Chemist I 2nd Shift

Quva; New Jersey; Sur place; USD 57 000 - 78 000; Plein temps

Avantages offerts par ce poste

Health and wellness benefits

401k with company match

17 paid days off + 8 holidays

Résumé du poste

Quva is seeking a Chemist I for the Bloomsbury, NJ site on a set 2nd shift schedule (Mon-Fri, 2:00 PM–10:30 PM). The role involves analytical testing of sterile products and raw materials, following cGMP/SOPs, with documentation and data reporting to ensure quality and safety. Ideal candidates hold a B.S./M.S.

in chemistry or biology and have 0–2 years of pharma lab experience. The position requires US work authorization and ability to lift up to 50 lbs.

Qualifications

• B.S. or M.S. in chemistry, biology or related field.
• 0–2 years of pharmaceutical lab experience.
• Must be authorized to work in the United States; Quva does not sponsor visas.

Responsabilités

• Conduct analytical testing of finished sterile products and raw materials per cGMP and SOPs.
• Provide analytical data in a timely manner.
• Draft testing protocols and reports for investigations.
• Keep accurate notebook records per cGDP requirements.

Connaissances

Analytical testing

Documentation

SOP understanding

Protocol drafting

Formation

B.S. or M.S. in chemistry/biology/related field

Description du poste

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 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.

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

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

• 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

Any Of The Following Will Give You An Edge

• B.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
• 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: $56,541 - $77,744 Annually + $5,200 / year shift differential

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.”

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