Shift Process Technician

Croda International•Alabaster, AL

4d•Onsite

About The Position

Croda is a FTSE 100 organization focused on developing innovative ingredients for the Life Science and Consumer Care markets. We are committed to fostering an inclusive culture through accountability, collaboration, and innovation. As we pursue our 2030 Growth Strategy, we are seeking a Shift Process Technician. This role is responsible for safely executing all operational aspects of production, including raw material charging, vessel operation, and performing procedures for bulk organic synthesis, biochemical processing, and purification of pharmaceutical products. All activities must comply with Safety, Health, and Environmental guidelines, government regulations, cGMP manufacturing, and process procedures.

Requirements

1 years’ 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 handle and complete multiple tasks simultaneously.
Ability to work both in a team environment and work independently.
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.

Nice To Haves

Bachelor of Science in chemistry, chemical engineering, biology or related field preferred.

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.
Effectively communicate with cross-functional teams including QC, R&D, QA and Management.