8 Jobs für Drug Formulation Specialist
Stellenangebote Drug Formulation Specialist Jobs
Job gestern bei Jooble gefunden
mbiomics GmbH
• München
POSITION SUMMARY The Senior Scientist, Biological Process Development is a highly skilled and collaborative team member responsible for designing, executing, and interpreting experiments that advance
drug substance process development for [...]
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[...] the companys live biotherapeutic product (LBP) pipeline. This role spans both upstream and downstream processing activities for drug substance-from fermentation optimization and scale-up through harvest, concentration, lyophilization, and preparation for drug product manufacturing. In addition to strong bench science capabilities, the Senior Scientist will play an active role in coordinating technical activities with external contract development and manufacturing organizations (CDMOs) and specialist vendors, serving as an informed day-to-day liaison between internal development programs and the external partner network. KEY RESPONSIBILITIES Process Development Design and execute fermentation development experiments using bench-top and pilot-scale bioreactors, including operation of anaerobic culture systems appropriate for LBP organisms. Optimize culture media, seed train [. .. ] technology transfer to manufacturing partners. Develop and optimize downstream unit operations including centrifugation, filtration/ concentration (e. g. tangential flow filtration) , and lyophilization for LBP drug substance. Develop and characterize formulation intermediates and bulk drug substance presentations, including assessment of cryoprotectants, excipients, and storage conditions on organism stability. Plan and execute pilot stability studies for in-process intermediates and bulk drug substance; analyze and interpret data to establish in-process limits and bulk storage specifications. CDMO Vendor Coordination Serve as a [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Principal/ Senior Scientist, Biological Process Development
• München, Bayern
The Senior Scientist, Biological Process Development is a highly skilled and collaborative team member responsible for designing, executing, and interpreting experiments that advance
drug substance process development for the companys [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] live biotherapeutic product (LBP) pipeline. This role spans both upstream and downstream processing activities for drug substance-from fermentation optimization and scale-up through harvest, concentration, lyophilization, and preparation for drug product manufacturing. In addition to strong bench science capabilities, the Senior Scientist will play an active role in coordinating technical activities with external contract development and manufacturing organizations (CDMOs) and specialist vendors, serving as an informed day-to-day liaison between internal development programs and the external partner network. KEY RESPONSIBILITIES Process Development Design and execute fermentation development experiments using bench-top and pilot-scale bioreactors, including operation of anaerobic culture systems appropriate for LBP organisms. Optimize culture media, seed train [. .. ] technology transfer to manufacturing partners. Develop and optimize downstream unit operations including centrifugation, filtration/ concentration (e. g. tangential flow filtration) , and lyophilization for LBP drug substance. Develop and characterize formulation intermediates and bulk drug substance presentations, including assessment of cryoprotectants, excipients, and storage conditions on organism stability. Plan and execute pilot stability studies for in-process intermediates and bulk drug substance; analyze and interpret data to establish in-process limits and bulk storage specifications. Serve as a technical contact for [. .. ]
Job am 10.04.2026 bei Jobleads gefunden
• München, Bayern
Clotrimazole and also betamethasone cream is a mix
drug that is commonly made use of for the therapy of different skin conditions. This unique formula integrates the antifungal medicine clotrimazole [...]
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[...] with the corticosteroid betamethasone, supplying a twin activity for effective remedy for itching, inflammation, as well as infections. In this write-up, we will check out the usages, advantages, [. .. ] powerful anti-inflammatory buildings. It acts by suppressing the immune response and also reducing inflammation, providing relief from itching, swelling, and redness. As part of the clotrimazole and betamethasone cream formulation, betamethasone enhances clotrimazoles antifungal activity, offering an extensive treatment for different skin problem. By inhibiting the release of inflammatory mediators as well as minimizing the task of immune cells, betamethasone assists relieve the skin, relieving pain triggered by eczema, dermatitis, and other inflammatory skin conditions. It likewise aids in taking [. .. ] with the anti-inflammatory impacts of betamethasone, this cream provides relief from itching, inflammation, and fungal infections. It is important to utilize this lotion as routed by a health care specialist as well as to be familiar with prospective negative effects. Speak with a health care specialist for customized suggestions and support regarding making use of clotrimazole as well as betamethasone hanker your specific problem. #J-18808-Ljbffr 88028491 [. .. ]
Job vor 5 Tagen bei Neuvoo gefunden
Terumo
Job Summary As a QA Operations
Specialist, you ensure that daily operations across manufacturing, quality control, engineering and warehousing are fully compliant with GMP and internal procedures. You will act [...]
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[...] as a key QA partner on the shop floor, providing guidance, performing document reviews, and supporting quality events such as deviations, CAPAs and change controls. In addition, [. .. ] Support real-time batch review and preparation of batch documentation packages Ensure QA compliance during qualification and validation activities Perform cleanroom release activities for GMP manufacturing Oversee quality aspects of drug product manufacturing (formulation, aseptic filling, lyophilisation, inspection and packaging) Manage abnormal and rejected materials, including SAP handling (blocking/ unblocking, master data updates) Support deviations, CAPAs, change controls and other quality events Contribute to the review and improvement of SOPs, risk assessments and batch documentation Perform electronic data review ensuring data integrity and GMP [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
GULP experts united
• Biberach, Baden- Württemberg
Absolventen, Einsteiger, Trainees
Shape the future of
drug development with us In a dynamic and international environment, we bridge the gap between cutting-edge IT and pioneering science. We are seeking a dedicated individual [...]
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[...] to join our interdisciplinary team. This individual will manage complex IT systems in (non-) GMP environments, establish innovative digital tools, and act as [. .. ] innovative digital solutions in close coordination with users, including modern approaches to software development and the use of AI tools. As a process expert, you act as an interface between specialist departments, IT experts and external partners, driving continuous improvement. In addition, you will support scientists in analyzing complex data, thus making an important contribution to well-founded drug development decisions. Your profile Completed Masters degree in Computer Science, alternatively a completed Bachelors degree in Computer Science with several years of [. .. ] experience Proven experience with data structures, techniques for statistical data analysis, and expertise in current programming languages such as Python and R. Prior experience in pharmaceutical process knowledge, particularly in formulation development, process development, and GMP-compliant manufacturing and distribution of clinical trial samples, is advantageous. Strong teamwork skills and the ability to work agilely and in a goal-oriented manner in cross-functional teams. High social, communicative and methodological competence, combined with a structured, independent and solution-oriented work style. [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
Terumo
Job Summary The QA Operations
Specialist ensures that daily GMP operations are executed in compliance with internal procedures and global regulatory expectations. You will provide handson QA presence in [...]
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[...] manufacturing and warehouse areas, perform routine quality checks, support quality events, and manage material status in SAP. Your work in our CDMO plant in Leverkusen directly contributes [. .. ] documentation packages and perform realtime batch record review on the shop floor. Inspect and release cleanrooms for GMP manufacturing. Perform AQL assessments following visual inspection activities. Oversee GMP activities for drug product manufacturing, including formulation, aseptic filling, lyophilization, visual inspection, and packaging. Handle abnormal or rejected materials physically and in SAP, including blocking/ unblocking and maintaining material master data. Support Change Controls, Deviations, CAPAs, and other quality events. Review and revise SOPs, QRAs, and MBRs to drive continuous improvement. Perform electronic data review to ensure [. .. ]
Job am 15.04.2026 bei Neuvoo gefunden
Siegfried
• Hamelin, Lower Saxony
[. .. ] large scale to finished products. We integrate our offer seamlessly into the customers value chain. Our comprehensive services range from early-stage Research Development services such as synthesis, [...]
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[...] scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products. What we do in Hameln Hameln is a renowned contract manufacturer which supplies both national and international pharmaceutical companies. It has over 450 employees who produce sterile medicinal products, mainly for use in hospitals and intensive care facilities. Main activities Contract manufacture of parenteral solutions and suspensions aseptic or terminally sterilized in ampoules and vials Specialist in the production of complex preparations such as anesthetics, flammable and oxygen-sensitive liquids and cold chain products Special features Successful transfers and establishment of new products in sterile production Batch size: up to 3500 liters Clean room area: 4000 m Batch manufacture and filling of sterile products, from visual [. .. ]
Job am 15.04.2026 bei Neuvoo gefunden
Siegfried
• Hamelin, Lower Saxony
Abgeschlossenes Studium
[. .. ] large scale to finished products. We integrate our offer seamlessly into the customers value chain. Our comprehensive services range from early-stage Research Development services such as synthesis, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R D material for clinical trial purposes to commercial production. We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products. What we do in Hameln Hameln is a renowned contract manufacturer which supplies both national and international pharmaceutical companies. It has over 450 employees who produce sterile medicinal products, mainly for use in hospitals and intensive care facilities. Main activities Contract manufacture of parenteral solutions and suspensions aseptic or terminally sterilized in ampoules and vials Specialist in the production of complex preparations such as anesthetics, flammable and oxygen-sensitive liquids and cold chain products Special features Successful transfers and establishment of new products in sterile production Batch size: up to 3500 liters Clean room area: 4000 m Batch manufacture and filling of sterile products, from visual [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Drug Formulation Specialist pro Jahr?
Als Drug Formulation Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Drug Formulation Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 8 offene Stellenanzeigen für Drug Formulation Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Drug Formulation Specialist Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Drug Formulation Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Drug Formulation Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Drug Formulation Specialist Stellenangebote:
- Terumo (2 Jobs)
- Siegfried (2 Jobs)
- mbiomics GmbH (1 Job)
- GULP experts united (1 Job)
In welchen Bundesländern werden die meisten Drug Formulation Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Drug Formulation Specialist Jobs werden derzeit in Niedersachsen (2 Jobs), Bayern (2 Jobs) und Baden-Württemberg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Drug Formulation Specialist Jobs?
Drug Formulation Specialist Jobs gehören zum Berufsfeld Pharmazie.
