Chemical Engineer Salary at 3Chi BETA

Job Description: We are looking for a skilled Process Engineering Leader to join our client's team. The successful candidate will lead process improvement initiatives to enhance production efficiency and product quality. Key Responsibilities: Lead and manage the process engineering team. Develop and implement process improvements for manufacturing operations. Collaborate with R&D and production teams to optimize ingredient formulations. Ensure compliance with industry standards and safety regulations. Troubleshoot and resolve process-related issues. Qualifications: Bachelor's degree in Chemical Engineering, Process Engineering, or a related field. Proven experience in process engineering within the specialty ingredients or related industry. Strong leadership and project management skills. Excellent analytical and problem-solving abilities. Effective communication and teamwork skills.

About Curium Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name 'Curium' honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline 'Life Forward' represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.

Position Description: • Assist with HPLC analysis of materials (previous analytical experience desirable) • Support routine sample preparation and characterization • Compliance with laboratory safety procedures Other responsibilities include: • Be able to run and operate sample characterization instrumentation • Consistently applies sound scientific methods to solve technical problems. • Assist with qualifying new active ingredient and raw material sources and supports shelf life date extensions for existing products. Requirements: • Prior experience in research or manufacturing/engineering. • Strong interpersonal and collaboration skills. • Experience in a chemistry lab is desirable. • Excellent verbal and written communication skills. Ability to clearly articulate information and data sharing with stakeholders. Education • BS in Chemistry, Chemical Engineering, Analytical Chemistry or related fields • Experience with the design and development of formulations is desirable • This posi

Chemical Engineer – Design and Development D&M Continuous Solutions is seeking a talented and driven individual to join an industry leading firm in equipment design for pharmaceutical processes for research and manufacturing scale. We work with customers around the world to deliver equipment and innovative process designs to enable production of pharmaceutical products for traditional chemical engineering unit operations as well as specialized modalities such as peptides and oligonucleotides. Key responsibilities: The engineer has a diverse set of responsibilities, some examples include: · Create engineering drawings and perform calculations around equipment sizing and design. · Provides engineering support for equipment platforms through application of chemical engineering fundamentals. · Perform lab experiments in parallel with equipment development to support customer projects for small molecule, peptides, or oligonucleotides at a variety of scales. · Perform minor coding updates or

BCforward is seeking a highly motivated Document Controller to support their pharmaceutical client’s new site build in Lebanon, IN. Expected Duration: Long Term Location: Lebanon, IN/onsite Overview: In support of our Client's newest Plant site, we are seeking to hire a highly skilled professional with exceptional expertise in Microsoft Word formatting and a comprehensive understanding of supporting site start-up projects. Demonstrated mastery in Microsoft Word, able to support operational readiness and facilitate effective communication and coordination will be important. This Plant Facility will represent the “facility of the future” and as such be lean, environmentally conscious, efficient in the design and operation, and enabling quality excellence. The Document Controller will be expected to work onsite at both Lebanon, IN, and Indianapolis, IN locations and support multiple departments. This position will report to site operation or quality lead. Focus All related activities will

Overview: We have a career opportunity for a Manager Process Control and Compliance to join our team! Incumbent reports to the Director of Wastewater Plant Operations and collaborates with the Manager Wastewater Operations, Manager Wastewater Maintenance, Wastewater Collections department, and Environmental Stewardship department. Responsible for management of the Solids Handling Facility, Septage Receiving Station, Lift Station 507, and Eagle Creek Dam. Manages a staff of approximately 11 non-bargaining employees and 22 bargaining employees. Ensures all wastewater treatment processes comply with local, state, and federal regulations. Implements and monitors process control systems needed to achieve consistent and efficient wastewater treatment. Manages the generation, review, and timely submittal of compliance reporting for the NPDES and Title V permits. Identifies and implements continuous improvement activities to enhance efficiency, reduce costs, and improve treatment outcomes. Mus

Job Title: Pharmaceutical Process Engineer Location: Indianapolis, IN Hire Type: Onsite, Long-Term Contract Target Pay Range: $60.00 - $80.00/hour (W2 with full employee benefits) Overview: Sterling has helped build careers for thousands of professionals like yourself. Our expert recruiters support you at every step in the process and as a Best of Staffing company, Sterling provides exciting work with exceptional employers across the U.S. As a contract employee of Sterling, you are eligible to receive a Full Employee Benefits Package that includes paid time off, paid holidays, 3 medical plans to choose from, dental & vision plans, 401(k), and an Employee Stock Ownership (ESOP) plan. Job Summary: This long-term contract position will play a vital role in supporting manufacturing operations within a pharmaceutical production setting by implementing strong technical solutions and driving process enhancements. The ideal candidate will bring extensive expertise in pharmaceutical manufacturi

Document Control Supervisor INCOG Biopharma Services in Indianapolis, IN is hiring a Document Control Supervisor. INCOG is seeking a Supervisor that will be instrumental in developing and championing INCOG’s approach to the design, approachability, control, and training of content; ultimately being a major contributor for the Integrity of the management of data/information at the site. The Supervisor will manage the team responsible for the flow of documents, records, and subject matter experts, and own the logistical operations for all site inspections. The primary function of this role will be to manage the Document Control team, and be responsible for the flow of documents, records, and subject matter experts, and own the logistical operations for all site inspections. There is a growing need globally for more CDMOs (contract development and manufacturing organization) in the pharmaceutical industry to provide comprehensive services from drug development through drug manufacturing.