Kaiseraugst, Aargau, Switzerland · On-site
We are looking for team players, who want to share their knowledge with our team and improve their personal capabilities Background in analytical chemistry/ biochemistry/ life science Experience in the analytical-pha…
Skills: Analytical Chemistry, Biochemistry, Life Science, Quality Assurance, GMP
Morrisville, North Carolina, United States · On-site
Position Overview Located at our large molecule headquarters in Research Triangle Park (RTP), North Carolina, the Senior Scientist position will be in the AC team supporting analytical activities related to large molecul…
Skills: UPLC, HPLC, CE-SDS, LC-MS, iciEF
Morrisville, North Carolina, United States · On-site
Position Overview Located at our large molecule headquarters in RTP, North Carolina, the Senior Scientist, Molecular Biology will be experienced and well versed in various molecular biology (MolBio) techniques related to…
Skills: qPCR, ddPCR, Next Generation Sequencing, Method Development, Method Validation
Morrisville, North Carolina, United States · On-site
Located at our US headquarters in RTP, North Carolina, the Scientist, Virology position will be experienced and well versed in various technical aspects related to viral and cell culture maintenance and viral quantificat…
Skills: Viral Culture, Cell Culture, Vector Design, Cell Line Development, Gene Editing
Morrisville, North Carolina, United States · On-site
Position Overview Located at our US headquarters in RTP, North Carolina, the Senior Scientist, Virology position will have expertise in key virology skills, including viral culture techniques, virus identification, virus…
Skills: Viral Culture Techniques, Virus Identification, Virus-Host Interaction Analysis, TCID50, rcAAV
Morrisville, North Carolina, United States · On-site
Located at our US headquarters in RTP, North Carolina, the Senior Analyst, Virology position will be experienced in basic laboratory techniques related to viral and cell culture maintenance and viral quantification metho…
Skills: Viral Culture Maintenance, Viral Quantification, Infectious Titer, rcAAV, RCL
Morrisville, North Carolina, United States · On-site
Position Overview Located at our large molecule headquarters in Research Triangle Park (RTP), North Carolina, the Senior Analyst/Analyst position will be one of the primary lab analysts for the CBBA team supporting CBBA …
Skills: ELISA, Cell Culture, Aseptic Techniques, Flow Cytometry, Cell Based Bioassay
Kaiseraugst, Aargau, Switzerland · On-site
Du möchtest etwas bewegen und Teil einer wachsenden Firma werden? In unserem Team Pharmacopeia Solutions übernimmst du eine vielseitige Rolle im Labor für physikalische und nasschemische Analysen. Du arbeitest in einem e…
Skills: Karl-Fischer Titration, Physical Analysis, Wet Chemical Analysis, GMP, English
Kaiseraugst, Aargau, Switzerland · On-site
The Chromeleon Method Template Specialist is responsible for the translation, modification, maintenance, and verification of Chromeleon methods and report templates during the upgrade from Chromeleon 7.2.10 to 7.3.2. Thi…
Skills: Chromeleon CDS, Method Configuration, Reporting, System Migrations, CSV
Kaiseraugst, Aargau, Switzerland · On-site
The Consolidation & Reporting Manager supports the finance organisation within a CRO environment and reports to the Head of Controlling, Reporting & Consolidation. As a key member of Group Finance, this role owns and exe…
Skills: Group Consolidation, Financial Reporting, Swiss GAAP FER, Tagetik, Microsoft Dynamics
Kaiseraugst, Aargau, Switzerland · On-site
The Lab IT Administrator is responsible for the day to day administration, support, and stability of laboratory IT systems and applications. The role ensures reliable operation of lab applications and infrastructure, pro…
Skills: IT Administration, Laboratory IT Support, GMP Regulations, Data Integrity, Chromeleon
Kaiseraugst, Aargau, Switzerland · On-site
The Senior LIMS and Service Delivery manager is a strategic leadership role responsible for the development, administration, support, governance, and continuous improvement of the Laboratory Information Management System…
Skills: LIMS Configuration, IT Service Management, Stakeholder Management, SDLC, Computer System Validation
Canton, Massachusetts, United States · On-site
Position Overview Responsible for performing analytical chemical analyses of test samples utilizing a variety of analytical techniques and instrumentation while conforming to appropriate regulatory requirements, includin…
Skills: HPLC/MS, DI-GC/MS, HS-GC/MS, Method Development, GLP
Canton, Massachusetts, United States · On-site
Position Overview This position requires both supervisory and technical experience. Responsible for overall project leadership and serves as point of contact for client consultation and technical review of studies. Requi…
Skills: Project Leadership, Technical Review, Method Validation, Regulatory Compliance, Supervision
Fort Lee, New Jersey, United States · Hybrid
The Commercial Support Specialist supports the North America Commercial organization by improving operational efficiency, streamlining sales processes, and enabling the sales team to focus on revenue-generating activitie…
Skills: Salesforce (SFDC), CRM Data Management, Commercial Operations, Sales Support, Contract Administration
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The QA Manager is responsible for leading projects across sites and ensuring compliance within a GMP environment. They will manage data integrity and computerized systems risk assessments while collaborating with cross-functional teams.
Candidates must have a background in analytical chemistry or life sciences and proven experience in the pharmaceutical QA environment. Proficiency in GMP regulatory frameworks (FDA, ICH, USP, Ph. Eur.) and fluency in English are required.
We are looking for team players, who want to share their knowledge with our team
and improve their personal capabilities
Background in analytical chemistry/ biochemistry/ life science
Experience in the analytical-pharmaceutical environment, preferably experience in
QA
Skills to solve the problems and build a good relationship with various stakeholders
Good interpersonal skills and team work spirit
Ability to collaborate in a dynamic, cross-functional matrix environment
Ability to lead projects between sites and work independently
Broad knowledge and proven experience of the regulatory framework in the GMP
environment (ICH, FDA, USP, Ph. Eur.)
Solid background in data integrity and computerized systems risk assessment and
project support
Experience as system administrator or deeper IT knowledge is an asset
Fluency in English and German as a plus is required
Solvias is a world leader in pharmaceutical CMC analysis (CRO).
Solvias helps innovative companies advance their path to commercialization with CMC analytical solutions powered by deep scientific expertise and a relentless focus on our customers’ success. With years of expertise in small molecules, biologics and cell and gene therapies, our talented subject matter experts have the know-how, creativity, and tenacity to solve even the most complex analytical challenges. Solvias offers comprehensive testing solutions from raw materials to final release testing as well as API development for small molecules. Customers have a single, trusted analytical partner for their entire development journey. Our six global facilities are strategically placed in biopharmaceutical hubs. We are GMP, GLP and ISO certified and conduct over 100 successful customer audits every year. We take pride in putting science and quality at the heart of everything we do, helping our customers bring better and safer products to market faster.
Offices: Römerpark 2, Kaiseraugst, Aargau 4303, CH · ZI rue du Canal d’Alsace, Hombourg, Haut-Rhin 68490, FR · 480 Neponset St, Building 7, Canton, Massachusetts 02021, US · 2400 Perimeter Park Dr, Morrisville, North Carolina 27560, US · Yalelaan 62, Utrecht, 3584 CM, NL
Solvias is a world leader in pharmaceutical CMC analysis (CRO).
Solvias helps innovative companies advance their path to commercialization with CMC analytical solutions powered by deep scientific expertise and a relentless focus on our customers’ success. With years of expertise in small molecules, biologics and cell and gene therapies, our talented subject matter experts have the know-how, creativity, and tenacity to solve even the most complex analytical challenges. Solvias offers comprehensive testing solutions from raw materials to final release testing as well as API development for small molecules. Customers have a single, trusted analytical partner for their entire development journey. Our six global facilities are strategically placed in biopharmaceutical hubs. We are GMP, GLP and ISO certified and conduct over 100 successful customer audits every year. We take pride in putting science and quality at the heart of everything we do, helping our customers bring better and safer products to market faster.
Offices: Römerpark 2, Kaiseraugst, Aargau 4303, CH · ZI rue du Canal d’Alsace, Hombourg, Haut-Rhin 68490, FR · 480 Neponset St, Building 7, Canton, Massachusetts 02021, US · 2400 Perimeter Park Dr, Morrisville, North Carolina 27560, US · Yalelaan 62, Utrecht, 3584 CM, NL
