Quva
Supervisor, Manufacturing Operations (Formulation) 2nd shift
Quva, Bloomsbury, New Jersey, us, 08804
Supervisor, Manufacturing Operations (Formulation) 2nd shift
Apply for the
Supervisor, Manufacturing Operations (Formulation) 2nd shift
role at
Quva .
About This Role Our Supervisor, Manufacturing Operations (Formulation) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, you will be responsible for daily coordination and working schedules of people and equipment in Formulation Operations. 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.
Shift Details This is a full‑time role for our 2nd shift, working Monday through Friday from 2 PM to 10:30 PM. The schedule is set and consistent based on our site in Bloomsbury, NJ. This is a safety‑sensitive position that may be subject to random drug testing, in accordance with applicable laws.
Responsibilities
Runs operation to meet or exceed delivery performance objectives for product or projects
Supervises staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements; provides constructive operator feedback
Counsels, trains, & develops technicians for efficient performance; creates an atmosphere of team effort & open communication
Completes in-process checks & verifications in alignment with Standard Operating Procedures
Reviews documentation such as batch records and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation Practices
Develops technician training programs & assures operator training is conducted
Troubleshoots or resolves issues impeding daily/weekly deliverables; proactively demonstrates the ownership to achieve
Reviews operational performance and drives improvement opportunities
Initiates & executes change control assignments in support of continuous improvement initiatives for equipment, documentation, or processes
Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on‑time closure
Reports & initiates production schedule changes, requests equipment and facility repairs, or modifications
Ideal Candidate Traits
Meets productivity standards; Completes work in timely manner; Strives to increase productivity
Follows policies and procedures; completes administrative tasks correctly and on time
Prioritizes and plans work activities; Sets goals and objectives; Organizes or schedules other people and their tasks
Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments
Minimum Requirements
High school Diploma or GED from recognized institution or organization required
2-3 years prior experience in cGMP / FDA regulated industry
1 year of supervisory or management experience required
Successful completion of certified in‑house qualification programs
Experience training personnel on aseptic techniques and appropriate gowning techniques
Well versed in the compliance & quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolution
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
Additional Edge
Bachelor’s Degree in Life Science or another related field
Computer Skills
Training Software
Microsoft Suite
ERP software
Benefits
Set, full‑time, consistent work schedule
Comprehensive health and wellness benefits including medical, dental and vision
401k retirement program with company match
22 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: $65,023- $89,047 Annually
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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Supervisor, Manufacturing Operations (Formulation) 2nd shift
role at
Quva .
About This Role Our Supervisor, Manufacturing Operations (Formulation) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, you will be responsible for daily coordination and working schedules of people and equipment in Formulation Operations. 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.
Shift Details This is a full‑time role for our 2nd shift, working Monday through Friday from 2 PM to 10:30 PM. The schedule is set and consistent based on our site in Bloomsbury, NJ. This is a safety‑sensitive position that may be subject to random drug testing, in accordance with applicable laws.
Responsibilities
Runs operation to meet or exceed delivery performance objectives for product or projects
Supervises staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements; provides constructive operator feedback
Counsels, trains, & develops technicians for efficient performance; creates an atmosphere of team effort & open communication
Completes in-process checks & verifications in alignment with Standard Operating Procedures
Reviews documentation such as batch records and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation Practices
Develops technician training programs & assures operator training is conducted
Troubleshoots or resolves issues impeding daily/weekly deliverables; proactively demonstrates the ownership to achieve
Reviews operational performance and drives improvement opportunities
Initiates & executes change control assignments in support of continuous improvement initiatives for equipment, documentation, or processes
Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on‑time closure
Reports & initiates production schedule changes, requests equipment and facility repairs, or modifications
Ideal Candidate Traits
Meets productivity standards; Completes work in timely manner; Strives to increase productivity
Follows policies and procedures; completes administrative tasks correctly and on time
Prioritizes and plans work activities; Sets goals and objectives; Organizes or schedules other people and their tasks
Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments
Minimum Requirements
High school Diploma or GED from recognized institution or organization required
2-3 years prior experience in cGMP / FDA regulated industry
1 year of supervisory or management experience required
Successful completion of certified in‑house qualification programs
Experience training personnel on aseptic techniques and appropriate gowning techniques
Well versed in the compliance & quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolution
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
Additional Edge
Bachelor’s Degree in Life Science or another related field
Computer Skills
Training Software
Microsoft Suite
ERP software
Benefits
Set, full‑time, consistent work schedule
Comprehensive health and wellness benefits including medical, dental and vision
401k retirement program with company match
22 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: $65,023- $89,047 Annually
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.”
#J-18808-Ljbffr