory compliance and facility requirements
• Makes decisions, set priorities, and schedule work for self
• Interacts with management and co-workers in a calm, courteous and professional manner
• Observes and constructively trains and corrects laboratory and production staff, as well as collaborate with management to resolve issues in a timely manner

Minimum Requirements for this Role:

• Must be currently authorized to work in the United States on a full-time basis; QuVa is not able to sponsor applicants for work visas

• Bachelor’s Degree required – Microbiology discipline preferred
• 0-2 years of experience in QC Microbiology

Any of the Following Will Give You an Edge:

• Understand FDA and 21CFR Part 211 cGMP requirements and guidelines for sterile drug products
• Proficient in proper Aseptic Techniques and Growing procedures
• Experience in a pharmaceutical manufacturing environment
• Strong Microsoft Word and Excel skills

Benefits of Working at QuVa:

• Set, full-time, consistent work schedule
• Comprehensive health and wellness benefits including medical, dental and vision
• 401k retirement program with company match
• 17 paid days off plus 8 paid holidays per year
• National, industry-leading high growth company with future career advancement opportunities

About QuVa:

QuVa Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.

As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.

QuVa is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. QuVa's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with QuVa is “at will.”