Center Manager

KEDPLASMA provides a friendly and rewarding working environment with frequent opportunities for cross-training and advancement.

Please apply if you meet any of the criteria described below, with relation to the job duties and responsibilities. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran Biopharma & KEDPLASMA offer a number of benefits to qualifying employees, including :

• Medical, vision and dental insurance
• Life and AD&D insurance
• Paid holidays
• PTO accrual
• and much more!If you would like further details regarding the benefits we offer please let us know, and we would be glad to provide you with our full benefits guide, as well as answering any questions you may have!

JOB SPECIFICATIONS :

Bachelor's degree in science or management related field required. Previous work

experience demonstrating decision making ability, ability to effectively communicate with

and positively influence people, familiarity with fiscal operations, supervisory

responsibility, conflict resolution, and customer service.

• Excellent communication skills and ability to conduct oral presentations.
• Excellent people skills which extends to a diverse group of individuals and demographics.
• Three to five years of working experience in a biomedical field preferred or a combination

of advanced education and related experience.

• Ability to speak, read and write in English. Professional appearance and demeanor.
• Ability to operate computer software including DMS (with training) and Microsoft Office.

PHYSICAL REQUIREMENTS :

• Ability to sit or stand for up to four (4) hours at a time.
• Ability to tug, lift, and pull up to fifty (50) pounds.
• Be able to bend, stoop or kneel and climb stairs and / or ladder.
• Occupational exposure to blood-borne pathogens.
• Able to travel by plane and drive car.
• While performing the duties of this job, the employee is regularly required to stand; use

hands to handle or feel objects, tools or controls.

Duties and Responsibilities :

• Maintains Regulatory Compliance
• Ensures the compliance of all Center activities with Kedplasma DCOP's (Donor Center

Operating Procedures) and other Company standards and protocols to meet the

regulatory requirements of the FDA, EMEA, Customer Specifications, and other regulatory

bodies as required.

• Includes training in all operational areas,
• Ensures proper equipment maintenance, calibration and cleaning schedules as required.
• Maintains freezer and refrigerators within required temperature ranges and maintenance

requirements. Manages freezer temperature alerts as necessary.

• Ensures the facility is well-maintained, safe, clean, and neat at all times.
• Maintains a thorough understanding of State and Federal regulations (e.g., FDA approved

Standard Operating Procedures, OSHA, CLIA, IQPP Standards and cGMPs) to maintain

the highest production standards and ensure facility compliance.

Reviews test results to ensure that abnormal and reactive test results include prompt unit

culling and quarantine, computer entry, execution of lookbacks and final disposition of

product.

Quality Assurance review as needed regarding E&A (Error and Accident) and CAPA follow

up and resolution.

• Holds regular meetings with QAM for revisions and updates to training
• Develops an understanding of NAT testing protocols and maintains IQPP Viral Marker

Standards.

• Problem Resolution
• Maintains all aspects of daily center functions (e.g., personnel, products, donors,

computers, etc.).

Keeps immediate supervisor informed of any irregularities within the center and provides

constructive information about process improvements.

Minimizes center liability through constant risk management review; including review of

Medical Incident Reports, minor incident logs, and drives effective, timely corrective

actions.

Manages all donor incidences including donor red cell loss, over / under draws, donor

reactions and behavioral issues.

• Directs donor recruitment techniques and manages customer and donor complaints.
• Inventory and Sample Management
• Ensures that product shipments and sample submissions are accurate and performed in

accordance with shipping schedules.

Ensures that center is in compliance with directives on shipping listed in the DCOP and

instructions provided by the corporate logistics group.

• Ensures FDA licensed product; SISPQ (strength, identity, safety, purity and quality).
• Manages product inventory within the Center with assistance of Logistics.* Responsible for Supervision, Training and Development of Staff
• Trains, develops, and manages all staff in accordance with the Employee Handbook and

Policy Manual, DCOP's, Training Manual and other established management guidelines

and regulations.

• Hires, motivates, and evaluates center personnel based on established guidelines.
• Disciplines and terminates center employees and maintains complete, accurate

personnel records.

Ensures adequate, trained staff is available to cover the hours of operation in adherence

to regulatory requirements.

Creates an organizational environment that stimulates the morale and productivity of the

work force and its leadership.

• Budget and Fiscal Control
• Maintains a professional and courteous relationship with donors that will stimulate donor

retention, referrals, and production growth.

Ensures projected production budget is met in quantity, quality and within required titer

requirements.

Along with VP of Operations and / or Regional Manager, manages the Center as cost

effectively as possible without sacrificing quality, to include employee time management