What are the responsibilities and job description for the Associate Manufacturing Process Technician position at ApTask?
Night Shift 6:45PM - 6:45AM
C and D Rotation - Swing Shift - Week 1 is 5 working days Week 2 is 2 working days. Candidates must be available to work weekends.
Top 3 Must Have Skill Sets:
- Experience working in a team.
- Comfortable handling chemicals or can demonstrate the importance of lab safety.
- Can provide examples of troubleshooting (does not need to biotech or work related).
Ideal candidate: Systems MS office suite, Good written communication, experience working in a team not direct manufacturing experience understands the principles of safety culture and working effectively on a team, lab exposure and worked in an environment where safety is top priority. Manager is open to candidates that don't necessarily have experience in Biotech cross lateral could be anything with batch chemicals or chemical processing.
BASIC QUALIFICATIONS: Manager is requesting bachelors OR High school with 3 years work experience in manufacturing.
The Associate of Manufacturing will work in a dynamic production environment at the Drug Substance plant supporting commercial, clinical, and launch activities. Under general supervision, employee will perform operations in the Manufacturing area. Operations will be performed according to Standard Operating Procedures (SOPs).
Responsibilities include:
-Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment
-Weighing out buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
-Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
-Performing and monitoring critical processes with the ability to perform basic troubleshooting
-Performing in-process sampling of equipment and operating analytical equipment
-Performing parts washing and sterilization activities
-Maintaining an organized and clean workspace
-Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work
-Initiating and being involved quality deviation reports, as required
-Drafting and revising documents (SOPs, MPs)
-Identifying, recommending, and implementing improvements related to routine functions
