835 Jobs für Submissions
Stellenangebote Submissions Jobs
Job vor 9 Tagen bei StepStone gefunden
Milteny GmbH
• Bergisch Gladbach
Homeoffice möglich
[. .. ] amendments, and study-related documents fall within your scope of responsibility. A key focus lies in ensuring the generation of high-quality clinical data and supporting the preparation of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory submissions (e. g. , IND, CTA, BLA, MAA) . Close collaboration with cross-functional teams; including medical, regulatory, biometrics, operations, CMC, and safety; is essential, as is representing Clinical Development in internal and external settings. Next to this, you support the professional development of junior scientists and contribute to establishing team-[. .. ]
Job vor 9 Tagen bei StepStone gefunden
Milteny GmbH
Senior Project Manager-Drug Development (m f d)
• Bergisch Gladbach
Homeoffice möglich
[. .. ] , MSc, Pharm D, Ph D) is preferred. You bring proven experience in the pharmaceutical or biotech industry, with substantial involvement in global drug development programs; experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in planning and executing regulatory submissions (IND, BLA, MAA, etc. ) is a plus. You have a proven track record of managing complex cross-functional projects in a matrix environment, with strong project planning, timeline management, and organizational skills. You possess excellent written and verbal communication skills in English and are highly proficient in project management [. .. ]
Job vor 9 Tagen bei StepStone gefunden
Milteny GmbH
• Bergisch Gladbach
Führungs-/ Leitungspositionen Homeoffice möglich
[. .. ] medical writing and you are experienced in setting up standards and processes. You have a strong track record of authoring and managing key regulatory submission documents; experience [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with MAA/ BLA submissions is a plus. Experience with ATMPs/ CAR-T treatments, oncology/ hematology or autoimmune diseases is a plus. You demonstrate leadership through mentoring and managing small teams, ensuring high-quality deliverables. Your profile is rounded by a solid understanding of drug development and regulatory frameworks (ICH, EMA, FDA) , excellent project [. .. ]
Job am 02.12.2025 bei StepStone gefunden
Danaher
Trade Compliance Analyst II
• Dusseldorf
[. .. ] broker management oversight, KPI tracking, and QBR preparation to ensure operational efficiency and compliance. Coordinate and prepare export license applications and permits, including end-user screenings, Letters of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Indemnity, and submissions to authorities such as BAFA, CITES, and USDA. Manage trade data classification, country of origin, valuation, and recordkeeping to ensure accurate and timely customs clearance in accordance with applicable regulations. Conduct post-entry reviews, self-testing audits, and support government audit activities as required. Support Daily Management, KPI reporting, and [. .. ]
Job vor 4 Tagen bei Stellen-Online gefunden
Link Medical
• 10783, Berlin
Führungs-/ Leitungspositionen
[. .. ] a CRA role. As a CRA you may also be outsourced to clients, and the position will involve frequent travelling related to monitoring visits. Tasks Perform local [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical study application submissions in Germany mainly, but also in Austria and Switzerland. (This includes both medicinal products and medical device studies and interventional as well as non-interventional studies. ) Preparation and translation of submission documents (including ICFs) . Stay up to date about local regulatory requirements for drug/ device development/ clinical study [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Beckman Coulter- Diagnostics
Trade Compliance Analyst II
• Dusseldorf
[. .. ] broker management oversight, KPI tracking, and QBR preparation to ensure operational efficiency and compliance. Coordinate and prepare export license applications and permits, including end-user screenings, Letters of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Indemnity, and submissions to authorities such as BAFA, CITES, and USDA. Manage trade data classification, country of origin, valuation, and recordkeeping to ensure accurate and timely customs clearance in accordance with applicable regulations. Conduct post-entry reviews, self-testing audits, and support government audit activities as required. Support Daily Management, KPI reporting, and [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Sanofi EU
• Oberursel (Taunus)
[. .. ] dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility/ p/ lilip Reviews and approves c GMP or regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reports/ change controls/ protocols/ submissions and associated action plans in order to ensure regulatory and c GMP compliance/ p/ lilip Analyses complex regulatory issues and processes, supports to build regulatory strategic plans and applies own professional knowledge to identify key areas of risk to compliance with registered details/ p/ lilip Acts as a source of regulatory [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Sanofi EU
Regulatory Site Officer-all genders-Fixed-term contract until 26.02.2027
• Bad Homburg
[. .. ] dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility/ p/ lilip Reviews and approves c GMP or regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reports/ change controls/ protocols/ submissions and associated action plans in order to ensure regulatory and c GMP compliance/ p/ lilip Analyses complex regulatory issues and processes, supports to build regulatory strategic plans and applies own professional knowledge to identify key areas of risk to compliance with registered details/ p/ lilip Acts as a source of regulatory [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Link Medical
• Hoppegarten, BB
Führungs-/ Leitungspositionen
[. .. ] a CRA role. As a CRA you may also be outsourced to clients, and the position will involve frequent travelling related to monitoring visits. Tasks Perform local [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical study application submissions in Germany mainly, but also in Austria and Switzerland. (This includes both medicinal products and medical device studies and interventional as well as non-interventional studies. ) Preparation and translation of submission documents (including ICFs) . Stay up to date about local regulatory requirements for drug/ device development/ clinical study [. .. ]
Job vor 9 Tagen bei Mindmatch.ai gefunden
Sanofi EU
Regulatory Site Officer-all genders-Fixed-term contract until 26.02.2027
• Frankfurt am Main
[. .. ] and Controls) dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility Reviews and approves c GMP or regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reports/ change controls/ protocols/ submissions and associated action plans in order to ensure regulatory and c GMP compliance Analyses complex regulatory issues and processes, supports to build regulatory strategic plans and applies own professional knowledge to identify key areas of risk to compliance with registered details Acts as a source of regulatory expertise for others and [. .. ]
Job am 05.11.2025 bei Jobware gefunden
MED- EL Medical Electronics
• Innsbruck (Österreich)
Führungs-/ Leitungspositionen
[. .. ] supporting breakthrough innovations from concept to market Anticipate and adapt to evolving regulatory landscapes by monitoring changes in standards and regulations, and preparing the business for seamless [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] transitions Lead global submissions and approvals, with primary responsibility for regulatory filings in the EU, US, Canada, China, and additional markets as assigned Your Profile Bachelors degree or higher degree (University, FH) in Biomedical Engineering, Life Sciences, or a related field Proven experience in Regulatory Affairs within the Medtech industry, with a strong understanding [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Worldwide Clinical Trials
Regulatory Affairs Specialist
• berlin
[. .. ] Regulatory Affairs Department does at Worldwide Regulatory Affairs is pivotal in navigating the complex regulatory landscape, ensuring the success of diverse clinical trials. As subject matter experts, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the team leads submissions to regulatory authorities, coordinates with ethics committees across EMEA, Asia Pacific, and Latin America, and ensures compliance with evolving regulations. Their expertise drives the development and approval of innovative medical products, supports business development efforts, and offers strategic guidance on contract negotiations. They also mentor junior staff, review key documentation [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
BIP Career Site
• münchen, BY
[. .. ] are saved as Autodesk or Revit; Good knowledge in Dynamo; Close coordination with other stakeholders and BIM structures appointment main builder and their sub-contractor for shop drawings [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] review and submissions; Close coordination with the client and other stakeholders to update shop drawings for implementation team to execute the plan accordingly; Advanced MS Office Suite working knowledge; Fluent in German and English. Why Bip? People at the center of our culture Trust and collaboration, entrepreneurship and courage, meritocracy and development drive [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
Contract Specialist
• münchen, BY
[. .. ] encompasses all activities for the life cycle maintenance of projects. Assumes accountability on start-up deliverables including, but not limited to: Life Cycle maintenance regulatory activities (study maintenance [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and amendment submissions, oversight of communication to competent authorities/ ethics committees, import/ export license extensions) Oversight of delivery of executed amended clinical trial agreements and investigator budgets with investigator sites Overall SSU timelines following site activation. Including any realignment required due to amendment needs. Updates plans in accordance with Standard Operating Procedures and/[. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Fiserv
• bad homburg
[. .. ] race, color, religion, national origin, gender, gender identity, sexual orientation, age, disability, protected veteran status, or any other category protected by law. Note to agencies: Fiserv does [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not accept resume submissions from agencies outside of existing agreements. Please do not send resumes to Fiserv associates. Fiserv is not responsible for any fees associated with unsolicited resume submissions. Warning about fake job posts: Please be aware of fraudulent job postings that are not affiliated with Fiserv. Fraudulent job postings may be used [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Essence Investment AG
Qualified Person
• weimar, TH
[. .. ] Evaluate and resolve OOS/ OOT results in collaboration with laboratories. 5. Leadership Cross-Functional Collaboration-Provide pharmaceutical oversight across operations teams including QA, Manufacturing, Supply Chain, and RA. -Support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory submissions and updates. -Serve as the primary quality authority for internal and external stakeholders. Requirements-Eligibility as a Qualified Person under 14 AMG. -University degree in pharmacy or other accepted life sciences with QP recognition. -35 years of GMP experience in pharmaceuticals, ideally involving herbal medicinal products or medical cannabis. -Experience [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Essence Investment AG
• jena, TH
[. .. ] Evaluate and resolve OOS/ OOT results in collaboration with laboratories. 5. Leadership Cross-Functional Collaboration-Provide pharmaceutical oversight across operations teams including QA, Manufacturing, Supply Chain, and RA. -Support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory submissions and updates. -Serve as the primary quality authority for internal and external stakeholders. Requirements-Eligibility as a Qualified Person under 14 AMG. -University degree in pharmacy or other accepted life sciences with QP recognition. -35 years of GMP experience in pharmaceuticals, ideally involving herbal medicinal products or medical cannabis. -Experience [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Copenhagen Infrastructure Partners
Intern, Energy Transition Fund
• hamburg
[. .. ] please avoid having a photo in your CV. We commit to an inclusive recruitment process and equality for all applicants. Please be aware that we will not [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accept speculative CV submissions for any of our roles from recruitment agencies, and any unsolicited candidate submissions will be exempt from any payment expectations and ownership. ---Building value that matters Founded in 2012, Copenhagen Infrastructure Partners P/ S (CIP) today is the worlds largest dedicated fund manager within greenfield renewable energy investments [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Essence Investment AG
Qualified Person
• erfurt, TH
[. .. ] Evaluate and resolve OOS/ OOT results in collaboration with laboratories. 5. Leadership Cross-Functional Collaboration-Provide pharmaceutical oversight across operations teams including QA, Manufacturing, Supply Chain, and RA. -Support [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] regulatory submissions and updates. -Serve as the primary quality authority for internal and external stakeholders. Requirements-Eligibility as a Qualified Person under 14 AMG. -University degree in pharmacy or other accepted life sciences with QP recognition. -35 years of GMP experience in pharmaceuticals, ideally involving herbal medicinal products or medical cannabis. -Experience [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Infosys Consulting- Europe
Sr. Principal Consultant, Regulatory Strategy and Advisory
• münchen, BY
Beratungs-/ Consultingtätigkeiten
[. .. ] in Regulatory and Clinical area with ability to drive futuristic IT solutions and experience in client facing and agency thought leadership. Understanding and knowledge of processes related [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to health authority submissions, content authoring, labeling, lifecycle management of CMC, regulatory intelligence, and country-specific regulatory requirements keenly aware of industry trends, needs and business requirements expected from clients Able to strategize and advise on the product roadmap and should work closely with the client in delivering solutions. An empathic people manager responsible [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Destinus
Bid Specialist
• münchen, BY
[. .. ] crafting sharp proposals, understanding regulations, and navigating public procurement will directly influence how our drone technologies are adopted across Europe. If you love mixing storytelling, strategy, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] compliance into powerful submissions, this is your arena. At Destinus, we are revolutionizing the defense industry with cutting-edge Unmanned Aerial Vehicles (UAVs) . Our innovative technologies are designed to meet the unique demands of modern defense operations, delivering unparalleled speed, precision, and cost effectiveness. Destinus partners with government agencies and defense organizations worldwide [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Siemens Healthineers
Senior Auditor
• erlangen, BY
[. .. ] get started. To all recruitment agencies: Siemens Healthineers recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] us. Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees. We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices. Your adherence to our policies is appreciated. Siemens Healthineers Germany was awarded the Great Place to Work certificate. 72831348 [. .. ]
Job vor 4 Tagen bei JobMESH gefunden
Link Medical
Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) / (Sr) CRA at LINK Medical (DE)
• State of Berlin 10783
Führungs-/ Leitungspositionen
[. .. ] a CRA role. As a CRA you may also be outsourced to clients, and the position will involve frequent travelling related to monitoring visits. Tasks Perform local [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical study application submissions in Germany mainly, but also in Austria and Switzerland. (This includes both medicinal products and medical device studies and interventional as well as non-interventional studies. ) Preparation and translation of submission documents (including ICFs) . Stay up to date about local regulatory requirements for drug/ device development/ clinical study [. .. ]
Job vor 9 Tagen bei JobMESH gefunden
Sanofi EU
Regulatory Site Officer-all genders-Fixed-term contract until 26.02.2027
• Germany
[. .. ] and Controls) dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility Reviews and approves c GMP or regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reports/ change controls/ protocols/ submissions and associated action plans in order to ensure regulatory and c GMP compliance Analyses complex regulatory issues and processes, supports to build regulatory strategic plans and applies own professional knowledge to identify key areas of risk to compliance with registered details Acts as a source of regulatory expertise for others and [. .. ]
Job vor 9 Tagen bei JobMESH gefunden
Sanofi EU
Regulatory Site Officer-all genders-Fixed-term contract until 26.02.2027
• Hesse Oberursel (Taunus)
[. .. ] dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility/ p/ lilip Reviews and approves c GMP or regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] reports/ change controls/ protocols/ submissions and associated action plans in order to ensure regulatory and c GMP compliance/ p/ lilip Analyses complex regulatory issues and processes, supports to build regulatory strategic plans and applies own professional knowledge to identify key areas of risk to compliance with registered details/ p/ lilip Acts as a source of regulatory [. .. ]
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Häufig gestellte Fragen
Wieviele offene Stellenangebote gibt es für Submissions Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 835 offene Stellenanzeigen für Submissions Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Submissions Jobs?
Aktuell suchen 89 Unternehmen nach Bewerbern für Submissions Jobs.
Welche Unternehmen suchen nach Bewerbern für Submissions Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Submissions Stellenangebote:
- Link Medical (14 Jobs)
- Freshfields Bruckhaus Deringer (14 Jobs)
- University of Maryland Global Campus (12 Jobs)
- Cpl Life Sciences (12 Jobs)
- Sanofi EU (11 Jobs)
- Cytel (11 Jobs)
In welchen Bundesländern werden die meisten Submissions Jobs angeboten?
Die meisten Stellenanzeigen für Submissions Jobs werden derzeit in Bayern (161 Jobs), Nordrhein-Westfalen (80 Jobs) und Berlin (79 Jobs) angeboten.
