{"id":3323071,"url":"https://alion.io/job/onequva-chemist-i-2nd-shift","title":"Chemist I 2nd Shift","company":{"id":3832669,"name":"Onequva","domain":"onequva.com","url":"https://alion.io/company/onequva","size_band":"501-1000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"UltiPro","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Bloomsbury, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":56000,"max_usd":118000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":849},"experience_years_min":2,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false},{"name":"Machine Learning","optional":false}],"status":"live","first_seen_at":"2026-10-23T15:37:08Z","employer_posted_date":"2026-10-23","last_verified_at":"2026-10-28T03:29:40Z","board_verified":true,"closed_at":null,"days_open":4,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":4},"description":"Our Chemist 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 either validation studies for analytical methods, conduct stability analyses on drug products, or test of Raw Materials. You will execute testing per current test methods and follow all applicable SOPs and cGMP guidelines. 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.\nThis is a full-time role for our 2nd shift, working Monday through Friday from 2:00 PM - 10:30 PM. This is a set, consistent schedule based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.\nWatch this video to learn more.\nWhat the Chemist Does Each Day: \nConduct analytical testing of finished sterile products, and raw materials, following all written procedures and cGMP, and providing documentation of analyses\nProvide analytical data in a timely manner\nWork with the Supervisor to understand overall expectations and execute them independently based on the prioritization of projects\nReads and understands SOPs and follow policy, procedure, and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements\nDraft testing protocols and reports for investigations\nProvide input to R&D SOPs to enhance the efficiency of the laboratory\nKeep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements\nRecommend to Supervisor or Manager improvements to analytical test methods or to instrumentation\n Our Most Successful Chemists\nKeep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements\nComplete testing in a timely manner\nRecommend to Supervisor or Manager improvements to analytical test methods or to instrumentation\nMinimum Requirements for this Role:\nB.S. or M.S. degree in chemistry, biology or related field\n0- 2 years minimum laboratory experience in the Pharmaceutical Industry\nAble and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation\nMust be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas\nAny of the Following Will Give You an Edge:\nB.S. degree in chemistry, biology or related field with 2 + years laboratory experience in the Pharmaceutical Industry\nUnderstanding of cGMPs and Good Documentation Practice\nUnderstanding of various laboratory instrumentation\nBenefits of Working at Quva:\nSet, full-time, consistent work schedule\nComprehensive health and wellness benefits including medical, dental and vision\n401k retirement program with company match\n17 paid days off plus 8 paid holidays per year\nNational, industry-leading high growth company with future career advancement opportunities\nThe 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\nRange: $56,541 - $77,744 Annually + $5,200 / year shift differential\nAbout Quva:\nQuva 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.\nQuva 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. 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