Description
Baxters BioScience division is a leading producer of both plasma-based and recombinant clotting factors for hemophilia, as well as biopharmaceuticals used to treat immune deficiencies, alpha 1 antitrypsin deficiency and other blood-related disorders.
* Baxter also produces vaccines for the prevention of infectious diseases, as well as biosurgery products used for hemostasis and tissue-sealing in surgery.
* BaxterResponsible for the general supervision of the center area training program.
* Is able to perform all technical tasks required within the work areas.
* Provides assistance to management to achieve business goals.
*Coordinates and performs new employee orientation, including company background, health and safety requirements, policies and procedures and other company expectations.
* Maintains complete and accurate records to ensure that all personnel are competent to perform their assigned duties.
*Works closely with the Facility Manager, QMR and management team to communicate center/employee needs as they relate to training.
* Ensures timely completion of cross-training and annual re-certification training.
* Reviews employee training materials to meet initial and annual certification requirements.
* Monitors center training needs and performs cross-training, re-training, SOP training, preventative action training and other training as needed.
* Ensures that employees are trained and committed to meet customer service expectations.
* Assures that all center employees comply with all federal, state, local and company-specific rules, regulations, and practices related to quality, to the safety of products, donors, and employees and to the proper performance of day-to-day activities.
*Understands Affirmative Action practices and is actively involved in employment application pre-screening and interviewing process for center staff.
*Fosters teamwork.
* Works collaboratively with staff, peers, and management to achieve business goals.
* Communicates continuously and resolves conflicts proactively.
*Effectively manages the production areas, motivates and encourages employees to meet their performance goals, and comply with company quality standards and procedures.
*Addresses donor and employee concerns in a timely manner.
*Maintains complete and accurate records, in accordance with cGMP.
*Other duties and responsibilities as assigned.
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Requirements
Ability to read and follow Standard Operating Procedures (SOPs) and to maintain complete and accurate records.
* Demonstrated work history of above average performance, customer service, and attendance.
* Must have effective oral and written communication skills.
* Demonstrated ability to organize and direct the work of others and resolve conflicts effectively.
*Associate or Bachelors degree preferred and or a minimum of one year relevant work experience, preferably in a regulated industry or an equivalent combination of education and experience.
*Percent Travel Required0%
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