Pharmaceutical Assistant

Responsibilities

• Operate Dabrico's, labelers, canning, casers, overwraps, checkweighers, cartoners and other machinery per assigned room.
• Ensure product quality during the production process.
• Perform line clearances and verify filter MIT's.
• Pull and deliver QC samples.
• Check in cages and warehouse materials.
• Perform pH testing (in-process) for fill lines and volume testing/leak tests.
• Prepare documentation of sterilization and daily tags.
• Notify Group Leader/Supervisor of all safety issues.
• Maintain proper documentation - batch records, check sheets, logbooks.
• Ensure preventative maintenance is current.
• Perform all tasks in a safe manner and stay current with training requirements.
• Perform room and equipment sanitation.
• Equipment/machine cleaning and basic sanitation.
• Ensure adherence to all plant safety rules in area of responsibility.

Requirements

• High school diploma or equivalent (GED)
• 0-1 years experience working in a manufacturing and/or industrial type environment
• Able to make minor mechanical machine adjustments.
• Must be self-motivated, with a problem-solving mindset.
• Ability to work effectively both independently and as a part of a team.
• When assigned to a fill line must be aseptically trained.
• Must be able to communicate and work well interdepartmentally, as well as, with all plant departments.
• Must be able to read and write, as well as follow written and oral instructions.
• PHYSICAL/MENTAL REQUIREMENTS
• Required to do frequent lifting of 15-20 pounds and occasional lifting in excess of 25 pounds.
• Vision must be correctable to 20/20.
• Must be able to withstand exposure to inks, solvents and liquids.
• Stand for up to 8 to 12 hours depending on assigned area.
• Must be able to push, pull and/or lift above shoulders.
• Push and pull heavy carts or tanks.
• NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
• Standard A/B schedule.
• 6pm-6am
• Ability to work overtime as needed.
• Work Location Assignment: On Premise
• Relocation assistance may be available based on business needs and/or eligibility.
• Candidates must be authorized to be employed in the U.S. by any employer.
• U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
• Sunshine Act
• EEO & Employment Eligibility
• Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national orig

Benefits

Additional Information

ROLE SUMMARY Performs light inspection and/or a limited number of manual and/or automated manufacturing support functions. Performs verification of defects for development of defect kits. This may include line clearance, outfeed/accumulation, scale operation, overwrap, carton/casing, canning, labeling, capping stoppering, and equipment/machine cleaning and sanitation in compliance with SOPs, cGMPs, batch records, TCPs, BOMs and POPs.

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