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Production Chemist II role for a Medical Device Company. Duration: 12+ Months Contract. Total Hours/week: 40.00(Mon-Fri). 1st Shift. Standard 8-hr shift; 8-5 pm (including lunch), Onsite.
Job Responsibility:
Support the production of commercial dyes using established technical SOPs
Perform variety of chemical reactions and subsequent processing, purification, and characterization steps
Support inventory management of raw materials, intermediate products, finished goods, analytical samples, and QA Retains through cycle counts, database management, etc.
Work collaboratively with Research, Sustaining Engineering, Process Development, Quality Control, Quality Assurance, and other Production Chemists/Supervisor to ensure successful transfer of new products into Production and to improve processes within the production department
Documentation in lab notebooks, batch records, and basic databases
Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices
Other responsibilities or projects as assigned by reporting manager
Requirements:
M.S. degree in Chemistry with a minimum of 2 years of experience in an industry synthetic chemistry lab or a B.S. in Chemistry with 3+ years of relevant work experience
Industry laboratory experience (prefer chemistry over biochemistry/bio)
Experience working in an ISO, GMP, or GLP environment
Organization skills
Solid MS Office Knowledge, Intermediate to Advanced Excel usage
Ability to follow standard operating procedures
Must possess strong organizational skills, attention to detail, and the ability to adapt to changing priorities in a fast-paced environment
Be a self-starter, quick learner with the ability to work independently and efficiently
Hands-on team player with the ability to be proactive and work independently
Ability to influence others without direct reporting ties
Strong ability to focus and work efficiently inside of a project-oriented team
Strong diagnostic, analytical and technical ability
Demonstrated systematic problem solving
Nice to have:
Experience with rotary evaporation and working in a glovebox
Experience working in an ISO or QMS environment and with CAPA investigations
Strong interpersonal communication skills, effective written and oral communications skills