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Research Scientist
3 months ago
Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Our PPD Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides.
As the world leader in serving science, our laboratory professionals bring their dedication to accuracy and quality to deliver groundbreaking innovations.
-Department: Mass Spectrometry, GMP labs
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Location: Middleton, WI
- Lab Based
Notes:Full-time, Benefits, Annual Bonus, 401k Match, PTO, Relocation Assistance Available
- Discover Impactful Work:
Conducts and provides technical mentorship on scientific method development and validation projects and/or other specialty technologies studies OR performs troubleshooting for own and others instruments, methods, procedures, and in writing protocols and reports.
Designs and implements method development/validation and/or extractable/leachable studies independently and interprets and reviews analytical data for self and others OR designs and performs multiple stability and inhalation procedures as well as assists others in performing routine maintenance and troubleshooting on multiple instruments (GC, ICP-MS, LC/MS, GC/MS etc.) and multiple detection techniques (UV, FL, CAD, ELSD, IC etc.), methods and procedures.
Routinely acts as the technical project leader for multiple projects, provide updates, reviews and evaluates data, writes reports and protocols.
- A day in the Life:
- Independently performs analytical method development/optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds or equivalent levels of expertise and experience in mass spectrometry or other related areas such as structural elucidation or extractable leachable testing in a variety of formulations and/or delivery systems. Designs and executes experiments independently for self and others.
- Writes, reviews and critiques study protocols, project status reports, final study reports and other projectrelated technical documents.
- Leads analytical (procedural and instrumental) troubleshooting sessions.
- Assists business development group in technical sales and marketing, and presents posters at technical conferences.
- Leads in preparation and implementation of SOPs and quality systems, as well as developing innovative technology and in evaluating and implementing new capabilities.
- Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP). Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.
- Keys to Success:
- Education and Experience:
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to BS degree plus 7+ years' of experience or MS plus 6+ years' of experience, or PhD plus 4+ years' of experience).
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Knowledge, Skills and Abilities:
- Intermediate knowledge of general chemistry and separation science
- Full understanding of laboratory requirements, SOPs, ICH guidelines, USP requirements and FDA guidance
- Full knowledge of technical operating systems
- Ability to independently optimize analytical methods
- Ability to independently perform root cause analysis for method investigations
- Proven technical writing skills
- Proven problem solving and troubleshooting abilities
- Effective written and oral communication skills as well as presentation skills
- Time management and project management skills
- Ability to mentor others on technical operating systems
- Ability to independently review and understand project proposals/plans
- Ability to work in a collaborative work environment with a team
Physical Requirements / Work Environment
Thermo Fisher Scientific values the health and w