Operations Manager

Grifols, S.A; Augusta (GA); On-site; USD 90,000 - 120,000; Full time

Job summary

Grifols, S.A is seeking an Operations Manager to lead donor center operations in Augusta, GA. You will supervise frontline staff, ensure compliance with FDA, OSHA, CLIA and cGMP standards, and drive production goals within approved budgets.

As acting Center Manager in their absence, you’ll coordinate training, quality control and donor recruitment efforts to maintain safety, efficiency and financial performance of the center.

Qualifications

• Direct leadership of frontline staff across donor floor operations.
• Ensures center activities meet SOPs and regulatory requirements.
• Oversees budget, production targets and quality goals.

Responsibilities

• Oversee donor center operations when Center Manager is absent.
• Coordinate with Training and Quality to meet goals.
• Manage schedules, personnel records and disciplinary actions.
• Develop action plans to maximize efficiency and profitability.
• Ensure donor recruitment campaigns and regulatory compliance.

Skills

Leadership

Operations management

Regulatory compliance

Budgeting

Staff development

Education

Bachelor's degree

Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

Summary

The Operations Manager is a key member of the donor center leadership team, responsible for overseeing day-to-day operational performance to ensure donor safety, regulatory compliance, and achievement of production goals. This role provides direct leadership to frontline staff across donor floor operations and ensures all center activities align with company standards, SOPs, and applicable regulatory requirements.

Assists with operational management of a Plasma Collection Center, ensuring compliance with all applicable policies and regulations and overall performance and profitability of the center. Acts on behalf of the Center Manager in his/her absence, may manage the center alone for days at a time. This position will manage employees in centers with over 50,000 liters.

Primary Responsibilities

• Responsible for all aspects of the donor center when the Center Manager is not present.
• Collaborates with Training and Quality staff to ensure that training and quality goals are met.
• Coaches and leads through effective feedback to employees through the Operations Supervisor(s).
• Monitors and evaluates operations. Works with the Center manager to develop action plans to maximize center efficiency and supervises the implementation of improvements. Makes critical decisions for the modifications of action plans.
• Responsible for all personnel functions including hiring, assignment and direction of work, development and training, disciplinary actions and termination and the maintenance of all personnel records
• Partners with the center manager in budget preparation and oversees facility to achieve production targets and quality goals at the agreed-upon cost structure.
• Actively delegates, monitors, and holds responsible the operations supervisors for their performance.
• Directs and supervises employees. This includes creating and managing work schedules.
• Establishes and maintains the ability to perform all tasks within the center; fulfills the role of production employees when the occasional need arises.

Other Responsibilities

• Assures center employees maintain the facility in a neat and clean condition and all equipment is kept in good working order.
• Responsible for freezer management, including overseeing plasma shipments and equipment failures. Required to answer all freezer alarms and deal with them appropriately
• Develops and implements active donor recruitment advertising campaigns to improve production levels.
• Maintains thorough familiarity and ensures compliance with state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedures, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice (cGMP).
• Directs key personnel in donor selection, plasma collection and all manufacturing records to maintain the highest production standards in accordance with state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedures, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), and Current Good Manufacturing Practice (cGMP).
• Builds rapport with donors to ensure overall customer satisfaction with the center to support long-term donation.
• Controls center donor funds and ensure that all financial records are accurate and in order.
• Keeps Center Manager informed of any irregularities within the center and provide action plans to improve and correct center deficiencies.
• Minimizes center liability through constant risk management review. Investigates all unsafe situations and Situations/complaints. Develops and implements required corrective actions.
• Directs and monitors the performance of outside vendors.
• Reviews and monitor special projects for accuracy and timely completion.
• Works with the Center Manager in implementing the donor center's mission into the community.

Education

Bachelor’s degree or equivalent, preferably in Science, Business, Nursing, Finance, or related field.

Experience

Typically requires 3+ years of related experience in clinical or general business experience. Supervisory experience preferred. Experience in a medical and/or cGMP regulated environment preferred. Experience with plasma or whole blood preferred.

Equivalency

Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor’s degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate’s degree with 6 years of experience, or a Master’s degree with 2 years of experience.

Knowledge | Skills | Abilities

• Developing command of leadership, organizational, customer service, interpersonal communication, and computer abilities. Ability to understand and assess FDA regulations.
• Ability to maintain adequate levels of plasma collection and adhere to quality standards.
• Ability to motivate staff to achieve established goals and standards.
• May be required to relocate

Occupational Demands Form # 6:

#BiomatUSA

Location: NORTH AMERICA : USA : GA-Augusta:

BTAGT - Augusta GA-Peach Orchard Rd-BPC

Learn more about Grifols (https://www.grifols.com/en/what-we-do)

Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.

Type: Regular Full-Time