129 Jobs für Pharmaceutical Writing
Stellenangebote Pharmaceutical Writing Jobs
Job vor 2 Tagen bei StepStone gefunden
Kintiga
• Hannover
Homeoffice möglich
[. .. ] knowledge sharing, internal capability building, mentoring, and cultural development Profil Masters degree in life sciences, medicine, pharmacy, health economics, or a related field 13 years of professional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] experience in the pharmaceutical industry and/or market access or management consulting Good knowledge of the German healthcare system and the AMNOG process, including experience with benefit dossiers Strong skills in scientific literature research and medical writing Experience in project management, as well as conducting and moderating trainings and workshops Native level German and excellent English language skills (C2) , both written and spoken Strong analytical, structured, and detailoriented working style with a high level of independence and reliability Confident communication and presentation skills, including the ability [. .. ]
Job vor 4 Tagen bei StepStone gefunden
HMNC Holding GmbH
Senior Clinical Pharmacologist (m/w/d)
• München Muenchen
Homeoffice möglich
[. .. ] who are not helped sufficiently by existing mental health therapies. The Company is headquartered in Munich, Germany. Aufgaben We are seeking a senior Clinical Pharmacology expert who [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. The successful candidate should not only understand clinical pharmacology, DMPK, Pop PK, PBPK, PK/ PD, ADME, and safety data, but also be able to interpret these data critically and translate them into clear development decisions. This person will act as a [. .. ] particularly valuable. Ability to think from both perspectives: the pharmaceutical sponsors need for efficient and feasible development and the authoritys need for robust scientific justification and patient safety. Strong scientific writing, communication, and stakeholder-management skills, with the ability to explain complex clinical pharmacology and DMPK topics clearly to cross-functional teams and senior decision-makers. Pragmatic, hands-on, and solution-oriented working style suitable for a small biotech environment, with the confidence to challenge assumptions and recommend practical solutions. Experience [. .. ]
Job vor 3 Tagen bei Neuvoo.com gefunden
CSL Behring
• Hessen
Führungs-/ Leitungspositionen
[. .. ] Projects. Accountable for ensuring that all Manufacturing Processes on site remain in a Validated State, including Cleaning Processes. Responsible for providing adequate Staffing for routine/ regularly recurring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Validation activities Oversees writing and reviewing of documents for required registrations and providing adequate responses to regulators regarding validation topics. Responsible for leading and performing Process Risk Assessments for the Site Manufacturing Processes using defined Risk Management tools. Responsible for providing input to Deviations related to Validation activities: support of the root cause analysis [. .. ] Requirements 1 Education Undergraduate/ graduate degree in Engineering or related technical field 2 Experience Required 10+ years working in Engineering, Process Development, or Validation of biopharmaceutical products and processes in Pharmaceutical, Chemical Manufacturing or similar industry. Demonstrated experience in process monitoring, analytics, and improvement development execution. Strong communication, negotiation, and conflict management skills to influence technical experts and stakeholders including non-specialists, at all levels in the organization. Demonstrated experience in managing, organizing, developing, and deploying best practice frameworks, processes, tools, [. .. ]
Job gestern bei Jooble gefunden
mbiomics GmbH
Principal/ Senior Scientist, Biological Process Development
• München
[. .. ] aligned and on schedule. Contribute to a culture of scientific rigor, continuous improvement, and open knowledge sharing across the company. QUALIFICATIONS Required Ph. D. in Microbiology, Biochemical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Engineering, Bioprocess Engineering, Pharmaceutical Sciences, or a closely related discipline with 3+ years of industry experience. Demonstrated hands-on expertise in microbial upstream process development, including bioreactor operation, media optimization, and process parameter characterization at bench and/or pilot scale. Practical experience in downstream processing of microbial products, including centrifugation, filtration, TFF, concentration, and bulk formulation. Strong scientific writing skills; experience authoring process development reports, SOPs. Preferred Experience working with anaerobic organisms, spore-forming bacteria, or other fastidious microorganisms in a development or GMP-adjacent setting is strongly preferred. Prior experience at a live biotherapeutics, microbiome therapeutics, or cell-based medicine company. Familiarity with lyophilization as it relates to [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Teleflex
• AT- 9 Wien
Homeoffice möglich
[. .. ] degree in life sciences, nursing or other health related disciplines or a comparable qualification. Minimum two years of onsite monitoring research experience as a CRA in the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] medical device or pharmaceutical industry or with a CRO. High level of attention to detail and strong organizational ability paired with excellent people skills. Excellent clinical trial monitoring skills. Previous knowledge of Vascular Interventional Cardiology and/or Peripheral Vascular Intervention is an advantage. Specialized Skills/ Other Requirements Strong working knowledge, understanding and ability to [. .. ] attention to detail and accuracy. Experience working independently in a regional area with remote or minimal supervision. Proficient knowledge of medical terminology. Effective time management and organizational skills. Excellent professional writing and oral communication skills. Excellent interpersonal skills. Experience with spreadsheets and database applications (e. g. , MS Word and Excel) . Ability to work independently within Teleflex systems. Ability to work independently and as part of a team. Responsible for adequate and reasonable home office set up including dedicated desk [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
Takeda
Head of Oral Drug Products (Vice President)
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] Executive leadership presence and confidence. Enterprise level leadership with the ability to inspire, motivate and drive results. Excellent communicator, able to persuasively convey both ideas and data, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] verbally and in writing. Ability to assemble and manage a diverse and high performing team. Demonstrated ability to lead teams across functions, regions and cultures. Ability to distill complex issues and ideas down to simple comprehensibility. Proven skills as leader who can engender credibility and confidence within and outside the company. Embraces and demonstrates [. .. ] negotiations with the ability to resolve conflict in a constructive manner. Ability to build strong partnerships and drive role clarity with other interfacing Takeda functions, including but not limited to Pharmaceutical Sciences, GSQ, GPLS, and Regulatory CMC. Innovation Visionary and forward thinking with the ability to influence and effectively drive organizational change and continuous innovation. Comfortable challenging the status quo and bringing forward innovative solutions. Ability to take risks implementing innovative solutions, accelerating time to market. EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS [. .. ]
Job am 03.06.2026 bei Jobleads gefunden
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] satisfaction Ensuring clear communication throughout projects and within the team Supporting the development of intellectual property for use on future engagements Developing broader and deeper knowledge of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] consulting methodologies and pharmaceutical market through on the job experience and training Providing direction, advice and intellectual leadership to clients and delivery teams. Direct consulting teams through consistent participation in team meetings Providing high level input to, and ensuring the development of, client reports and presentations and delivery of all or significant portions of [. .. ] sciences industries Minimum of 1+ years project management experience focused on multinational strategic consulting projects Welldeveloped written and verbal communication skills including presentations, chairing meetings, workshop facilitation, business and report writing Strong capability in managing large and/or multiple projects and juggling priorities so that deadlines are met while retaining consistently highquality outcomes Experience working in sizable/ multidisciplined teams and leading staff Experience in developing credible relationships with senior level managers and executives in the pharmaceutical/ healthcare industry Excellent interpersonal skills [. .. ]
Job am 03.06.2026 bei Jobleads gefunden
Senior/ Principal Pharmacovigilance Consultant
• München, Bayern
Beratungs-/ Consultingtätigkeiten
[. .. ] and experience in leadership and management. The company has recently expanded to include affiliates based in Germany and the US. Our growing team comprises over 90 qualified [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] professionals with a pharmaceutical and/or regulatory background, as well as over 30 dedicated supporting staff in areas of Business Development, Finance, Business Services and People Practices. We provide services to over 130 organisations, enabling them to achieve their strategic and operational development objectives. DLRCs expertise and flexible working approach ensures the provision of [. .. ] named Sponsor pharmacovigilance contact and escalate PV issues where appropriate. Provide oversight of pharmacovigilance vendors and third-party providers. Act as PV contact person for audits and inspections. Support the writing, review, and maintenance of pharmacovigilance system documentation, including: Pharmacovigilance System Master File (PSMF) Pharmacovigilance procedures and agreements Client-specific PV Standard Operating Procedures Attend safety review meetings as required. Provide the DLRC QPPV with the necessary information to fulfill their responsibilities. Ensure ongoing compliance with EU and UK pharmacovigilance legislation [. .. ]
Job am 24.04.2026 bei Jobleads gefunden
• Wien
Führungs-/ Leitungspositionen
[. .. ] Executive leadership presence and confidence. Enterprise level leadership with the ability to inspire, motivate and drive results. Excellent communicator, able to persuasively convey both ideas and data, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] verbally and in writing. Ability to assemble and manage a diverse and high performing team. Demonstrated ability to lead teams across functions, regions and cultures. Ability to distill complex issues and ideas down to simple comprehensibility. Proven skills as leader who can engender credibility and confidence within and outside the company. Embraces and demonstrates [. .. ] negotiations with the ability to resolve conflict in a constructive manner. Ability to build strong partnerships and drive role clarity with other interfacing Takeda functions, including but not limited to Pharmaceutical Sciences, GSQ, GPLS, and Regulatory CMC. Innovation Visionary and forward thinking with the ability to influence and effectively drive organizational change and continuous innovation. Comfortable challenging the status quo and bringing forward innovative solutions. Ability to take risks implementing innovative solutions, accelerating time to market. EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS [. .. ]
Neu Job vor 3 Std. bei Jobleads gefunden
Technical Process Excellence Lead OSD Manufacturing
• Neuenburg
Führungs-/ Leitungspositionen
We are recruiting a Technical Process Excellence Lead OSD Manufacturing for a world-renowned
pharmaceutical company. Technical Process Excellence Lead OSD Manufacturing-Temporary position Duration :: 6 months Main mission: Provides [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] technical leadership to ensure robust, compliant and efficient manufacturing processes. Responsible for complex documentation, the life cycle of equipment and expert in processes, MES and data integrity. Contributes to operational excellence through the field, [. .. ] Bachelors degree (or equivalent) in engineering or life sciences Experience of 3 to 5 years in a GMP environment, ideally in technical operations Strong knowledge of validation and technical documentation writing Proficiency in French required, good level of English #J-18808-Ljbffr 96437537 [. .. ]
Job gestern bei Jobleads gefunden
• Bulle, Freiburg
Führungs-/ Leitungspositionen
[. .. ] or equivalent in a scientific or technical discipline. Minimum 5 years of experience in a GM Pregulated environment, ideally within Quality Assurance or operations. Strong knowledge of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] GMPs and the pharmaceutical industry. Experience writing scientific/ technical documentation. Autonomous and strong at multitasking. Excellent communication (written verbal) . Strong project coordination and ability to meet critical deadlines. High discretion and attention to detail. Deep understanding of Gx P environment. Very strong meeting preparation and presentation skills. Strong negotiation and influencing capabilities. Proactive mindset, with a focus [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Senior Clinical Pharmacologist (m/w/d)
• München, Bayern
Job Summary We are seeking a senior Clinical Pharmacology expert who can combine deep
pharmaceutical industry experience with a strong understanding of regulatory authority expectations. The successful candidate should [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] not only understand clinical pharmacology, DMPK, Pop PK, PBPK, PK/ PD, ADME, and safety data, but also be able to interpret these data critically and translate them into clear development decisions. This person will act as a [. .. ] particularly valuable. Ability to think from both perspectives: the pharmaceutical sponsors need for efficient and feasible development and the authoritys need for robust scientific justification and patient safety. Strong scientific writing, communication, and stakeholdermanagement skills, with the ability to explain complex clinical pharmacology and DMPK topics clearly to crossfunctional teams and senior decisionmakers. Pragmatic, handson, and solutionoriented working style suitable for a small biotech environment, with the confidence to challenge assumptions and recommend practical solutions. Experience managing or guiding external CROs, [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Bayern
Führungs-/ Leitungspositionen
[. .. ] Lead and execute analytical transfer projects (setting up and execution of transfer plans, resource needs, and timeline adherences) for both drug substance and drug products Organize analytical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities in a pharmaceutical GMP and Quality Control (QC) environment Coordinate and mentor ATS (Analytical tech solutions) colleagues remotely to ensure governance of several Monoclonal Antibody projects Collaborate with R-D, Quality, Regulatory Affairs, external suppliers and division site responsible teams in transfer activities Support strategic transfer initiatives like standardizing transfer processes and develop [. .. ] approach Solid experience working in international project teams Ability to work independently and make decisions within guidelines and policies that impact own priorities to meet deadlines Proficient in scientific/ technical writing and current computer usage Required Skills Adaptability, Aseptic Processing, Assay, Biochemical Analysis, Chemometrics, Chromatography, Cross-Cultural Awareness, Cross-Functional Collaboration, Driving Continuous Improvement, Freeze Drying, GMP Compliance, Immunoassays, Lean Six Sigma Process Improvement, Manufacturing Quality Control, Monoclonal Antibodies, Pharmaceutical Microbiology, Process Improvements, Regulatory Compliance, Risk Management. Be part of a [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Senior Principal Scientist-Drug Metabolism and Pharmacokinetics (m/f/d)
• Wülfrath, Nordrhein- Westfalen Wuelfrath
[. .. ] direction based on scientific evidence Mentor junior scientists and contribute to the development of best practices in assay development and biotransformation studies WHO YOU ARE Ph. D. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Biology, Chemistry, Pharmaceutical Sciences, or a related field Extensive experience in DMPK, with a focus on assay development in biotransformation, particularly metabolite identification from in vitro and in vivo studies; long-term experience in the pharmaceutical industry preferred Strong experience in high-resolution mass spectrometry and analytics A solid background in drug discovery [. .. ] working collaboratively across departments Ability to manage multiple projects and priorities in a fast-paced environment Knowledge of relevant methodologies and technologies for biotransformation studies English fluent; verbally and in writing WHY BAYER? Our benefits package is flexible, appreciative, and tailored to your lifestyle, because: What matters to you, matters to us We ensure your financial stability through a competitive compensation package, consisting of an attractive base pay and our annual bonus. Whether its hybrid work models or part-time arrangements: [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
[. .. ] to build digital fluency, innovate responsibly, learn continuously, and collaborate across functions. Key responsibilities Independently managing key tasks for projects (e. g. release, stability studies, validation, and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] transfer activities) . Writing protocols, scientific reports, lab procedures and providing ready-to-submit documents intended for submissions (e. g. release or stability documents, transfer reports) . Approving GMP documents and test records as well as investigating quality events within the project (e. g. deviations, changes, out-of-specifications events) . Supporting the lab [. .. ] engineering, biology, chemistry, biochemistry or similar with at least 4 years strong relevant industry experience or Ph D in relevant field or equivalent and 2+ years of work experience within the pharmaceutical industry. Proficiency in English and German is beneficial. Good knowledge of sound technical scientific of pharmaceutical, chemical analytics, QC or equivalent. Proven experience within GMP environment. Good theoretical and scientific knowledge in the area of expertise (like HPLC, CE) . Desirable Requirements A personality with a can-do mindset and [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Senior Process Engineer (m/f/d)
• Bad Homburg vor der Höhe, Hessen
[. .. ] activities and ensure assigned laboratory and pilotplant equipment is maintained, calibrated and operated in line with quality and safety standards. Qualifications Masters degree in Chemical Engineering, Food [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Technology, Process or Pharmaceutical Engineering, Nutritional Science or a related discipline; a relevant Ph D is highly preferred. At least 6 years of relevant R D or product development experience in a regulated nutrition, lifescience, medical or clinical nutrition, FSMP, pharmaceutical or specialized food environment; candidates with a relevant Ph D should bring at least 3 [. .. ] simulation or microscopy considered an advantage. Proven experience in leading innovation or development projects, including feasibility studies, process scaleup and technology transfer in crossfunctional settings. Strong analytical, communication and technical writing skills, a proactive problemsolving mindset, and fluency in English and German; experience with MS Office and data analysis tools such as Origin or Minitab is an advantage. #J-18808-Ljbffr 96201887 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Neuenburg
We are recruiting a Technical Process Excellence Lead-OSD Manufacturing for a world-renowned
pharmaceutical company. Start date : ASAP Duration :: 6 months Main mission Provides technical leadership to ensure [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] robust, compliant and efficient manufacturing processes. Responsible for complex documentation, the life cycle of equipment and expert in processes, MES and data integrity. Contributes to operational excellence through the field, cross-functional collaboration, continuous [. .. ] Bachelors degree (or equivalent) in engineering or life sciences Experience of 3 to 5 years in a GMP environment, ideally in technical operations Strong knowledge of validation and technical documentation writing Proficiency in French required, good level of English #J-18808-Ljbffr 96189659 [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Process Expert (m/f/d) - Schaftenau, Tirol
Summary As a Process Expert, you will play a key role in ensuring the reliable, compliant, and efficient execution of aseptic filling processes within a highly regulated
pharmaceutical environment. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] About The Role Main Responsibilities Ensure business continuity for aseptic syringefilling operations by providing expert process support. Handle deviations endtoend, ensuring timely investigation, documentation, and release of batches. Develop, own, and continuously improve processes, including writing and optimizing process documentation. Create and maintain lifecycle documents to ensure compliance, accuracy, and inspection readiness. Represent the company as a Subject Matter Expert (SME) during Health Authority (HA) inspections. Collaborate with crossfunctional departments and manage stakeholders to align expectations and resolve issues efficiently. Participate in validation and qualification activities, [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] new treatments Presenting your work on international conferences and creating scientific publications YOUR PROFILE Motivated physician with at least 3 years experience in clinical research and development, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] preferably in the pharmaceutical industry Team player, able to act as a leader for medical and scientific contents High level of independent work and ability to assume global responsibility Fluent in English language with excellent scientific writing skills Innovative, solution-oriented, out of the box way of thinking High quality standards and ability to foster those in our development projects Excellent communication skills Ability to overcome hurdles and handle problems in a pragmatic and constructive way YOUR BENEFITS You will continuously develop your distinctive expertise and broaden [. .. ]
Job vor 4 Tagen bei Jobleads gefunden
Director Commercial Excellence Germany Austria
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] fast paced and growing business and deliver quick wins as well as future vision and roadmaps. Interacts effectively with cross-functional stakeholders on multiple levels. Fluent in English, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] both in writing and verbal Why Join Alfasigma At Alfasigma, we foster a culture where the courage to innovate is key to our success. We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development. Our commitment to people and patients is at the heart of everything we do. [. .. ] collaboration, and a shared passion for innovation are essential to achieving meaningful progress. Join Alfasigma and become part of a forward-thinking team dedicated to shaping the future of the pharmaceutical industry. #J-18808-Ljbffr 96101532 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Process Engineer (m/f/d)
• Bad Homburg vor der Höhe, Hessen
[. .. ] and ensure assigned laboratory and pilotplant equipment is maintained, calibrated and operated in line with quality and safety standards. Your Qualifications Masters degree in Chemical Engineering, Food [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Technology, Process or Pharmaceutical Engineering, Nutritional Science or a related discipline; a relevant Ph D is highly preferred. At least 6 years of relevant R D or product development experience in a regulated nutrition, lifescience, medical or clinical nutrition, FSMP, pharmaceutical or specialized food environment; candidates with a relevant Ph D should bring at least 3 [. .. ] simulation or microscopy considered an advantage. Proven experience in leading innovation or development projects, including feasibility studies, process scaleup and technology transfer in crossfunctional settings. Strong analytical, communication and technical writing skills, a proactive problemsolving mindset, and fluency in English and German; experience with MS Office and data analysis tools such as Origin or Minitab is an advantage. Ready To Make An Impact? If you are ready to combine scientific curiosity with handson process engineering and contribute to meaningful innovation in [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Design Quality Engineer II
• Aachen, Nordrhein- Westfalen
[. .. ] in an engineering or scientific discipline; an advanced degree is an asset. 1+ years of work experience in a highly regulated industry or equivalent Masters degree; medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] device and/or pharmaceutical industry preferred. Good communication skills, both verbal and written, in English and German. Experience conducting Process/ Design Failure Mode Effects and Analysis is an asset. Design control or new product development experience preferred. Experience supporting or conducting Process Verification/ Validation activities preferred. Experience with blueprint reading/ literacy including GD T [. .. ] Continuous Improvement, Database Backup, Data Savvy, Disruptive Innovations, Issue Escalation, Problem Solving, Process Oriented, Product Improvements, Quality Control (QC) , Quality Management Systems (QMS) , Quality Standards, Regulatory Environment, Report Writing. #J-18808-Ljbffr 95889079 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Senior Analytical Scientist-Biologics Evidence Lab (all genders)
• Esslingen am Neckar, Baden- Württemberg
[. .. ] results. You are familiar with GMP/ Gx P environments, including data integrity principles, SOPs, change control processes, deviations, and ICH-style approaches to analytical development and validation. You [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] demonstrate excellent scientific writing skills in English. You hold a degree in analytical chemistry, biochemistry, biotechnology, pharmaceutical sciences, biophysics, or a related field; a Ph D is preferred, though an MSc with strong and relevant industry experience is equally valued. Nice to have: Experience with MIR/ FTIR, NIR, Raman, UV-Vis, CD, fluorescence or other spectroscopic techniques. Experience with chemometrics or multivariate analysis, such as PCA, PLS, calibration, [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Clinical Consultant Biosurgery (m/w/d) Region Region Bayern (Bamberg-Hof-Regensburg-Sch. . .
Beratungs-/ Consultingtätigkeiten
[. .. ] product innovations especially for focus customers. Report and perform regular territory analysis, analysing customer profiles, developing and implementing sales and action plans in collaboration with the sales [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] manager. Qualifications Certified pharmaceutical sales representative or equivalent qualification in accordance with 75 AMG. Preferable: sales experience ideally in a clinical environment or training in the operatingroom or medical technology, experience in medical sales for haemostatics. Competent use of IT tools, especially Microsoft Office. Communicative, decisive, authentic personality. Reliable, responsible, teamoriented, selforganized and structured working style with strong organisational talent. Highly motivated, selfmotivated and outcomeoriented; creative and changeready; persuasive communication; flexibility and willingness for travel and conferences. Fluent German language skills in writing and speaking; basic English knowledge is beneficial. Benefits Competitive remuneration package including a flexible commission model, company car with unlimited personal use, pension plan, annual bonus, paid holidays, parental leave of at least 12weeks, bereavement and caregiving leave, volunteer leave, wellness reimbursement, financial, physical and mental health programmes, and defined [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Process Engineer Medical Devices
• Baden- Württemberg
[. .. ] since the 1960s. We continue to drive innovation in selfinjection pens, covering everything from design and manufacturing to packaging and delivery. We have developed solutions in scalable [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] volumes for numerous pharmaceutical partners always applying stateoftheart engineering practices and we aim to evolve further. We develop our products using a patientcentric approach. Our injection devices are used across various therapeutic areas, helping patients with diabetes, supporting fertility treatments, and even offering an option for gentle cancer therapy. Responsibilities Manage and coordinate the [. .. ] in process development or design transfer of medical devices CAD skills (Solid Works) to design tooling, fixtures, and processrelated components Good understanding of designformanufacturing and designforassembly (DFm/DFA) principles Experience writing technical documentation and reports of medical devices Proficient in English, German skills are desirable Being available for occasional travel to our suppliers or our production facility in Czech Republic Nice To Have Experience with qualification activities (IQ, OQ, PQ) and related documentation Experience or knowledge in 3D printing technologies (FDM [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Writing pro Jahr?
Als Pharmaceutical Writing verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Writing Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 129 offene Stellenanzeigen für Pharmaceutical Writing Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Jobs?
Aktuell suchen 38 Unternehmen nach Bewerbern für Pharmaceutical Writing Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Writing Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Writing Stellenangebote:
- West Pharmaceutical Services (3 Jobs)
- CSL Behring (2 Jobs)
- Simon- Kucher Partners (2 Jobs)
- PAION Pharma GmbH (2 Jobs)
- PM Group (2 Jobs)
- Kintiga (1 Job)
In welchen Bundesländern werden die meisten Pharmaceutical Writing Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Writing Jobs werden derzeit in Bayern (22 Jobs), Sachsen-Anhalt (15 Jobs) und Hessen (15 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Writing Jobs?
Pharmaceutical Writing Jobs gehören zum Berufsfeld Technische Dokumentation / Redaktion.
