Supervisor, Manufacturing - AID

Werfen•Norcross, GA

17h

About The Position

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We’re passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Position Summary: Inova Supervisors are responsible for overseeing the daily activities of their assigned team. This position is responsible for planning, scheduling and distributing work assignments for the manufacture of Inova products, while meeting productivity standards, quality goals, and department objectives. Responsible for resolving operational and performance issues and recommending improvements to operations, processes and the work environment. Works closely with direct reports and other departments daily. Communicates and collaborates with staff, department leadership, and other Inova staff to meet goals and produce the highest quality products and services. Ensures all staff are meeting Inova policies and administrative expectations. Activities are performed in accordance with standard operating procedures (SOPs), Quality Systems Regulations (QSRs), safety and administrative regulations.

Requirements

Bachelor’s degree in biology or related sciences required.
5+ years of experience in a regulated laboratory setting required; preferably in immunology or medical device manufacturing.
3+ years of experience leading or supervising a team required, within life sciences preferred.
Excellent knowledge of laboratory skills including solution preparation, bead-based assay manufacturing procedures and laboratory equipment operation.
Knowledge of Quality Systems Regulations (QSR) and Engineering Change Orders (ECO) systems as they apply to diagnostics manufacturing.
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Ability to deal with several abstract and concrete variables in defining problems, collecting data, establishing facts, and determining valid conclusions.
Experience with Enterprise Resource Planning (ERP) systems required, SAP strongly preferred.
Demonstrated experience with standard administrative and business procedures required.
Proven track record of organizing and supervising successful operations and teams required.
Ability to build consensus and relationships among peers, stakeholders and employees required.

Responsibilities

Supervises daily manufacturing activities carried out by the team/department, in compliance with Standard OperatingProcedures (SOPs), and other quality systems requirements, which may include, but is not limited to: Preparation of bulks and solutions Evaluation of raw materials, in-process materials, and finished reagents Development and compliance to master validation plans and ensuring applicable process and equipment validation protocols are developed, executed and maintained, as applicable. Maintenance and review of laboratory notebooks and and/or any associated documentation for manufacturing, evaluation and development activities. Research and correction of production issues. Set-up, calibration, validation, operation, cleaning and maintenance of laboratory equipment, as applicable. Creation, approval and implementation of Engineering Change Orders (ECOs) for manufacturing documents and SOPs.
Monitors operations to identify, evaluate and implement operational changes to improve performance, service, productivity, costs, etc.
Works with staff to assign tasks, answer questions, make decisions and resolve issues as they occur to ensure smooth daily operations.
Plans and monitors the flow of work into and through the team/department to ensure adequate materials and resources to meet productivity, quality and service expectations.
Trains and communicates with direct reports to ensure expectations are clear and staff comply with Quality Systems and administrative policies and guidelines.
Ensures all required documentation is completed, in accordance with Quality Systems Regulations (QSRs).
Investigates, analyzes and carries out corrective actions to maximize product performance or to resolve manufacturing problems, under the direction of department management.
Writes and revises SOPs.
Responsible for Engineering Change Orders (ECOs), for department documents, SOPs, Work Instructions and other Quality Systems documents.
Communicates and collaborates with other departments, people managers and staff to ensure smooth and efficient operations.
Assists with staffing decisions to ensure a high performing team; including interviewing, selecting, training and developing staff.
Manages department schedules to ensure department goals are achieved; responsible for approving schedules, time off, overtime, and timekeeping reporting.
Carries out performance management and development activities, including setting expectations, and providing meaningful feedback.
Provides opportunities for development, where possible. Proactively manages employee relations issues; uses judgement in consulting with department leadership and Human Resources.
Maintains regular and transparent communications throughout department through effective use of one-on-one meetings, team meetings and other forms of formal and informal communications.
Responsible for staff training, to ensure competency. Ensures staff compliance to training requirements.
Educates and supervises staff to ensure compliance with applicable Inova SOPs, ISO, FDA and other Quality System Regulations, as well as applicable Environmental, Health & Safety, Human Resources and all other regulatory and administrative policies.
Reflects the company values and serves as a role model to staff and customers.
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.