Chemist Salary at Lawter Inc BETA

Job Summary Performs chemical analysis/laboratory testing of active pharmaceutical ingredients, in-process materials, finished products and stability materials per established methods. Responsible for Laboratory instrumentation set-up, troubleshooting, and routine maintenance. Supports work related to production, R&D, and NDA/ANDA filings. Job Description Responsibilities: Interpret USP or other compendia methods. Analyze raw materials, pharmaceutical ingredients, and finished products, including stability testing. Conduct laboratory activities with limited supervision. Maintain accurate record of all analyses performed, documenting test results in laboratory notebooks as required by GLP/cGMP. Write, review, and/or update Standard Operating Procedures as assigned. Evaluate new technologies, products, and materials as assigned by the Laboratory Manager, as well as other projects. Conduct notebook review and ensure CofA’s are submitted to the customer in a timely manner. Assist in the tr

job summary: A research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: $30 - 35 per hour work hours: 9 to 5 education: Bachelors responsibilities: Develop, analyze, and troubleshoot HPLC methods. Understand and apply different chromatographic modes (RPLC, NPLC, Polar organic, etc.) to optimize chromatographic separations Apply chromatographic software such as ChromSword, Drylab, and/or Fusion to optimize HPLC separations for deeper analysis Ensure GxP compliant delivery of high-quality data in a regulated environment Effectively communicate conclusions/findings to larger groups Develop protocols for more complex test

Work schedule: • Shift- 2pm-10pm Description: Independently performs and verifies a multitude of laboratory techniques for which they are trained on while adjusting to unforeseen technical or logistical obstacles to accomplish assignments. Understands multiple laboratory techniques and principles and can independently trouble-shoot and resolve analytical techniques and instrument issues. Takes initiative to be a key player in team activities and decision making including proactive identification, development, and implementation of improvement plans. Budgets their time independently and effectively to carry out assigned tasks and makes recommendations for improvement. Recognizes obstacles to completion of assigned testing and can independently resolve them. Consistently achieves commitments despite obstacles. Takes ownership of special projects as needed to support overall laboratory needs and requirements. Communicates proactively with supervisor and team members on frequent basis to e

Job Summary Performs chemical analysis/laboratory testing of active pharmaceutical ingredients, in-process materials, finished products and stability materials per established methods. Responsible for Laboratory instrumentation set-up, troubleshooting, and routine maintenance. Supports work related to production, R&D, and NDA/ANDA filings. Job Description Responsibilities: Interpret USP or other compendia methods. Analyze raw materials, pharmaceutical ingredients, and finished products, including stability testing. Conduct laboratory activities with limited supervision. Maintain accurate record of all analyses performed, documenting test results in laboratory notebooks as required by GLP/cGMP. Write, review, and/or update Standard Operating Procedures as assigned. Evaluate new technologies, products, and materials as assigned by the Laboratory Manager, as well as other projects. Conduct notebook review and ensure CofA's are submitted to the customer in a timely manner. Assist in the tr

Product Development Science and Technology (PDS&T), Analytical Development - Lake County (AD-LC) is a global analytical sciences organization responsible for all CMC analytical activities related to the development of therapeutic biologic products. Our scope includes diverse pipeline of innovative therapeutic biologics medicines, including monoclonal antibodies, antibody drug conjugates (Client), and other modalities, and spans support from clinical proof of concept through the transition of analytical methods and testing to commercial labs to support product launch. The Analytical Development - Lake County group within PDS&T is responsible for support of programs that are preparing for commercial development. The team leads commercial method development, optimization, robustness, and validation. In collaboration with cross-functional partners, the team supports commercial formulation and process development studies. The team also leads tech transfer of final methods to commercial test

Excellent Pay and Benefits! Opportunity for Growth! About Our Client A Chemical Manufacturer Job Description Conducts independent application testing of various products using standard testing methods or through coating experiments designed by others. Ensures timely completion of product development projects, adhering to departmental guidelines and priorities established by the supervisor. Operates laboratory equipment and apparatus efficiently, maintaining a clean and safe environment. Accurately documents, organizes, and communicates experimental results and testing data. Analyzes data, interprets test outcomes, and provides product recommendations to customers. Actively participates in troubleshooting and provides technical support to the sales team and customers. Maintains laboratory and storage areas, ensuring equipment is properly cared for. Complies with all applicable waste management procedures. May offer technical training to colleagues. Suggests and performs both short-term

Job Description: The Analytical Development-Early-Stage group within Biologics ARD is responsible for support of programs that are preparing for FIH clinical studies. The team leads Stage 1 method development, optimization, and validation. In collaboration with cross-functional partners, the team supports early phase formulation and process development studies. Key deliverables include product control strategies informed by analytical data and method understanding; robust analytical methods suitable for commercial QC labs; comprehensive data packages that drive product and process understanding; clinical supplies release testing and stability studies to establish clinical product dating; substantial clinical trial application submission content. Responsibilities: Laboratory operational support for the group's experimental development and testing activities. Complex solution preparation in a GxP environment. Laboratory balance checks and pH meter standardizations. Inventory/resource man

Application Chemist Every day, Kelly Science & Clinical connects professionals with opportunities to advance their careers. We currently have exciting temporary opportunity as an Application Chemist with a global leader in the production of high-performance coatings in Itasca, IL. Location: Itasca IL, relo support provided Duration: Direct Hire Schedule: M-F, 1st shift Compensation: $85,000-$95,000, candidates with more experience/higher compensation requests encouraged to apply as range is flexible based on experience! Summary: This job will focus on developing and testing water-based barrier coatings for paper and film (Oil and grease resistance/ Moisture vapor resistance / Oxygen transmission rate) As an Application Chemist you'll conduct on-time application testing, performance evaluation, data analysis and prepare technical reports of various products. Provides technical support including product recommendation, formulation support or troubleshooting for sales teams and customers.