Analytical/organic Chemistry
I am looking for phd level who knows hplc , analytical chemistry statistics , adsorption mechanisms etc .
+33 Other ResponsesQuality Control Director
Oversee day to day operations of the quality control, document management, raw materials and stability groups. Works closely with managers to ensure testing operations are performed, including capacity management, metrics and execution of testing. Maintains rigorous quality mindset and advocates strict adherence to compliance practices within the testing labs and facility. Possess scientific skills in the specific science area and a strong working knowledge of the technical, usp compendial testing, and current good manufacturing practice (cgmp) compliance requirements for in-process, raw materials and product quality testing. Remains current regarding product quality testing needs for biosimilars and works with the technical teams to develop / modify assays to meet requirements. Ensures that appropriate records are maintained according to and in compliance with fda guidelines for biosimilars, usp, glp, cgmp, code of federal regulations (cfr) and/or points to consider (ptc) guidelines, ich guidelines, and sops. Works closely with the analytical research and development team to receive and validation of new assays and technologies, as well as existing assays. responsibilities:
ensures quality control testing is scheduled and performed develops and manages to operational and performance metrics supervises, plans and reviews operations for assigned staff, including responsibility for training, managing and evaluating as well as coordinating, scheduling and assigning work and maintaining standards recommends hire / transfer / promotion / discharge and salary changes and acts on employee problems conducts employee performance appraisals in a timely and objective manner may act as study director for assigned assays and assumes all associated responsibilities interacts with other functional groups to discuss project planning and testing issues works with the analytical research and development team to provide strong in-house guidance on science and technology interacts with internal staff to identify assays requiring further improvement or development responsible for appropriately conducting assays in accordance with cgmps assures that laboratory personnel are following all company sops and safety rules prepares and revises technical documents (laboratory protocols, change controls, oos investigations, capas, sops, etc.) assures that test batch records and deviations, oos results, qa audits and other paperwork are completed according to cgmps and company sops
qualifications:
ph.D. In biochemistry/analytical chemistry with 10 years or bs or ms with 15 years quality control industry experience must have 8 or more years of experience with proteins and antibodies knowledge of cgmp and biosimilars guidelines is desirable ability to make decisions based on a wide knowledge of factors where application of advanced or technical concepts is predominantly required ability to evaluate technical data and write technical documents ability to use judgment as dictated by complexity of situation ability to work under limited supervision and to handle problems of a difficult nature ability to accomplish the described duties through the use of appropriate laboratory equipment (i.E. Biohazard hood, centrifuge, incubator, and autoclave) and computer equipment and software. (i.E. Microsoft word, outlook)
+40 Other ResponsesLarge Molecule Bioanalysis Cro Pricing
1. Can you provide the min – max (or) average pricing (in usd) for established/large cros (covance/labcorp, eurofins, wuxi) versus emerging/mid-size players (ait biosciences/nexelis, bioagilytix, frontage labs) for molecular bioanalysis services in the usa and western europe ?
2. What are the strategies cros have in place in an attempt to differentiate their large molecule bioanalysis services from each other to remain competitive?
3. Why is there a difference in pricing among cros (if applicable)? What is the delta between the low-cost services vs those pricing at the high-end range? Which cost component makes the service cost high or low?
4. What is the delta between the low-cost services vs those pricing at the high-end range by services of large molecule bioanalysis? Which cost component within each of the below service makes the cost high or low?
Kindly let me know your effort estimate and timeline for providing the above information. I will send an expert questionaire post this. Also, the deadline for receiving the info is 25th september 2021.
Awaiting your kind reply.
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kind regards
+5 Other Responses