Shift Process Technician I

Croda International•Alabaster, AL

6d•Onsite

About The Position

Croda is a global organization specializing in innovative ingredients for the Life Science and Consumer Care markets. We are focused on developing an inclusive culture through accountability, collaboration, and innovation. As we deliver our ambitious 2030 Growth Strategy, we’re looking for a Shift Process Technician, responsible for safely performing all duties associated with the operational aspect of production, including but not limited to the charging of raw materials, the operation of vessels, executing the procedures and techniques associated with bulk organic synthesis, biochemical processing and purification of pharmaceutical products. All work is done with compliance with Safety, Health and Environmental guidelines, government regulations, cGMP manufacturing, and process procedures.

Requirements

Bachelor of Science in chemistry, chemical engineering, biology, or related field preferred.
1 year experience in pharmaceutical manufacturing in a preferred cGMP environment.
Strong attention to detail
High level of integrity and reliability
Working knowledge of Quality Management System in laboratory environment
Intermediate math skills
Intermediate mechanical skills required for manipulation of manufacturing equipment, such as glassware, glass reactors, pressure reactors, balances, Nutsche pressure filters, and gas cylinders.
Excellent written and verbal communication skills
Self-motivated
Proficient in basic applications such as Word, Excel, Outlook
Ability to manage and complete multiple tasks simultaneously
Ability to work both in a team environment and work independently

Responsibilities

Understand and follow established procedures to operate safely, in an environmentally sound manner, and according to cGMP including during emergencies, startup & shut down, and OSHA related issues.
Perform synthesis and purification of pharmaceutical products and fully document work
Access electronic communication and procedures regularly (e.g., email, Master Control)
Assist in troubleshooting, calibrating, and performing preventative maintenance on manufacturing equipment
Knowledge of personal protective equipment and use
Hold others accountable for safety and escalate issues as necessary
Perform inventory control of reagents and supplies
Complete drum movement training, and perform physical labor associated with movement
Maintain an elementary understanding of cGMP and compliance in a manufacturing setting.
Accurately and timely execute manufacturing SOPs/BPRs
Perform facility sanitation and maintenance
Sanitation of glassware, equipment, and fume hoods
Replace compressed gas cylinders
Complete respirator fitting and training
Perform label printing and verification
Perform upkeep of employee training records
Report and address any problems in daily manufacturing
Conduct laboratory duties in a cGMP/QMS environment
Perform as SME for QC/QA investigations
Transfer hazardous or nonhazardous waste materials to collection areas for disposal or recycling
Prepare and align individual performance goals with department goals
Complete company-required training programs
Adhere to all applicable regulations, policies, and procedures for health, safety, and environmental compliance as outlined in the company's Standard Operating Procedures, Chemical Hygiene Plan, Emergency Contingency Plan, training memoranda, policy memoranda, Safety Data Sheets, Specification Records, etc.
The job function routinely works with chemicals, organic solvents, and biological samples, and may on occasion require work with caustic chemicals.
Requires the ability to gown and wear safety attire as well as any required protective equipment including safety glasses.
Meeting hygiene and health requirements to comply with a cGMP environment.
Effectively communicate with cross-functional teams including QC, R&D, QA, and Management
Occasionally lift and/or moving items up to 50 pounds and manipulating drums (max. weight ∼ 650 pounds) using an appropriate drum handler.