Chemist I 1st Shift

Quva • Bloomsbury, NJ

2d • Onsite

About The Position

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. This is a full-time role for our 1st shift, working Monday through Friday from 6AM to 2:30PM. 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. Watch this video to learn more.

Requirements

• B.S. or M.S. degree in chemistry, biology or related field
• 0- 2 years minimum laboratory experience in the Pharmaceutical Industry
• 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

Nice To Haves

• 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

Responsibilities

• 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
• 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

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level