Pharmaceutical Manufacturing Technician I - 2nd Shift
About The Position
The Manufacturing Technician I assists with manufacturing drug products, including parenteral or solid dosage products, for commercial distribution and clinical trials. The role supports operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory requirements and current Good Manufacturing Practices (cGMPs). The technician uses appropriate techniques and personal protective equipment (PPE), including gowning, and collaborates with other manufacturing areas as needed. This is a 100% on-site position, scheduled Monday through Friday from 3:00 p.m. to 11:30 p.m. The role may require occasional hours outside the scheduled shift, including weekend work, based on business needs, and up to 5% domestic travel.
Requirements
- High school diploma or GED.
- At least 1 year of GMP and prior pharmaceutical work experience.
- Excellent verbal and written communication and documentation skills.
- Strong attention to detail and organizational skills.
- Problem-solving and basic troubleshooting ability.
- Ability to perform basic math calculations.
- Ability to read and comprehend detailed written instructions.
- Ability to move materials throughout the facility using appropriate methods and equipment.
- Proficiency in basic computing skills.
- Ability to meet the physical demands of the role, including lifting and moving materials as described in the job posting.
Nice To Haves
- Associate’s degree.
- Awareness of or prior experience with cGMP practices and procedures.
Responsibilities
- Follow applicable SOPs and cGMPs when performing assigned duties and tasks.
- Complete company training requirements on time and in compliance with cGMP and other relevant requirements.
- Assist with manufacturing techniques, technologies, and equipment operation according to SOPs and cGMPs.
- Assist with operation of manufacturing and material-handling equipment.
- Document activities legibly and in real time on controlled documentation according to SOPs and cGMPs.
- Perform in-process testing, weight checks, component counting, and basic math calculations.
- Clean rooms, tools, and equipment.
- Support other manufacturing areas as required.
- Perform sterile-liquids manufacturing activities, including equipment and component preparation and sterilization, compounding, aseptic filling, and capping.
- Work occasional hours outside the scheduled shift, potentially including weekends, based on business needs.
- Perform other duties as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
