Fill/Finish Operator - (Manufacturing)

Work schedule is Monday to Friday 8am to 5pm, with the potential overtime/holiday hours, however, there will be shift changes in the future.

Will need to complete additional medical screenings

GENERAL PURPOSE: (A brief statement indicating the reason for the existence of this position)
This position is responsible for assisting with all aspects of aseptic / terminally sterilized / polymer (cleanrooms) and/or non-aseptic (Pilot Plant) processes and procedures for pharmaceutical and/or polymer manufacturing (development/engineering, clinical-phase and/or commercial).

PRINCIPAL ACCOUNTABILITIES: (The major activities or end results necessary to fulfill the position requirements on an ongoing basis)
· Demonstrate personal proficiency of aseptic technique with minimal supervision
· Accurately execute development/engineering, GLP or GMP batch records with direct supervision
· Accurately perform complex, multi-step solution preparations with direct supervision
· Assemble and disassemble process equipment on multiple unit operations for an extrusion, microsphere, liposome or polymerization process with direct supervision
· Operate PLC controlled equipment with direct supervision, including adjusting set-points as directed in batch records
· Use basic hand tools required for equipment operation
· Execute in-process environmental monitoring with direct supervision
· Participate in the execution of IOQs with direct supervision
· Perform other duties as required by supervisor
· Strict adherence to safety practices and procedures including use of personal protective equipment (PPE) appropriate for the type of hazard and exposure potential
· Actively participate in general area housekeeping
· Seek out and identify opportunities related to the maintenance, calibration, and improvement of company facilities, equipment, and procedures
· Perform responsibilities in compliance with the quality systems as described in ***s' Quality Manual
· Adhere to all company safety, health and environmental policies, procedures and directives
· Conduct all development/engineering, clinical=phase and/or commercial batches in a safe manner by use of MSDS to establish chemical hazards; observe the appropriate cGMP procedures; and report all incidents that could threaten the safety of company personnel

NATURE & SCOPE:
a. Qualifications – If you were transferred to a new position, list the specific education, skills, training, and relevant experience (in a similar or lower level position) that your replacement would need to qualify for this position.
· 0-2 years relevant industry experience as determined by management
· Basic computer skills
· Basic math skills including addition, subtraction, multiplication, and division. Ability to perform calculations when supplied with the equation.
· Ability to read and follow detailed written instructions
· Thorough understanding of all general lab glassware
· Basic understanding of system controls and data logging software

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.