Quva Pharma Sugar Land , TX 77487
Posted 4 weeks ago
Our Lead Inspection, Labeling and Packaging (ILP) Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. The role oversees planning, scheduling, staffing and daily execution for the inspection, labeling and packaging of compounded sterile products (CSPs), bulk bags and non-sterile solutions. Your attention to detail and adherence to precise procedures will guarantee that our medications reach patients accurately and securely. 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 with minimum overtime requirements and based on site in our XXXX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.
Watch this video to watch more
What the Lead ILP Technician Does Each Day:
Oversees inspection, labeling and packaging operations, including scheduling, processing, and completion of finishing activities in support of CSPs, bulk bags and non-sterile solutions
Serve as a knowledgeable resource for any team member who needs assistance with products or procedures as well as SME for cross functional project teams
Works with label printing teams to ensure appropriate inventory of labels is maintained to support production, including escalation as needed to meet production targets
Supports development of weekly ILP plans and schedules
Ensures timely communication and coordination of activities to ensure materials are transported and processed in accordance with internal procedures to meet established timelines for delivery and internal processing
Resolves and escalates non-routine incidents immediately
Ensures proper cleaning of the processing rooms in accordance with procedures
Conducts initial and on-going training of new operators, demonstrates proper techniques, provides coaching, tracks development, completes required documentation, and advises management of progress; regularly attends training meetings
Ensures the proper operation of process equipment in accordance with internal policy and procedure
Escalates to supervision information related to individual who call in or arrive late to line
Our Most Successful Lead ILP Technicians:
Understand and adhere to all company policies and procedures
Recognize priorities and take appropriate follow-up action
Have strong written and verbal communication skills
Successfully interact with co-workers on various teams and at various levels to achieve desired outcomes
Continually strive to improve efficiency without compromising quality
Create / revise training plans to meet a specific objective, including milestones, consideration of resources
Have good decision-making skills
Minimum Requirements for this Role:
High school Diploma or GED from recognized institution or organization
At least 1-year pharmaceutical manufacturing experience or labeling and/or packaging experience
Must be currently authorized to work in the United States on a full-time basis; QuVa will not sponsor applicants for work visas
Any of the Following Will Give You an Edge:
BA degree
Proficient with MS Office inclusive of Word, Excel and PowerPoint
Familiarity with basic operation of ERP systems
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
17 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
About QuVa:
QuVa Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.
As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.
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."
Quva Pharma