Shift Process Technician I
Job
Croda International Plc
[Unknown City], AL (In Person)
Full-Time
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Job Description
Shift Process Technician I Shift Process Technician Croda is a FTSE100 organization driven around our purpose of Smart Science to Improve Lives™. With over 6,000 employees across 39 countries, we are focused on the research and development of novel and highly sustainable raw materials for the Life Sciences and Consumer Care sectors. We are passionate and excited about how we can develop and utilize new technologies to shape and inspire changes within an ever-growing marketplace. As our business looks to deliver its ambitious strategy of growth, we are looking for a Shift Process Technician to join our Manufacturing Team . You will be 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 done with compliance to Safety, Health and Environmental guidelines, government regulations, cGMP manufacturing and process procedures.
What You'll Be Doing:
Be part of a team that values diversity, sustainability, and continuous innovation, where your ideas and contributions matter.- 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 trouble-shooting, 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.
Who We're Looking For:
At Croda, we believe our people are the heart of our success. We are committed to fostering an environment where you can grow, make a meaningful impact, and thrive.- Bachelor of Science or equivalent unless previous employment experience indicates aptitude. Bachelor of Science in chemistry, chemical engineering, biology or related field preferred.
- 1 years' experience in pharmaceutical manufacturing in a cGMP environment preferred.
- 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 Don't meet all the qualifications?
What We Offer:
Join a global organization with countless opportunities for growth and leadership. The successful candidate will receive a competitive salary and benefits package including:- Excellent Medical, Dental, and Vision coverage, available immediately.
- Generous PTO
- 401K Match
- Wellness Reimbursement
- Parental Leave
- Career Development
- Company paid and voluntary Life and AD&D Insurance
- Short and long term disability
- Paid Holidays And more!
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