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.

SHIFT: 1st

HOURS: 7am-3:30pm, Monday-Friday

Summary-

The Technician I is an entry level Aseptic Fill technician role that performs fundamental tasks within a GMP environment by cleaning and maintaining the workplace. The Technician I will routinely disassemble, clean, and reassemble equipment for production activities, assist with process control manipulations, use various computer control systems and analytical equipment. Perform real time documentation in appropriate production procedures while maintaining accurate records and logs.

Tech I:

Responsibilities:

Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals

Class A/B gowning qualified for facility cleaning of fill suites

Operate support fill equipment such as the glass inspection stations, rinser/tunnel, VAM and over sealer. Load carts with vials or syringes

Perform SIP Operations and filter integrity testing

Prepare chemical solution for production use. Strict adherence to Dept. Safety Rules.

Perform material handling and glass inspection activities

Detailed, general facility housekeeping i.e. minor cleaning, keeping work and production area neat and free from clutter, etc.

Cleaning - Sanitization per procedures, documentation of sanitization, mopping, disinfecting (floors, walls, equipment)

Operate motorized (ie Fork truck, lift jack, etc.) transport equipment for moving supplies

Real time documentation (i.e. BPR) during production run and maintain accurate records/logs

Monitor and operate various computer control systems for production activities i.e. SCADA and Andover

Summary-

The Technician II independently performs fundamental tasks within a GMP environment by cleaning and maintaining the workplace. The Technician II will independently dissemble, clean, and reassemble equipment for production activities, perform process control manipulations, use various computer control systems and analytical equipment to perform real time documentation in appropriate production procedures while maintaining accurate records and logs. The Technician II will be expected to recognize and identify safety hazards, perform basic training to less experienced personnel, and utilize troubleshooting skills in alignment with job responsibilities.

Tech II

Responsibilities

Prepares and properly labels according to BPR and non-routine request

Independently interprets and utilizes information from company support systems

Maintaining all training responsibilities associated with the Technician II level

May operate and monitor final container lyophilization, heat treatment, pasteurization and cold box.

Operate and filer integrity tester and gas chromatography for lexsol detection

Demonstrates department specific aseptic techniques and capabilities

Performs all duties described at the Aseptic Filling Level

Accurate documentation skills. Basic computer skills. Mechanical aptitude. Ability to work well with others in a team environment. Self-starter with the ability to work independently and use good judgement. Able to handle multiple priorities. Proactive, results oriented, and strong attention to detail.

Maintain acceptable aseptic gowning qualification and media fill certification.

Setup and operate equipment within an aseptic environment

Utilize troubleshooting skills in alignment with job scope responsibilities to provide solutions

Assist with initial responsibilities for the Technician level. Trains less experienced Technicians in the use of applicable computer systems.

Knowledge, skills abilities:

Must possess a good math and mechanical aptitude with the ability to perform skills in an aseptic environment. Production work experience in a high-volume manufacturing environment is desired. Must be able to function in an aseptic environment while maintaining the sterility of the product. Able to work effectively and efficiently as a member of a team. Able to lift up to 50 pounds. Continuous standing, walking and some bending is required. Off shift and overtime work may be necessary.

Requirements:

High School Diploma. Bioworks Certification preferred.Work is performed in a manufacturing environment with rotating shifts. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to chemicals and to electrical manufacturing equipment and moving machinery. Exposure to high levels of noise. Occasional entry into confined spaces, requiring kneeling and squatting. Personal protective equipment required such as; protective eyewear, chemical suits, safety shoes and/or rubber footwear, gloves, hearing protection and a respirator. Work is performed sitting for 4-6 hours per day. Occasionally walks, stands and bends waist for 2-4 hours per day. Frequent hand movement of one hand with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Light to moderate lifting and carrying of 15-44lbs. for 1-2 hours per day with a maximum lift of 50lbs. May reach above and below shoulder height. Hearing acuity essential. Color perception/discrimination, far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Frequently performs simple and routine tasks that vary little each day by following a set of written or oral instructions/procedures.

Third Party Agency and Recruiter Notice:

Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.

Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law. We will consider for employment all qualified Applicants in a manner consistent with the requirements of applicable state and local laws.

Learn more about Grifols

Req ID: 521020

Type: Regular Full-Time

Job Category: Manufacturing