Supervisor, Manufacturing Operations (ILP) 1st Shift

Our Supervisor, Manufacturing Operations (ILP) 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 Inspection, Labeling and Packaging Operations and Label Printing Operations (as applicable). 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 1st shift, working Monday through Friday from 6:00 AM - 2:30 PM. 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 (ILP) Does Each Day:

Supervises staff in execution of daily work; assures production technicians comply with standard operating procedures, cGMP regulations and safety requirements; provides constructive operator feedback
Supervise label printing activities as needed
Supervises ILP schedule in accordance with production schedule and customer demand
Prepares and submits daily/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; Establishes methods in compliance with regulatory, plant, and corporate policies
Participates in safety meetings, investigates accidents, and takes appropriate corrective action to eliminate hazardous conditions
Oversee production activities to assure performance to plan is achieved
Recognizes and sets priorities and takes prompt action
Forecasts and sets goals and objectives, identifies and allocates resources as needed
Effectively identifies gaps in strategy and resources and resolves them
Effectively arranges for work to be completed, schedules workflow and assignments to ensure delivery performance objectives for product or projects are met or exceeded
Manages front line leadership in completion of daily operational tasks and assignments
Counsels, trains, & develops front line leaders for efficient performance and assists in their career development; creates an atmosphere of team effort & open communication
Supports regulatory inspections such as DEA and FDA audits
Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on-time closure
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 training programs & assures training is conducted
Reports & initiates production schedule changes, requests equipment and facility repairs, or modifications

Our Most Successful Supervisor, Manufacturing Operations (ILP) has:

Strong technical writing and verbal/written communication ability, including presentation skills
Interpersonal skills demonstrating the ability to interact with people holding positions in manufacturing, both operations and quality including compounders, pharmacist, supervisors, area management, quality specialist as well as functional areas such as Human Resources, IT, Customer Service, Finance and Pharmacy Services
Development of action plans to meet a specific objective including identification and methods of tasks, milestones, resources requirements and metrics
Successful time management skills to coordinate successful accomplishment of an approved action plan with timelines and milestone tasks
Understanding of process flows, gap assessments and analysis of data to drive improvement
Proficiency with computerized tracking tools
Comprehensive knowledge of Adult learning techniques

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

- Well versed in the compliance & quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolution

- Will be required to undergo a color perception exam and must be able to produce a passing test result

- Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction

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

- 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:

- Bachelors Degree in Life Science or other related field

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

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

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 Pharmas 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. Quvas 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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