- Operator I Functions
- Adherence to safety and quality procedures
- Product quality, throughput and final yields
- Excellent attendance, punctuality, and dependability
- Operators' work ethic and general attitude as it pertains to the daily operations of the facility
- Must be dependable, ready/eager to learn and able to meet the physical requirements of the job.
- Prior manufacturing experience and work in a regulated environment preferred.
- Ability to work weekday and weekend OT a plus.
- Communication Skills Oral and Written
- Basic Math Skills, interpretation
- Potential limited exposure to heath & physically hazardous chemicals.
- Personal protective equipment, including gloves, a respirator hood, safety glasses, safety shoes and other Personal Protective Equipment is provided and is required to be worn in designated areas.
- Prior Production Experience preferred
- Physical strength, stamina and dexterity while wearing fully enclosed air suite
- Employees be able to lift or move items up to 44 lbs. (20kg) individually, or with a two-person lift between 45 lbs and 76 lbs. (35kg). 77 lbs and over with a lift assistance device.
- Ability to work safely with high potency active pharmaceutical ingredients (HPAPI) as well as novel compounds of unknown potency and toxicity
- Ability to stand or walk for up to 8 hours per day.
- Ability to climb steps/ladders and occasionally work from elevated platforms.
- Ability to wear a respirator hood and pass the required respiratory medical exam.
- Ability to work in loud environments and wear various types of hearing protection
- Ability to work with chemicals, health/physical hazardous material safely and in compliance with the site safety program
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Machine Operator - Malvern - Pharma Resource Group
6 days ago
Description
The Process Operator micronize mills client provided material including both active pharmaceuticalingredients and excipients as per Client's Malvern procedures and policies, client instructions
and cGMP guidelines. Consistently models Client's values and leadership behaviors in all interactions.
o Set up, operate equipment, and monitor production processes.
o Report production on batch records following good documentation procedures (GDPs).
o Work in a regulated environment with adherence to standard operating procedures and policies.
o Adhere to cGMP standards.
o Identify and communicate non-routine events, deviations, and GMP deficiencies to supervisor promptly.
o Clean the entire processing area and processing equipment.
o Produce thorough, clear, and consistent documentation in compliance with Quality Standards (Attributable, Legible, Contemporaneous, Original, and Accurate).
o Demonstrate willingness to accept change, learn, and work with new processes.
o Stop and ask questions or suggest improvements when something is unclear.
o Participate in shift change meetings, site/team meetings, sending/receiving emails, offering suggestions for improvements, and participating in projects.
o This is a site-based position.
o Strive to achieve First Time Right (FTR) as a key performance indicator (KPI) in order to meet our yearly targets.
Measures of Performance:
III
Position Requirements:
Education or Equivalent:
High School Diploma or GED
Experience:
Knowledge/Skills Requirements:
Technical Skills/Knowledge
Physical Requirements/Work Environment:
Ability to perform moderate physical labor including:
lifting, climbing, bending,
crouching, reaching and twisting
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