About this opportunity
QuVa Pharma lists this Microbiologist I 1st Shift opportunity in bloomsbury, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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 for our 1st shift, working Monday through Friday 7:30AM- 4:00PM. 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.
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What the Microbiologist I – Does Each Day:
Performs, compiles, and interprets results of microbiology tests including sterility, endotoxin, growth promotion, and microorganism identification.
Performs sterility testing utilizing a rapid technology
Successfully achieves and maintains gown qualification
Performs EM testing and daily, weekly, and monthly cleanings in support of daily operations in the Sterility Microbiology Cleanroom Suite
Executes endotoxin testing utilizing an end point fluorescence assay
Growth promotes incoming media and media fill samples
Documents the morphology of microorganisms and streaks isolates for identification
Performs grams staining, as needed
Our Most Successful Microbiologist I: Experience performing aseptic manipulations within a biological safety cabinet or laminar flow hood
Proficient with cGMP, 21 CFR Part 11, and electronic documentation systems
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
Seeks to identify continuous improvement opportunities
Minimum Requirements for this Role: Bachelor’s Degree required – Biology discipline preferred
0-2 years of experience in QC Microbiology
Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
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
Benefits of Working at QuVa: Comprehensive health and wellness benefits including medical, dental and vision
401k retirement program with company match
5 PLP and 12 PTO days off plus 8 paid holidays per year
National, industry-leading high growth company with future career advancement opportunities
The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions
Range: $49,164 - $67,600 per Year
About Quva:
Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma’s multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva’s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.
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.”
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.
Worksite address
bloomsbury, NJ, 08804, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.