Chemist 2nd Shift

Our Chemist 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.

This is a full-time role for our 2nd shift, working Monday through Friday. This is a set, consistent schedule based on site in our Bloomsbury, New Jersey location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What The Chemist Does Each Day

Conduct analytical testing of finished sterile products, and raw materials, following all written procedures and cGMP, and providing documentation of analysesProvide analytical data in a timely mannerWork with the Supervisor to understand overall expectations and execute them independently based on the prioritization of projectsReads and understands SOPs and follow policy, procedure, and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirementsDraft testing protocols and reports for investigationsProvide input to R&D SOPs to enhance the efficiency of the laboratoryKeep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirementsRecommend to Supervisor or Manager improvements to analytical test methods or to instrumentationOther duties as assigned

Our Most Successful Chemists

Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirementsComplete testing in a timely mannerRecommend to Supervisor or Manager improvements to analytical test methods or to instrumentation

Minimum Requirements For This Role

Legally authorized to work in the job posting countryS. or M.S. degree in chemistry, biology or related field0- 2 years minimum laboratory experience in the Pharmaceutical Industry

Any Of The Following Will Give You An Edge

S. degree in chemistry, biology or related field with 2 + years laboratory experience in the Pharmaceutical IndustryUnderstanding of cGMPs and Good Documentation PracticeUnderstanding of various laboratory instrumentation

Benefits Of Working At QuVa

Set, full-time, consistent work scheduleComprehensive health and wellness benefits including medical, dental and vision401k retirement program with company match17 paid days off plus 8 paid holidays per yearNational, 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.”