Supervisor, Manufacturing Operations (Compounding) 3rd Shift

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