RDMfg Scientist III
RDMfg Scientist III
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Salary Not Disclosed
1 Vacancy
Job Description
Work Schedule
Standard (MonFri)Environmental Conditions
Laboratory Setting Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.Job Description
Do you have a passion for innovative ideas and groundbreaking discoveries With over $1 billion invested annually in R&D at Thermo Fisher Scientific youll help overcome some of the worlds toughest challenges from giving cancer patients hope ensuring safe drinking water and helping law enforcement take on cases through forensics. We empower our employees to put science into meaningful action and give our R&D colleagues the autonomy resources and tools they need to take science a step beyond.
Location/Division Specific Information
Florence SC / Drug Substance
How will you make an impact
Test raw materials samples stability and production intermediates. Test active pharmaceutical ingredients as well. Develop and qualify methods. Ensure products meet quality standards. Collaborate with internal teams. Provide results to teams and clients.
What you will do:
- Perform routine and nonroutine chemical tests and method development/qualification for pharmaceutical raw materials inprocess samples and active pharmaceutical ingredient samples using internally developed and compendial test methods.
- Complete developmental and validated test methods using various analytical techniques such as HPLC GC spectroscopy GC/MS LC/MS and traditional wet chemical testing. Train colleagues on these techniques. Provide thoughtful technical review of data collected by other employees.
- Recognize and report/investigate outofspecification or unexpected results and nonroutine analytical and product problems.
- Craft documentation of the testing/analysis and record the acquired results to sufficiently communicate the works outcomes. Ensure compliance with prescribed lab procedures and systems when reporting the analysis results.
- Assist in writing/reviewing regulatory documents and other communications with outside agencies clients and/or colleagues from other corporate sites. Write and review Analytical Methods validation protocols validation reports and SOPs as needed.
- Problem solving related to the processing of chemical procedures.
- Perform daily instrument calibrations / verifications as required and weekly/monthly inspection of safety equipment.
- Lead projects with minimal supervision; may lead projects including but not limited to managing process development timelines and deliverables coordinating analytical development activities
- Evaluate technical package and successfully lead analytical technology transfer.
How you will get here:
Education
MS degree in chemistry or a related field or equivalent experience; PhD preferred
Experience/Qualifications
- 8 years of working experience in a laboratory preferred (GLP or GMP/cGMP environment preferred) with analytical instrumentation such as HPLC GC spectroscopy GC/MS LC/MS.
- 8 years of working experience with analytical instrumental technologies as well as knowledge of qualitative and quantitative chemical analysis.
- Extensive knowledge of quality and regulatory requirements in the pharmaceutical industry including pharmaceutical GMPs and descriptive organic chemistry. Understanding of medical terminology clinical data and Good Manufacturing Practices (GMP).
Skills & Abilities
- Problem solving skills and logical approach to resolve scientific problems.
- Good interpersonal communication (both oral and written) and presentation skills.
- Ability to read analyze and interpret technical procedures and governmental regulations.
- Ability to write standard operating procedures simple protocols and reports.
- Ability to apply mathematical operations to such tasks as determination of test reliability analysis of variance and correlation techniques.
- Ability to work on multiple projects simultaneously.
- Ability to independently evaluate scientific data and develop actionable plans to troubleshoot and remediate
This position has not been approved for relocation assistance.
We strive to empower our clients to supply a healthier cleaner and safer world. Listen to our colleagues as they share 5 reasons why you should join our company. As a team of 100000 colleagues we are united by values such as integrity intensity innovation and involvement. Working together we accelerate research overcome scientific challenges champion innovation and provide support to patients. Begin your experience at our company where we value diverse experiences and perspectives.
Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.
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Employment Type
Full-Time
