Workforce Signals

Normalized fields

open

Function: digital_it
Business unit: Not classified
Location: Not provided
Work model: Not classified
Seniority: Not classified
Clearance: Not provided
Employment type: Not provided
Compensation: Not provided
First seen: 2026-09-25T06:00:48.552Z
Last seen: 2026-10-12T06:00:33.956Z
Requisition: JB-242

Latest version

MediWound is seeking a motivated and scientifically driven Pharmaceutical and nonclinical development project manager to join our Pharmaceutical and nonclinical R&D team and contribute to multidisciplinary pharmaceutical development activities. The role spans multiple areas, including scientific studies, development of new drug product formulations and manufacturing processes, sterilization-related activities, and development and validation of new methods. The position combines hands-on scientific work with study planning, data analysis, scientific documentation, collaboration with external CROs, and coordination with internal functions. The development activities span from early concept and formulation through CMC development for clinical trials, continued support throughout clinical development, and preparation for product approval. The successful candidate will contribute to moving development projects from scientific questions through execution, interpretation, and reporting, in accordance with project timelines and relevant regulatory requirements. The role includes project management responsibilities and does not involve direct management of a team. Responsibilities: Design and execute experiments related to formulation and process development, scientific and biochemical studies, method development, and GMP validation activities. Prepare study plans and protocols based on regulatory guidelines, scientific knowledge, literature review, project objectives, timelines, and budget. Perform hands-on laboratory work, including formulation preparations and aseptic work. Develop, qualify, and validate new methods and processes in accordance with relevant regulatory guidelines and project needs. Process, analyze, interpret, and present scientific data; maintain complete raw-data records and write clear protocols, reports, and development documentation. Identify scientific and operational challenges, troubleshoot issues, and support the improvement of processes and methods. Coordinate activities with external CROs and service providers, including scope definition, progress follow-up, performance monitoring, and review of results, as applicable. Collaborate with internal interfaces, including Analytical R&D, Operations, QA, and Regulatory Affairs, to advance project activities and deliverables. Support regulatory activities and submissions related to pharmaceutical and nonclinical development projects. Manage priorities and multiple scientific activities in parallel while meeting agreed timelines. Requirements: Ph.D. in Chemistry, Biochemistry, Pharmacology, Biotechnology, Biotechnology Engineering, or a related scientific field with at least 3 years R&D experience in the pharmaceutical or biotechnology industry, or M.Sc with at least 6 years R&D experience in the pharmaceutical or biotechnology industry Experience leading scientific and pharmaceutical development projects, formulation development or manufacturing-process development, preferably at clinical or commercial stages. Knowledge of pharmaceutical development guidelines, including GMP, GLP, and ICH, and familiarity with process and method validation principles. Experience working with and managing CROs or other external service providers. Strong scientific orientation and problem-solving ability, with the capacity to learn and work across different scientific disciplines. Strong organizational skills, attention to detail, and the ability to manage several activities in parallel. Excellent scientific writing, communication, and interpersonal skills. Self-motivated, collaborative, and able to work independently in a dynamic environment. Fluent English, spoken and written. Advantages Experience with aseptic techniques and biochemical or enzymatic assays. Experience with biologically derived or enzyme-based products. Experience with sterile drug products, sterilization of excipients or raw materials, packaging development, or Container Closure Integrity Testing. Experience with Design of Experiments and statistical data analysis.

Content hash: d103042550a935c6de261a633fe9bd5b3c2dad4f231d70b68af19d86cf7417ba

Derived classifications

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  "entities_programs": [],
  "business_categories": [
    {
      "value": "engineering",
      "evidence": [
        "equirements: Ph.D. in Chemistry, Biochemistry, Pharmacology, Biotechnology, Biotechnology Engineering, or a related scientific field with at least 3 years R&D experience in the pharmaceutical"
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      "confidence": "high"
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    {
      "value": "digital_it",
      "evidence": [
        "ation of new methods. The position combines hands-on scientific work with study planning, data analysis, scientific documentation, collaboration with external CROs, and coordination wi"
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      "confidence": "high"
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    {
      "value": "program_management",
      "evidence": [
        "seeking a motivated and scientifically driven Pharmaceutical and nonclinical development project manager to join our Pharmaceutical and nonclinical R&D team and contribute to multidisciplinary p"
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      "confidence": "high"
    }
  ]
}

Version history

2 retained

Version 22026-09-29T06:00:32.006Z{"description":{"after":{"description_text":"MediWound is seeking a motivated and scientifically driven Pharmaceutical and nonclinical development project manager to join our Pharmaceutical and nonclinical R&D team and contribute to multidisciplinary pharmaceutical development activities. The role spans multiple areas, including scientific studies, development of new drug product formulations and manufacturing processes, sterilization-related activities, and development and validation of new methods.\nThe position combines hands-on scientific work with study planning, data analysis, scientific documentation, collaboration with external CROs, and coordination with internal functions. The development activities span from early concept and formulation through CMC development for clinical trials, continued support throughout clinical development, and preparation for product approval. The successful candidate will contribute to moving development projects from scientific questions through execution, interpretation, and reporting, in accordance with project timelines and relevant regulatory requirements. The role includes project management responsibilities and does not involve direct management of a team.\nResponsibilities:\nDesign and execute experiments related to formulation and process development, scientific and biochemical studies, method development, and GMP validation activities.\nPrepare study plans and protocols based on regulatory guidelines, scientific knowledge, literature review, project objectives, timelines, and budget.\nPerform hands-on laboratory work, including formulation preparations and aseptic work.\nDevelop, qualify, and validate new methods and processes in accordance with relevant regulatory guidelines and project needs.\nProcess, analyze, interpret, and present scientific data; maintain complete raw-data records and write clear protocols, reports, and development documentation.\nIdentify scientific and operational challenges, troubleshoot issues, and support the improvement of processes and methods.\nCoordinate activities with external CROs and service providers, including scope definition, progress follow-up, performance monitoring, and review of results, as applicable.\nCollaborate with internal interfaces, including Analytical R&D, Operations, QA, and Regulatory Affairs, to advance project activities and deliverables.\nSupport regulatory activities and submissions related to pharmaceutical and nonclinical development projects.\nManage priorities and multiple scientific activities in parallel while meeting agreed timelines.\nRequirements:\nPh.D. in Chemistry, Biochemistry, Pharmacology, Biotechnology, Biotechnology Engineering, or a related scientific field with at least 3 years R&D experience in the pharmaceutical or biotechnology industry, or M.Sc with at least 6 years R&D experience in the pharmaceutical or biotechnology industry\nExperience leading scientific and pharmaceutical development projects, formulation development or manufacturing-process development, preferably at clinical or commercial stages.\nKnowledge of pharmaceutical development guidelines, including GMP, GLP, and ICH, and familiarity with process and method validation principles.\nExperience working with and managing CROs or other external service providers.\nStrong scientific orientation and problem-solving ability, with the capacity to learn and work across different scientific disciplines.\nStrong organizational skills, attention to detail, and the ability to manage several activities in parallel.\nExcellent scientific writing, communication, and interpersonal skills.\nSelf-motivated, collaborative, and able to work independently in a dynamic environment.\nFluent English, spoken and written.\nAdvantages\nExperience with aseptic techniques and biochemical or enzymatic assays.\nExperience with biologically derived or enzyme-based products.\nExperience with sterile drug products, sterilization of excipients or raw materials, packaging development, or Container Closure Integrity Testing.\nExperience with Design of Experiments and statistical data analysis."},"before":{"description_text":"MediWound is seeking a motivated and scientifically driven Pharmaceutical R&D Scientist to join our Pharmaceutical and nonclinical R&D team and contribute to multidisciplinary pharmaceutical development activities. The position is open to candidates at different career stages, and its scope, level of independence, and project leadership responsibilities will be determined according to the selected candidate’s experience.\nThe role spans multiple areas, including scientific studies, development of new drug product formulations and manufacturing processes, sterilization-related activities, and development and validation of new methods.\nThe position combines hands-on scientific work with study planning, data analysis, scientific documentation, collaboration with external CROs, and coordination with internal functions. The development activities span from early concept and formulation through CMC development for clinical trials, continued support throughout clinical development, and preparation for product approval. The successful candidate will contribute to moving development projects from scientific questions through execution, interpretation, and reporting, in accordance with project timelines and relevant regulatory requirements.\nResponsibilities:\nDepending on experience, take scientific ownership of assigned projects and lead their planning, execution, timelines, external collaborations, and documentation.\nDesign and execute experiments related to formulation and process development, scientific and biochemical studies, method development, and GMP validation activities.\nPrepare study plans and protocols based on regulatory guidelines, scientific knowledge, literature review, project objectives, timelines, and budget.\nPerform hands-on laboratory work as required, including formulation preparations and aseptic work.\nDevelop, qualify, and validate new methods and processes in accordance with relevant regulatory guidelines and project needs.\nProcess, analyze, interpret, and present scientific data; maintain complete raw-data records and write clear protocols, reports, and development documentation.\nIdentify scientific and operational challenges, troubleshoot issues, and support the improvement of processes and methods.\nCoordinate activities with external CROs and service providers, including scope definition, sample preparation and shipment, progress follow-up, performance monitoring, and review of results, as applicable.\nCollaborate with internal interfaces, including Analytical R&D, Operations, QA, and Regulatory Affairs, to advance project activities and deliverables.\nSupport regulatory activities and submissions related to pharmaceutical and nonclinical development projects.\nContribute to the operational management of the laboratory, including inventory, sourcing and ordering materials, budget follow-up, and equipment maintenance, calibration, and service scheduling.\nManage priorities and multiple scientific activities in parallel while meeting agreed timelines.\nRequirements:\nM.Sc. in Chemistry, Biology, Biochemistry, Pharmacology, Biotechnology, Biotechnology Engineering, or a related scientific field.\nHands-on laboratory experience gained in an academic, biotechnology, or pharmaceutical setting.\nStrong scientific orientation and problem-solving ability, with the capacity to learn and work across different scientific disciplines.\nAbility to work accurately according to written protocols and to document experimental work and results clearly.\nStrong organizational skills, attention to detail, and the ability to manage several activities in parallel.\nExcellent scientific writing, communication, and interpersonal skills.\nSelf-motivated, collaborative, and able to work independently in a dynamic environment.\nFluent English, spoken and written.\nAdvantages\nPh.D. in a relevant scientific field.\nR&D experience in the pharmaceutical industry, including experience leading scientific and pharmaceutical development projects.\nExperience in formulation development, manufacturing-process development, or method validation.\nExperience with aseptic techniques and biochemical or enzymatic assays.\nExperience with biologically derived or enzyme-based products.\nKnowledge of pharmaceutical development guidelines, including GMP, GLP, and ICH, and familiarity with process and method validation principles.\nExperience with sterile drug products, sterilization of excipients or raw materials, packaging development, or Container Closure Integrity Testing.\nExperience working with and managing CROs or other external service providers.\nExperience with Design of Experiments and statistical data analysis."}}}

{
  "added": [
    "MediWound is seeking a motivated and scientifically driven Pharmaceutical and nonclinical development project manager to join our Pharmaceutical and nonclinical R&D team and contribute to multidisciplinary pharmaceutical development activities.",
    "The role includes project management responsibilities and does not involve direct management of a team.",
    "Responsibilities: Design and execute experiments related to formulation and process development, scientific and biochemical studies, method development, and GMP validation activities.",
    "Perform hands-on laboratory work, including formulation preparations and aseptic work.",
    "Coordinate activities with external CROs and service providers, including scope definition, progress follow-up, performance monitoring, and review of results, as applicable.",
    "Requirements: Ph.D.",
    "in Chemistry, Biochemistry, Pharmacology, Biotechnology, Biotechnology Engineering, or a related scientific field with at least 3 years R&D experience in the pharmaceutical or biotechnology industry, or M.Sc with at least 6 years R&D experience in the pharmaceutical or biotechnology industry Experience leading scientific and pharmaceutical development projects, formulation development or manufacturing-process development, preferably at clinical or commercial stages.",
    "Knowledge of pharmaceutical development guidelines, including GMP, GLP, and ICH, and familiarity with process and method validation principles.",
    "Experience working with and managing CROs or other external service providers.",
    "Advantages Experience with aseptic techniques and biochemical or enzymatic assays."
  ],
  "removed": [
    "MediWound is seeking a motivated and scientifically driven Pharmaceutical R&D Scientist to join our Pharmaceutical and nonclinical R&D team and contribute to multidisciplinary pharmaceutical development activities.",
    "The position is open to candidates at different career stages, and its scope, level of independence, and project leadership responsibilities will be determined according to the selected candidate’s experience.",
    "Responsibilities: Depending on experience, take scientific ownership of assigned projects and lead their planning, execution, timelines, external collaborations, and documentation.",
    "Design and execute experiments related to formulation and process development, scientific and biochemical studies, method development, and GMP validation activities.",
    "Perform hands-on laboratory work as required, including formulation preparations and aseptic work.",
    "Coordinate activities with external CROs and service providers, including scope definition, sample preparation and shipment, progress follow-up, performance monitoring, and review of results, as applicable.",
    "Contribute to the operational management of the laboratory, including inventory, sourcing and ordering materials, budget follow-up, and equipment maintenance, calibration, and service scheduling.",
    "Requirements: M.Sc.",
    "in Chemistry, Biology, Biochemistry, Pharmacology, Biotechnology, Biotechnology Engineering, or a related scientific field.",
    "Hands-on laboratory experience gained in an academic, biotechnology, or pharmaceutical setting.",
    "Ability to work accurately according to written protocols and to document experimental work and results clearly.",
    "Advantages Ph.D.",
    "in a relevant scientific field.",
    "R&D experience in the pharmaceutical industry, including experience leading scientific and pharmaceutical development projects.",
    "Experience in formulation development, manufacturing-process development, or method validation.",
    "Experience with aseptic techniques and biochemical or enzymatic assays.",
    "Knowledge of pharmaceutical development guidelines, including GMP, GLP, and ICH, and familiarity with process and method validation principles.",
    "Experience working with and managing CROs or other external service providers."
  ]
}

Version 12026-09-25T06:00:48.552ZInitial version