Direct message the job poster from Piramal Pharma Solutions
UK and USA Senior Talent Acquisition Partner l Headhunter l Global l Pharma.
Analytical Development Scientist responsible for analytical method development, validation, technical transfer and routine Quality Control support. Role Departmental Operations: Perform assigned work as agreed with the project lead and/or Analytical Development Manager. Ensure efficient use of time to complete the assigned objectives. Maintain laboratory areas, ensuring procedures are complied with to meet client, regulatory GMP and safety requirements. Provide training and troubleshooting support to production and stability Quality Control groups. Provide QC support (if required). Engage in specified compliance and improvement projects. Provide cover for other Analytical Development Scientists as required. Ensure economic use of labour, materials, energy and services, proposing and implementing measures for cost reduction and waste minimisation to meet the department and site targets. Identify opportunities for improved methods of working to enhance efficiency, cost control and safety/GMP performance. Support training of new members of staff to the company / department. Project Delivery: Responsible for ensuring that assigned project deliverables are fully completed on time. Lead aspects of projects as appropriate and in agreement with the Analytical Development Manager. Plan and carry out work, as agreed with the project lead, to ensure effective project progression in line with customer requirements. Support method development, technical transfer, qualification and validation activities. Provide analytical development project support, ensuring compliant introduction into QC, production and stability groups – have involvement in decisions on scheduling of development, technical transfer and validation in conjunction with other technical staff. Workload planning with other staff to ensure required timelines are met. Provide QC support if required. Client communication as required, in a professional manner. Quality: Ensure timely close out of deviations, change controls and commitment tracking. Uphold cGMP principles and ESH standards, continually seek opportunities to improve and enhance standards, and encourage other staff to do likewise. Record all laboratory work in standard official notebooks and compile results and observations for incorporation into technical reports. Adhere to the relevant procedures. Follow all appropriate protocols and procedures as required for the work undertaken. Ensure accuracy of raw data and analytical interpretations. Seniority level
Associate Employment type
Full-time Job function
Science and Other Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
Analytical Development Scientist responsible for analytical method development, validation, technical transfer and routine Quality Control support. Role Departmental Operations: Perform assigned work as agreed with the project lead and/or Analytical Development Manager. Ensure efficient use of time to complete the assigned objectives. Maintain laboratory areas, ensuring procedures are complied with to meet client, regulatory GMP and safety requirements. Provide training and troubleshooting support to production and stability Quality Control groups. Provide QC support (if required). Engage in specified compliance and improvement projects. Provide cover for other Analytical Development Scientists as required. Ensure economic use of labour, materials, energy and services, proposing and implementing measures for cost reduction and waste minimisation to meet the department and site targets. Identify opportunities for improved methods of working to enhance efficiency, cost control and safety/GMP performance. Support training of new members of staff to the company / department. Project Delivery: Responsible for ensuring that assigned project deliverables are fully completed on time. Lead aspects of projects as appropriate and in agreement with the Analytical Development Manager. Plan and carry out work, as agreed with the project lead, to ensure effective project progression in line with customer requirements. Support method development, technical transfer, qualification and validation activities. Provide analytical development project support, ensuring compliant introduction into QC, production and stability groups – have involvement in decisions on scheduling of development, technical transfer and validation in conjunction with other technical staff. Workload planning with other staff to ensure required timelines are met. Provide QC support if required. Client communication as required, in a professional manner. Quality: Ensure timely close out of deviations, change controls and commitment tracking. Uphold cGMP principles and ESH standards, continually seek opportunities to improve and enhance standards, and encourage other staff to do likewise. Record all laboratory work in standard official notebooks and compile results and observations for incorporation into technical reports. Adhere to the relevant procedures. Follow all appropriate protocols and procedures as required for the work undertaken. Ensure accuracy of raw data and analytical interpretations. Seniority level
Associate Employment type
Full-time Job function
Science and Other Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
