Manager, Manufacturing Operations (Compounding) 2nd Shift

Our Manager, Manufacturing Operations plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include managing the manufacturing of sterile pharmaceuticals within the facility. The primary function is to oversee all operations, and personnel, of Inspection, Labeling and Packaging Operations where multiple requirements and challenges will exist requiring a good knowledge base and ability to apply operational, quality, and regulatory skill sets. 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 2:00pm to 10:30pm 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 Manager, Manufacturing Operations Does Each Day:

Manages staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements

Runs operation to meet or exceed delivery performance objectives for product or projects

Counsels, trains, & develops Supervisors for efficient performance; creates an atmosphere of team effort & open communication

Prepares and submits weekly/monthly reports, prepares metrics and trends data to identify and prioritize continuous improvement opportunities

Establishes & maintains cooperative cross-functional relationships with peers in Quality, and other manufacturing operations colleagues to meet plant objectives

Leads in development & maintenance of a safe manufacturing environment. Participates in safety meetings, investigates accidents, and takes appropriate corrective action to eliminate hazardous conditions

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

Our Most Successful Manager, Manufacturing Operations:

Has Strong technical writing and verbal/written communication skills, including presentation skills

Has excellent interpersonal skills demonstrating the ability to interact with people holding positions in many different departments

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 for this Role:

Bachelor’s Degree in Life Science or another related field

5 years of supervisory or management experience

Hands-on direct shop floor involvement: Troubleshooting

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:

3 years prior experience in cGMP / FDA regulated industry

Understanding of process flows, gap assessments and analysis of data to drive improvement

Proficiency with computerized tracking tools

Comprehensive knowledge of adult learning techniques

Benefits of Working at Quva:

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

Occasional weekend and overtime opportunities with advance notice

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: $98,891-$135,975 + $5,200 shift differential

This role is also eligible for an annual incentive bonus, subject to program terms and guidelines

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.