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Emploi Regulation district de Soleure SO

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Biogen  -  Soleure SO
 ...the Clean/GMP Utilities and align them with global procedures and guidelines. MAIN ACCOUNTABILITIES: 1. Analyzes Customers, Regulation and Biogen policies/SOP expectation for Clean/GMP Utilities and identify any gaps with our actual systems. Evaluate the risks correlated... 
il y a 15 jours
Biogen  -  Soleure SO
 ...Department in accordance with current guidelines on equipment, utilities, and facilities validation, in compliance with pertinent regulations (e.g., FDA, EMA). 2. Assesses overall validation workload, staffs accordingly, and deploys resources to attain Manufacturing... 
il y a 20 jours
Biogen  -  Soleure SO
 ...guidelines. MAIN ACCOUNTABILITIES: 1. Compiles updates and analyzes programs and data to ensure proper compliance with government regulations and to provide for a safe and healthy workplace, community and environment. 2. Oversees the development, implementation and... 
il y a 24 jours
Biogen  -  Soleure SO
 ...candidate holds a relevant degree combined with minimum 8 years of relevant management and operations experience and/or training in a GMP regulated industry, including: • Working knowledge of materials and supply chain management (ERP/MRP systems) • Strong knowledge in... 
il y a 7 jours
Biogen  -  Soleure SO
 ...into daily GMP operations. The Head of Quality has the overall responsibility to ensure the requirements of the Quality System Regulations is effectively established and maintained and is to ensure a Responsible Person for the Solothurn Site is appointed when... 
il y a 12 jours
Biogen  -  Soleure SO
 ...and operation knowledge within electrical installation and equipment. - Practical knowledge and application of GMP’s and EMEA regulations. - Experience in a pharmaceutical or biotech manufacturing environment. - Proficiency in MS Word, MS Excel, MS Power Point and... 
il y a 20 jours
Biogen  -  Soleure SO
 ...and clean utilities. - Demonstrated proficiency in Good Practice requirements (GMP, GEP) as well as biopharmaceutical industry regulations and norms as they relate to validation. - Strong technical writing and communication skills in English. German an advantage.... 
il y a 29 jours
Biogen  -  Soleure SO
 ...least 3 years of experience within Quality Assurance or related function is preferred - Maintain knowledge of relevant FDA/EMA regulations and compliance. - Prior experience with regulatory audits - Good communication skills in English, verbally and written. Dual... 
il y a 12 jours
Biogen  -  Soleure SO
 ...procedures and overall cGMP compliance. 3. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures all safety incidents are properly investigated and corrective / preventive actions are implemented. 4. Maintains the... 
il y a 26 jours
Biogen  -  Soleure SO
 ...Number 30805BR Qualifications The ideal candidate holds a relevant degree combined with solid, hands-on experience from a GMP regulated industry with complex production/operation. Team leader experience a plus. Education Minimum Bachelor’s degree (BS) in Chemical... 
il y a 22 jours
cBcon  -  Soleure SO
 ...procedures to assure consistent, efficient and compliant regulatory processes ~Support compliance activities related to global regulations and international standards; May assist in the performance of internal quality and regulatory compliance audits and the evaluation... 
Postuler sur Jooble Il y a 2 mois
Biogen  -  Soleure SO
 ...implementation of EHS procedures and programs required. - Advanced knowledge of EHS Management Systems, technical programs and swiss regulations required. - In-depth knowledge of drug development process with particular emphasis on large scale bioprocessing highly... 
il y a 12 jours
Biogen  -  Soleure SO
 ...control documents and activities associated with change control*LI-POT4 Qualifications- Maintain knowledge of relevant FDA/EMA regulations and compliance. - Approximately 4 years of experience in pharmaceutical or biotech manufacturing environment. - Previous experience... 
il y a 12 jours
Biogen  -  Soleure SO
 ...change control documents and activities associated with change control Qualifications - Maintain knowledge of relevant FDA/EMA regulations and compliance. - Maintain knowledge of GAMP and applicable automation regulatory knowledge - Approximately 10 years of experience... 
il y a 21 jours
Biogen  -  Soleure SO
 ...requiring director level approval. 3. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures all safety incidents are properly investigated and corrective / preventive actions are implemented. Support Technology... 
il y a 23 jours
Biogen  -  Soleure SO
 ...procedures and overall cGMP compliance. 3. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures all safety incidents are properly investigated and corrective / preventive actions are implemented. 4. Maintains the... 
il y a 26 jours
cBcon  -  Soleure SO
 ...data sets that support Technical File maintenance and sustainability Skills ~Profound knowledge of European Medical Device Regulations, especially Council Directive 93/42/EEC ~2-3 years of experience in European Medical device industry especially with regulatory,... 
Postuler sur Jooble Il y a 2 mois
Biogen  -  Soleure SO
 ...processes.*LI-DEN1 QualificationsThe ideal candidate holds a relevant degree combined with solid, hands-on experience from a GMP regulated industry with complex production/operation. Team leader experience a plus. EducationMinimum Bachelor’s degree (BS) in Chemical/Biochemical... 
il y a 22 jours
Biogen Idec International  -  Soleure SO
 ...procedures and overall cGMP compliance. 3. Creates and maintains systems that promote safety and comply with all safety procedures and regulations. Ensures all safety incidents are properly investigated and corrective / preventive actions are implemented. 4.Develop Capital... 
Il y a un mois
Suisse
 ...Experience with label UDI positioning and reading using DI and PI Other Skills: Expertise in ISO 13485, ISO 14971, FDA and EU regulations Needs to understand how to read and work with a project plan Needs to know how to build and work with workflow and... 
il y a 9 jours

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