QC Associate & Scientist Salary at Patheon By Thermo Fisher Scientific BETA

Job Description At EXP, we're driven to provide innovative solutions for the world's built and natural environments. As a team of engineers, architects, designers, scientists, creators and a community of professionals, we bring diverse and talented people together to solve the world's most complex challenges. Here, you join a team that leverages differences, harnesses their entrepreneurial spirit in an employee-owned company, that believes diversity is what gives us strength, seeks sustainable results and shares ambitions for each other, our clients and the communities we are part of and serve. To be a part of EXP means to have your own experience, while staying connected to a global network of professionals, who believe we are a part of something bigger. Together, we are EXP. Are you ready to design your future? Be our next Plumbing & Fire Protection Designer / Engineer! Your work environment at EXP In this role, you will be a part of the Plumbing and Fire Protection Design/Engineerin

We are seeking an Immunoassay Associate Scientist to join Q² Solutions, IQVIA's laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You'll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. What you'll be doing: Executing ELISAs, RIAs, and other immunoassay techniques in a BSL2 lab with precision and innovation. Learning required laboratory techniques under the guidance of the project leader. Perf

Pay to worker is BR. We are looking to markups of about 45%. There is some wiggle room built in. This is for a temp to perm position for around to 6 months. Conversion target amount is about 45K. In her/his function as QC Analytical Development Scientist, the person is responsible for the following: Execute GMP cleaning of critical spaces in accordance with Standard Operating Procedures on a daily basis. Execute emergency GMP cleaning of spaces that were identified to have had a contamination event or rooms that have gone out of temperature/ humidity specification. Ability to create and revise standard operating procedures. Coordinate with 3rd Party Cleaning vendor and ensures cleanings are completed as required. Inventory management - tracking PAR levels, ensuring materials are available, build manufacturing kits Receiving of material when needed. Participate in 10 hours of continuing education annually in cellular therapy or quality topics. Responsibilities may be modified or added a

Job Title: Associate ScientistJob Description A global CDMO in pharmaceutical manufacturing providing process characterization is seeking an Associate Scientist to support business influx leading to increased testing. Responsibilities + Perform HPLC, LC, and ELISA testing. + Handle liquid handling and robotics automation. + Utilize TECAN for liquid handling and automation tasks. + Ensure compliance with GMP/GLP standards. Essential Skills + 2-3 years of experience with HPLC, LC, and ELISA. + Experience with TECAN for liquid handling and automation. + 2-4 years of experience in a GMP/GLP laboratory. + BS/BA in science, preferably in chemistry, biochemistry, pharmaceutical sciences, or a related technical field. Additional Skills & Qualifications + Strong understanding of chemistry-based techniques. + Experience interacting with analytical development teams. Work Environment The site comprises three buildings supporting various parts of the global organization. The QC group, to which thi

Job Description Job Description Stability Research Scientist Clayton, NC M-F 8am-4:30pm ***Requires MS degree + 0-1 years, or BS degree + 1-2 years, or no degree + 5 years’ experience (degree in life sciences, work experience in clinical and/or pharma lab). Will be handling whole and/or partial blood products and other biological samples*** Description: The incumbent will work in a supporting function to provide scientific and technical assistance in the research and development of plasma derived or recombinant proteins. The position provides support to the Stability Group by overseeing all facets of the stability program that are related to oversight of the stability chamber areas, storage, delivery, and documentation of the sample inventory in order to maintain a compliant stability program for licensed products and developmental projects, ensuring on-going safety and quality of our products. Responsibilities of this position include but are not limited to: Daily, maintain product in

R&D Partners is seeking to hire an Associate Stability Research Scientist II in Clayton, NC. Your main responsibilities as a n Associate Stability Research Scientist II: · Daily, maintain product inventory for active stability studies in accordance with all compliance requirements by assuring the accountability and delivery of all stability samples and associated documentation as well as the issuance of required documentation for testing. · Coordinate with Packaging to acquire samples for batches to be placed into the stability program for evaluation. · Maintain label printers in good working order to ensure ability to fulfill printing of labels for stability requests. · Maintain and audit all sample labeling and documentation for accuracy and compliance with GMP. · Facilitate delivery of stability samples for laboratory testing and coordinate with QC Sample Specialists and stability supervisors to correct any discrepancies associated with stability samples for testing. What we are loo

Job Description Job Description Your main responsibilities as a Stability Research Scientist: · Daily, maintain product inventory for active stability studies in accordance with all compliance requirements by assuring the accountability and delivery of all stability samples and associated documentation as well as the issuance of required documentation for testing. · Coordinate with Packaging to acquire samples for batches to be placed into the stability program for evaluation. · Maintain label printers in good working order to ensure ability to fulfill printing of labels for stability requests. · Maintain and audit all sample labeling and documentation for accuracy and compliance with GMP. · Facilitate delivery of stability samples for laboratory testing and coordinate with QC Sample Specialists and stability supervisors to correct any discrepancies associated with stability samples for testing. What we are looking for: · This position requires MS Degree /BS + 1-2 years/No degree + 5

Our Client, a Pharmaceutical company, is looking for an Associate Stability Research Scientist II for their Clayton, NC location. Responsibilities: Daily, maintain product inventory for active stability studies in accordance with all compliance requirements by assuring the accountability and delivery of all stability samples and associated documentation as well as the issuance of required documentation for testing. Coordinate with Packaging to acquire samples for batches to be placed into the stability program for evaluation. Maintain label printers in good working order to ensure ability to fulfill printing of labels for stability requests. Maintain and audit all sample labeling and documentation for accuracy and compliance with GMP. Facilitate delivery of stability samples for laboratory testing and coordinate with QC Sample Specialists and stability supervisors to correct any discrepancies associated with stability samples for testing. Possess experience necessary to note any unchar