Associate Scientist - Analytical
About The Position
Avantor is looking for a dedicated Associate Scientist to optimize our Biopharma / R&D organization. This person will be a member of a multi-disciplinary team of scientists focused on the development of new products. They will work under supervision, in cross-functional teams, to address analytical challenges by using various analytical methodologies to define product quality, evaluate impurities profile and establish product specifications. The successful applicant will have a broad background in the chemical sciences, hands-on experience, knowledge of wet chemistry/organic chemistry analytical techniques, and be curious to learn and adopt new skills. This is a full-time position onsite at our Bridgewater, NJ location.
Requirements
- MSc degree with 3+ years of industrial hands-on experience performing analytical method development, product/process development/characterization and technical problem-solving activities preferred.
- BSc degree with 5+ years of relevant hands-on experience performing analytical method.
- Hands-on experience and knowledge with analytical techniques used in test method validation such as: HPLC/UPLC, GC-FID, GC-MS; Wet chemistry analytical techniques.
- Strong competency in Microsoft Office, specifically PowerPoint, Word and Excel, Minitab,
- Excellent computer skills; ability to learn new systems (e.g. salesforce.com).
Nice To Haves
- Hands-on knowledge of Empower, MassLynx, ChemStation, OpenLab and Mass Hunter Software is considered a plus.
Responsibilities
- Conduct hands-on analytical testing needed for product characterization, process optimization and product commercialization under the supervision of a Research Scientist.
- Interface with project teams to support projects objectives and assist in resolving customer complaints related to product/process performance issues.
- Support the development, validation and transfer of analytical methods to internal and external QC laboratories for cGMP/Compendia finished goods release testing and stability studies/shelf-life determination.
- Maintain knowledge of cGMP, Compendia, FDA, ICH and other regulatory agency requirements.
- Participate in regular project check-in meetings and adjusts plan/activities based on feedback to meet project deadlines.
- Comply with all safety, environmental and quality policies, and procedures.
- Prepare reports, and data for publications and oral presentations to advance projects or resolve process/product issues and customer complaints.
Benefits
- medical coverage
- dental coverage
- vision coverage
- wellness programs
- health savings accounts
- flexible spending accounts
- 401(k) plan with company match
- employee stock purchase program
- 11 paid holidays
- 18 PTO days annually
- volunteer time off
- 6 weeks of 100% paid parental leave
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
