Senior QC Analyst

Croda International•Alabaster, AL

9d•Onsite

About The Position

Croda is a FTSE100 organization where we truly believe our people are our difference and this, along with our values of Innovative, Responsible and Together, creates ‘our Purpose, Smart science to improve lives™’. With over 5,000 employees globally, we specialize in the research and development of innovative ingredients for the Life Science and Consumer Care markets. We are focused on developing our inclusive culture through accountability, collaboration and innovation. By joining Croda, you will be part of a team who are using smart science to create a more sustainable future. As we deliver our ambitious 2030 Growth Strategy, we’re looking for a Senior QC Analyst, responsible for biological and chemical evaluation of raw materials, in-process, final release and stability samples ensuring compliance and timely completion of assigned task as well as other auxiliary laboratory support functions. May also serve as a subject matter expert in define areas and provide training and guidance to other analysts.

Requirements

Bachelor’s Degree in a scientific discipline
Laboratory experience of 4+ years required
Strong attention to detail
High level of integrity and reliability
Strong organizational and communication skills
Self-motivated
Ability to work in a team environment and independently
Proficient in Microsoft Office Suite

Nice To Haves

Relevant experience of 3+ years preferred

Responsibilities

Perform laboratory testing using standard laboratory procedures, principles, practices, concepts, and theories
Have a complete mastery of assigned SOPs and can train others in their execution
Develop and write SOPs as needed following GMP guidelines
Perform daily operation and routine maintenance, calibration, and assist in troubleshooting of laboratory instruments and equipment
Document and review routine data analysis, procedures, and results to ensure accuracy and compliance
Prepare and maintain standard operating procedures and prepare documentation for test verification or validation studies
Recognize basic problems and adhere to quality standard procedures
Assembles quality control data for further analysis; recognize problems; documents issues and initiates corrective actions
Consult and interact with external and internal partners regarding test methods and results
Responsible for preparation, calibration, and maintenance of laboratory and facility equipment
Assist with the procurement of supplies and materials
Perform duties associated with validation of QC assays
Promotes overall cleanliness/neatness of lab and storage areas
Communicates problems or potential issues in a timely manner
Maintain an understanding of cGMP and compliance in an analytical laboratory setting
Perform regular upkeep of employee training records and complete company required training programs
Prepare and align individual performance goals with department goals
Transfer strong knowledge of GMP guidelines/practices to new laboratory protocols and situations
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.