Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)
Job Description
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
Join our team as an MSAT TT Scientist II at Thermo Fisher Scientific where youll contribute to pharmaceutical research and development. Youll perform complex analytical testing develop and validate methods and ensure product quality while collaborating with cross-functional teams. This role offers the opportunity to work with advanced technology and contribute to life-changing healthcare solutions. Youll conduct sophisticated chemical and physical testing lead technology transfer activities and support manufacturing operations. Working closely with internal teams and clients youll help advance pharmaceutical development while maintaining the highest standards of quality and compliance.
Discover Impactful Work!
- Technically supports day-to-day operations in the Formulation Filling and/or Freeze Drying areas of the Steriles plant.
- Works on technical/scientific process/product/project activities to implement strategies and technical solutions.
- Assists in the creation of processes single use systems and equipment designs for clinical scale up and/or registration batches including technology transfer of projects from clients.
- Makes decisions that involve direct application of technical knowledge.
A Day in the Life.
- Complete studies tech transfer commercial scale-up and support process validation.
- Represent the organization on internal technical discussions.
- Actively participate in problem solving and project results for formulations equipment and processes.
- Write/revise work orders for existing processes FORMs reports memos and protocols.
- Lead projects with a moderate level of supervision implement change control actions review and plans technical aspects of the project to meet timeline and project goals.
- Support manufacturing operations change controls investigations as subject matter expert (SME).
- Collects data for statistical analysis. Can support interpretation and summary of data.
REQUIREMENTS:
Advanced Degree no prior experience required or Bachelors Degree plus 2 years of experience in pharmaceutical or related industry preferably in GMP/GLP environment
Preferred Fields of Study: Chemistry Biochemistry Biology Pharmaceutical Sciences or related physical science field
Extensive hands-on experience with analytical instrumentation including HPLC GC LC/MS spectroscopy and dissolution testing
Strong knowledge of pharmaceutical GMPs regulatory requirements and quality systems
Proven expertise in method development validation and transfer of analytical methods
Experience with data analysis interpretation and technical writing of protocols and reports
Proficiency in Microsoft Office Suite and analytical software systems
Strong analytical and problem-solving capabilities
Demonstrated project management abilities and capacity to manage multiple projects
Effective written and verbal communication skills for both technical and non-technical audiences
Ability to work both independently and collaboratively
Physical requirements include standing for extended periods lifting up to 35 pounds and working with laboratory equipment
Must be able to follow safety protocols and wear appropriate PPE as required
Demonstrated alignment with company values of Integrity Intensity Innovation and Involvement
Required Experience:
IC
Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job DescriptionAs part of the Thermo Fisher Scientific...
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)
Job Description
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
Join our team as an MSAT TT Scientist II at Thermo Fisher Scientific where youll contribute to pharmaceutical research and development. Youll perform complex analytical testing develop and validate methods and ensure product quality while collaborating with cross-functional teams. This role offers the opportunity to work with advanced technology and contribute to life-changing healthcare solutions. Youll conduct sophisticated chemical and physical testing lead technology transfer activities and support manufacturing operations. Working closely with internal teams and clients youll help advance pharmaceutical development while maintaining the highest standards of quality and compliance.
Discover Impactful Work!
- Technically supports day-to-day operations in the Formulation Filling and/or Freeze Drying areas of the Steriles plant.
- Works on technical/scientific process/product/project activities to implement strategies and technical solutions.
- Assists in the creation of processes single use systems and equipment designs for clinical scale up and/or registration batches including technology transfer of projects from clients.
- Makes decisions that involve direct application of technical knowledge.
A Day in the Life.
- Complete studies tech transfer commercial scale-up and support process validation.
- Represent the organization on internal technical discussions.
- Actively participate in problem solving and project results for formulations equipment and processes.
- Write/revise work orders for existing processes FORMs reports memos and protocols.
- Lead projects with a moderate level of supervision implement change control actions review and plans technical aspects of the project to meet timeline and project goals.
- Support manufacturing operations change controls investigations as subject matter expert (SME).
- Collects data for statistical analysis. Can support interpretation and summary of data.
REQUIREMENTS:
Advanced Degree no prior experience required or Bachelors Degree plus 2 years of experience in pharmaceutical or related industry preferably in GMP/GLP environment
Preferred Fields of Study: Chemistry Biochemistry Biology Pharmaceutical Sciences or related physical science field
Extensive hands-on experience with analytical instrumentation including HPLC GC LC/MS spectroscopy and dissolution testing
Strong knowledge of pharmaceutical GMPs regulatory requirements and quality systems
Proven expertise in method development validation and transfer of analytical methods
Experience with data analysis interpretation and technical writing of protocols and reports
Proficiency in Microsoft Office Suite and analytical software systems
Strong analytical and problem-solving capabilities
Demonstrated project management abilities and capacity to manage multiple projects
Effective written and verbal communication skills for both technical and non-technical audiences
Ability to work both independently and collaboratively
Physical requirements include standing for extended periods lifting up to 35 pounds and working with laboratory equipment
Must be able to follow safety protocols and wear appropriate PPE as required
Demonstrated alignment with company values of Integrity Intensity Innovation and Involvement
Required Experience:
IC
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