Senior Scientist responsible for planning, allocation, and execution of analytical validation and quality assurance activities within the EGMP Analytical Development team.
Responsibilities
Planning and allocation of routine and non-routine activities for the team
Investigating QMS elements and generating reports
Coordinating with QA and other departments for QC functions
Interacting with clients and project teams
Reviewing in-process, cleaning, intermediate and finished product specifications
Requirements
M Sc / M Pharma (Analytical/General chemistry)
Nice to have: Chromeleon data management application
The Federal Account Executive is responsible for driving new business and expansion across U.S. federal customers – including the Department of Defense, Services, Intelligence Community, and federal civilian agencies.
Responsibilities
Build and execute account and capture strategies across DoD, IC, and federal civilian agencies
Identify and engage key stakeholders across program offices, engineering leadership, and contracting teams
Drive outbound prospecting aligned to mission priorities, budget cycles, and funded programs
Partner with Government Relations and Demand Gen to shape early demand and position Istari in emerging opportunities
Qualify opportunities based on mission alignment, technical feasibility, funding availability, and acquisition pathway
Requirements
Nice to have: Experience with major DoD branches or IC agencies
Nice to have: Experience transitioning programs from pilot to program of record
Nice to have: Familiarity with IL2–IL6 environments
Perform various analytical testing using chromatographic and wet chemistry techniques, execute method transfer and validation, document work for GMP compliance, and train technical staff.
Responsibilities
Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
Execute specialized analyses and method transfer and feasibility testing
Document work as required for GMP compliance
Perform tests accurately
Troubleshoot method and instrumentation problems
Requirements
Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration
Perform routine laboratory duties to ensure high-quality analytical chemistry services.
Compensation
Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons.
Responsibilities
Receive, examine, and record inbound items for testing
Deliver test samples to the sample staging area
Monitor supplies needed for testing and notify Laboratory Management
Prepare samples and quality control specimens, standardize reagents and solutions, calibrate equipment
Perform testing of samples and quality control specimens using specified methodology
Als Chemisch Analist in ons chemie laboratorium in de Botlek voer je zelfstandig een breed spectrum van chemische analyses uit op vloeibare (petro) chemicaliën en gassen.
Compensation
Een salaris dat past bij jouw kennis, ervaring en de verantwoordelijkheden van de functie.
Responsibilities
Voert kwantitatieve en kwalitatieve inspecties en analyses uit
Werkt met GC, IC, ICP, ICP-MS, AAS, UV-VIS, IR-spectometrie, Headspace-GC en diverse Nat-chemische technieken
Verantwoordelijk voor het hele proces van monster tot analyse
Werkt in dagdiensten in een klein en gezellig team
Provide analytical support to the client’s drug substance manufacturing and method development services, involving project analysis, method development, forced degradation studies and proof of concept method validation.
Responsibilities
Provide analytical support for Eurofins’ drug substance manufacturing and method development projects
Perform project analysis, method development activities, forced degradation studies, proof of concept validation work, and data interpretation
Contribute to the authoring and review of key analytical documentation
Work independently and collaboratively within a multidisciplinary team
Apply strong technical expertise and problem-solving skills to investigate challenges
We are seeking an innovative and highly motivated Analytical Development Scientist to join our R&D organization. In this role, you will contribute to the development and commercialization of next-generation analytical technologies with a primary focus on HPLC products and processes supporting critical to quality attributes in the biotechnology and biopharmaceutical industries.
Compensation
The salary range estimated for this position based in Massachusetts is $92,000.00–$135,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.
Responsibilities
Develop, optimize, and apply analytical HPLC methods to characterize product performance and support new product development.
Design and execute experiments to evaluate product attributes relevant to regulated bioprocessing, biologics development, and drug-quality monitoring.
Develop analytical strategies to assess critical-to-quality attributes, including purity, aggregation, charge variants, identity, concentration, or other relevant product and process attributes.
Generate, analyze, and interpret complex analytical datasets to guide technical decisions, product requirements, and development strategy.
Evaluate HPLC product performance across relevant use conditions, sample types, workflows, and customer applications.
Requirements
Ph.D. or M.S. with 3+ years of experience in Analytical Chemistry, Biochemistry, Chemical Engineering, Biotechnology, Pharmaceutical Sciences, or a related scientific field
Execute analytical techniques in support of method validation for Active Pharmaceutical Ingredient manufacturing.
Compensation
The full-time equivalent pay range for this position is $85,840.00 - $134,125.00/yr plus eligibility for bonus, stock and benefits.
Responsibilities
Design and conduct laboratory scale experiments using analytical instrument platforms such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, Karl Fischer
Author method validation protocols and reports with adherence to ICH guidelines and internal Agilent standard operating procedures (SOPs)
Design and safely conduct laboratory scale experiments using current best practices for API testing
Properly record and summarize experiments in notebooks and reports and construct research summaries to present to internal teams
Maintain process compliance integrity by adhering to SOPs and current good manufacturing practices (cGMP) as appropriate
Requirements
Bachelor's degree (B. S.) or equivalent in chemistry, or related applied science field
Nice to have: Experience with IC, GC, GC-MS, UV, Karl Fischer
Nice to have: Experience working in a cGMP regulated environment
Nice to have: Knowledge of analytical test methods used in the testing of oligonucleotide API or related molecules
Bachelor's with 5+ years of experience in Analytical Chemistry, Biochemistry, Chemical Engineering, Biotechnology, Pharmaceutical Sciences, or a related scientific field
Senior ScientistSyngene International Limited · Bangalore, India
Federal Account Executive (AE)Istari Digital · Remote, US
Laboratory Technician II - Analytical ChemistryIntertek · Houston, US