Controller Salary at Inspire Environmental BETA

Quality Control Chemist Company Information: Tedor is a privately held pharmaceutical company a CDMO that develops drug product for both innovator and established companies. We are customer-focused oral solid dose CDMO with a strong track record of meeting aggressive development and commercialization timelines Over the past 20 years we have helped customers received many product approvals.We attribute this success to our company-wide focus on quality, customer service, and meeting timelines. Everything we do, and how we do it, is focused on helping our clients to achieve their product objectives. Position Summary: The role of the Quality Control Chemist is a vital role that is essential to manage and execute the quality testing that is required for drug substance on the commercial market. Quality Control Chemist will also be responsible for method validation and release & stability testing for clinical trial and commercial drug products; therefore, verifying all products and/or substan

About the Role: We are seeking an experienced QC Chemist II to join a dynamic pharmaceutical quality control team. This role is ideal for professionals with 3-5 years of hands-on laboratory experience in a GMP-regulated environment. If you’re looking to expand your expertise in analytical testing and contribute to high-quality pharmaceutical manufacturing, this opportunity is for you! Key Responsibilities: Perform routine and advanced analytical testing on raw materials, in-process samples, and finished pharmaceutical products. Operate and maintain laboratory instruments, including HPLC, GC, KF, Dissolution, Particle Size Analysis, and ICP. Support laboratory investigations, method development, and troubleshooting activities. Ensure compliance with cGMP, GLP, data integrity standards, and good documentation practices. Assist in training and mentoring junior chemists as needed. Collaborate with cross-functional teams to ensure testing timelines are met. What You Need to Succeed: Educati

-Pay: 41hr -10 month contract The role requires flexibility for weekend coverage to support a continuous operational schedule. This is a first shift position Friday-Monday (4 x 10 hours), but will require an initial period of Monday-Friday work to accommodate training. The Quality Control Operations (QCO) Analyst III Contractor plays a crucial role in supporting the department's efforts to maintain the highest standards of quality and compliance from development through to commercialization. In addition to executing routine and non-routine testing in support of development through commercial programs, the Analyst III will also participate in data trending, investigations, and laboratory operations. This position will also play a role in method transfers, method qualification/validation, verification, and implementation. By ensuring these critical activities are executed with precision, the Analyst III significantly contributes to routine laboratory operations, thereby enhancing the ove

About the Role: Are you a recent graduate or early-career professional looking to launch your career in pharmaceutical quality control? We are hiring QC Chemist I candidates for a fast-growing pharmaceutical company. This is a fantastic opportunity to gain hands-on experience in a regulated laboratory environment, working with cutting-edge equipment and a team of industry professionals. Key Responsibilities: Conduct routine quality control testing on raw materials, in-process samples, and finished pharmaceutical products. Utilize laboratory instruments such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Karl Fischer (KF), and Dissolution testing. Follow standard operating procedures (SOPs) while ensuring compliance with cGMP, GLP, and data integrity regulations. Document test results accurately and maintain detailed laboratory records. Work collaboratively within the team to meet testing deadlines and support investigations when needed. Maintain laboratory e

Job Description Be part of the future! Let's Build a better Tomorrow Together! We are one team, dedicated to working together to create the purposeful solutions that propel the world forward. We hope you will join our diverse team of top people – you bring your talent, and we’ll give you the space and opportunities to grow and succeed. We are passionate about making a difference! What we offer Competitive salary Paid vacation/holidays/sick time Comprehensive benefits package including 401K, medical, dental, and vision care Extensive product and on the job/cross training opportunities with outstanding resources Encouraging and collaborative team environment Dedication to safety through our Zero Harm policy Company vehicle, Tools and Equipment to complete all jobs Providing Scheduling and management support What you will do Perform HVAC Control systems programming, troubleshooting, installation, commissioning and preventative maintenance as it is related to mechanical, electrical, and lo

Job Description Job Description Duties: Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations Qualifications: B.S. in chemistry, biology, or biochemistry, or related scientific field Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent, relevant industry experience Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirabl Proficiency in LabWare LIMS, Excel, Word, and PowerPoint pr

Controls Engineer Location: Taunton, Massachusetts This position offers an opportunity to make an immediate impact by driving projects to successful completion. It is ideal for a motivated professional looking to help manufacturing industries enhance their competitive advantage and achieve energy efficiency goals. The role is within an organization of engineers, owned and managed by fellow engineers, that provides automation solutions across various industries, including chemicals, pharmaceuticals, industrial gases, and discrete manufacturing. Job Overview The Controls Engineer will be responsible for delivering projects to customers, with key responsibilities including: Designing, developing, and documenting systems that meet customer requirements. Identifying gaps in existing OT networks and computing systems, providing risk-based recommendations for improvement. Communicating with customers both on-site and remotely to present work and develop tailored solutions. Designing and imple

Job Description Job Description Open to a recent graduate or someone with 0-2 years of related experience. Must Have: Baseline industry knowledge in Pharma. Possibly a candidate who took relevant coursework in college. Nice to have: Testing or lab experience around analytical instruments in quality control testing. Experience: • Bachelor’s degree and 2 years of Quality/ Operations Experience OR • Associate's degree and 3+ years of Quality/ Operations Experience o OR • High school diploma/GED and 4+ years of Quality/ Operations Experience Preferred Qualifications • GMP and GDP experience in a laboratory setting. • Proficient in Trackwise, Maximo, CDOCS • Experienced in Quality systems, including Change Control, Deviations, CAPA • Experienced in Quality processes, including validation and data integrity • Proficient in problem solving and LEAN principles Company Description Collabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-