Chemist 1St 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 1st 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 analyses

• Provide analytical data in a timely manner

• Work with the Supervisor to understand overall expectations and execute them independently based on the prioritization of projects

• Reads 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

• Draft testing protocols and reports for investigations

• Provide input to R&D SOPs to enhance the efficiency of the laboratory

• Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements

• Recommend to Supervisor or Manager improvements to analytical test methods or to instrumentation

• Other duties as assigned

Our Most Successful Chemists

• Keep accurate notebook records in accordance with SOPs, cGMP and current Good Documentation Practices (cGDP) requirements

• Complete testing in a timely manner

• Recommend 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 country
• S. or M.S. degree in chemistry, biology or related field
• 0- 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 Industry

• Understanding of cGMPs and Good Documentation Practice

• Understanding of various laboratory instrumentation

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."