Supervisor, Manufacturing Operations (Compounding) 3rd Shift

QuVa - Advancing Healthcare Possibilities; Sugar Land (TX); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Health and dental benefits

401k with company match

22 paid days off + 8 holidays

Career advancement opportunities

Job summary

Quva is seeking a Supervisor, Manufacturing Operations (Compounding) in Sugar Land, TX, for a 3rd shift role from 10:00 PM to 6:30 AM. The position upholds strict cGMP and safety standards within our compounding operations.

You will coordinate daily schedules, supervise staff, and ensure adherence to validated parameters. The role requires strong attention to detail and a commitment to quality in serving patients across the US.

Qualifications

• High school diploma or GED required.
• 2–3 years in a cGMP/FDA regulated industry.
• 1 year of supervisory or management experience required.
• Certified in-house qualification programs completed.
• Experience training personnel on aseptic techniques and gowning.
• Able to walk, stand and lift up to 50 lbs.
• CGMP compliance knowledge beneficial.

Responsibilities

• Runs operation to meet or exceed delivery objectives.
• Supervises staff and ensures SOPs, cGMP and safety requirements are followed.
• Counsels, trains, and develops technicians for performance.
• Performs in-process checks and verifications per SOPs.
• Reviews batch records and logs for compliance and documentation quality.
• Develops technician training programs and ensures training completion.
• Drives continuous improvement initiatives and change control.

Skills

Supervisory experience

cGMP knowledge

Team coordination

Problem solving

Attention to detail

Education

HS Diploma or GED

Bachelor's Degree (Life Sciences or related)

Tools

ERP software

Microsoft Office

Training Software

Job description

Job Category: 7000-Operations Support

Requisition Number: SUPER006175

• Posted : October 26, 2026
• Full-Time
• On-site

Locations

Showing 1 location

TX - Sugar Land 1075
1075 W Park One Dr #100
Sugar Land, TX 77478, USA

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
• 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:

• 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 BrightStreampartners 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.”

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.