NJ Labs
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Overview
The Chemist Level 1 position must be able to understand, comply, and be familiarized with company policies. Chemist 1 must comply with CGMP, GLP, GDP and NJL safety policies. They must follow respective standard operation procedures and quality practices established by the Quality Assurance and Regulatory Affairs Departments. The position requires basic knowledge of chemistry and mathematics to solve problems and support analyses and techniques used in the laboratory. Responsibilities
Perform and document routine work assigned, including operating analytical instruments and performing wet chemistry analysis in compliance with standard operating procedures, compendial monographs, policies, and regulations. Abide by ALOCA principles (Attributable, legible, contemporaneous, original and accurate). Follow CGMP/GLP laboratory practices and documentation relevant to duties; comply with company requirements and regulations. Record and document observations and procedures in laboratory notebooks in accordance with GMP. Calibrate basic instruments as needed (e.g., analytical balances, pH meter). Operate trained and assigned common laboratory equipment and perform wet chemistry analyses. Prioritize tasks and manage workload to meet business needs and deadlines, including urgent, rush, and standard turnaround times. Maintain instruments and equipment as required/needed. Ensure testing and results are conducted and reported without compromising quality and released in a timely manner. Prepare test solutions and standardize volumetric solutions as needed. Ensure supplies and reagents are in stock; segregate expired chemicals; communicate with managers and QC Coordinator. Follow proper waste disposal and environmental regulations; maintain a safe, clean, and organized laboratory environment. Ensure fume hoods are maintained after use. Notify QC Manager, Technical Supervisor, or Quality Assurance Team in case of Out of Specification (OOS) findings and participate in OOS investigations as directed. Interpret USP and compendia procedures with direct supervision; participate in team discussions and contribute recommendations to improve procedures. Perform peer review of basic analytical testing; participate in all company training; perform other related duties as required. Communicate project status and issues with QC manager/supervisor; inform QC/manager supervisor of any quality-related issues in the laboratory. Qualifications
A minimum of an Associate Degree in Chemistry or related discipline, or 2+ years of related laboratory experience. Basic theoretical and practical knowledge of inorganic chemistry, organic chemistry, arithmetic, geometry, statistics, and algebra. Knowledge of English language structure, spelling, grammar; good interpersonal and communication skills (written and verbal). Ability to establish and maintain effective working relationships; attention to details; good adaptability and computer competency with Microsoft Office; legible handwriting. Ability to perform multiple tasks simultaneously and learn new analytical techniques. Comfortable in a fast-paced environment with the ability to adjust workload based on changing priorities; self-motivated. Work Conditions and Physical Requirements
This position requires a minimum of 40 hours per week over 5 days, with possible additional hours to meet project deadlines. Travel is not required. Wear proper protective equipment; exposure to loud sounds or distracting noise levels; exposure to contaminants or hazardous conditions while conducting analyses. Work within several feet of others in the laboratory; sit or stand for extended periods; be able to lift up to 25 pounds. May crawl or climb to perform maintenance on instruments; repetitive tasks with few breaks. Salary Range: $50,000-$60,000/year Note: The Company will explore and provide reasonable accommodations to assist any qualified individual with a disability in performing the essential functions of the job. Click Here to Apply Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
The Chemist Level 1 position must be able to understand, comply, and be familiarized with company policies. Chemist 1 must comply with CGMP, GLP, GDP and NJL safety policies. They must follow respective standard operation procedures and quality practices established by the Quality Assurance and Regulatory Affairs Departments. The position requires basic knowledge of chemistry and mathematics to solve problems and support analyses and techniques used in the laboratory. Responsibilities
Perform and document routine work assigned, including operating analytical instruments and performing wet chemistry analysis in compliance with standard operating procedures, compendial monographs, policies, and regulations. Abide by ALOCA principles (Attributable, legible, contemporaneous, original and accurate). Follow CGMP/GLP laboratory practices and documentation relevant to duties; comply with company requirements and regulations. Record and document observations and procedures in laboratory notebooks in accordance with GMP. Calibrate basic instruments as needed (e.g., analytical balances, pH meter). Operate trained and assigned common laboratory equipment and perform wet chemistry analyses. Prioritize tasks and manage workload to meet business needs and deadlines, including urgent, rush, and standard turnaround times. Maintain instruments and equipment as required/needed. Ensure testing and results are conducted and reported without compromising quality and released in a timely manner. Prepare test solutions and standardize volumetric solutions as needed. Ensure supplies and reagents are in stock; segregate expired chemicals; communicate with managers and QC Coordinator. Follow proper waste disposal and environmental regulations; maintain a safe, clean, and organized laboratory environment. Ensure fume hoods are maintained after use. Notify QC Manager, Technical Supervisor, or Quality Assurance Team in case of Out of Specification (OOS) findings and participate in OOS investigations as directed. Interpret USP and compendia procedures with direct supervision; participate in team discussions and contribute recommendations to improve procedures. Perform peer review of basic analytical testing; participate in all company training; perform other related duties as required. Communicate project status and issues with QC manager/supervisor; inform QC/manager supervisor of any quality-related issues in the laboratory. Qualifications
A minimum of an Associate Degree in Chemistry or related discipline, or 2+ years of related laboratory experience. Basic theoretical and practical knowledge of inorganic chemistry, organic chemistry, arithmetic, geometry, statistics, and algebra. Knowledge of English language structure, spelling, grammar; good interpersonal and communication skills (written and verbal). Ability to establish and maintain effective working relationships; attention to details; good adaptability and computer competency with Microsoft Office; legible handwriting. Ability to perform multiple tasks simultaneously and learn new analytical techniques. Comfortable in a fast-paced environment with the ability to adjust workload based on changing priorities; self-motivated. Work Conditions and Physical Requirements
This position requires a minimum of 40 hours per week over 5 days, with possible additional hours to meet project deadlines. Travel is not required. Wear proper protective equipment; exposure to loud sounds or distracting noise levels; exposure to contaminants or hazardous conditions while conducting analyses. Work within several feet of others in the laboratory; sit or stand for extended periods; be able to lift up to 25 pounds. May crawl or climb to perform maintenance on instruments; repetitive tasks with few breaks. Salary Range: $50,000-$60,000/year Note: The Company will explore and provide reasonable accommodations to assist any qualified individual with a disability in performing the essential functions of the job. Click Here to Apply Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr