Supervisor, Manufacturing Operations (Compounding) 3rd Shift

Quva; Sugar Land (TX); On-site; USD 85,000 - 105,000; Full time

Benefits offered by this job

Full-time schedule

Health, dental, vision benefits

401k with company match

Paid time off (22 days) and 8 holidays

Job summary

Quva is seeking a Supervisor, Manufacturing Operations (Compounding) in Sugar Land, TX for a 3rd shift, 10:00 PM–6:30 AM. The role requires overseeing daily staffing and equipment in Compounding Operations with a strong focus on quality, safety, and adherence to cGMP and FDA requirements.

The position is safety-sensitive; candidates must be authorized to work in the United States and pass drug testing. Training and development opportunities are offered in a high-growth pharmaceutical environment.

Qualifications

• Minimum requirements include a high school diploma or GED.
• 2–3 years of prior experience in a cGMP / FDA regulated industry.
• 1 year of supervisory or management experience.
• Certified in-house qualification programs is a plus.
• Experience training personnel on aseptic techniques and gowning.
• Must be able to lift up to 50 lbs. throughout shift.
• Authorized to work in the United States; no Visa sponsorship.

Responsibilities

• Supervise staff in daily operations to meet production targets.
• Ensure operators follow validated parameters, SOPs, cGMP, and safety requirements.
• Counsel, train, and develop technicians for efficiency and teamwork.
• Complete in-process checks and verifications per SOPs.
• Review batch records and logs to ensure accurate documentation.
• Develop technician training programs and ensure operator training.
• Troubleshoot issues impacting daily/weekly deliverables and drive ownership.
• Review performance and drive opportunities for improvement.
• Support change control, CAPA, and GMP tasks to close on time.

Skills

Supervisory experience

Aseptic training

cGMP compliance

Problem solving

Attention to detail

Education

High school diploma or GED

Bachelor's Degree in Life Science

Tools

ERP software

Microsoft Office

Training software

Job description

Our Supervisor, Manufacturing Operations (Compounding) 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 Compounding 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.

This is a full-time role for our 3rd shift, working Monday through Friday from 10:00 PM to 6:30 AM. This is a set, consistent schedule based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What The Supervisor, Manufacturing Operations (Compounding) Does Each Day

• 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

Our Most Successful Supervisor, Manufacturing Operations (Compounding)

• 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

• 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
• Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
• 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

Any Of The Following Will Give You An Edge

• Bachelor’s Degree in Life Science or another related field
• Computer Skills
• Training Software
• Microsoft Suite
• ERP software

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
• 22 paid days off plus 8 paid holidays per year
• National, industry‑leading high growth company with future career advancement opportunities

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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