Pharmaceutical Analytical Project Analyst

Groton, MA - USA

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Design and guide analytical strategies to support manufacturing process development.
Lead the planning development execution and data interpretation performed by other scientists in a collaborative matrixed environment.
Oversee and review the development validation and transfer of analytical methods to ensure robust and reliable data generation.
Manage stability studies to assess degradation pathways and establish shelf-life parameters.
Develop impurity control strategies to ensure product quality and regulatory compliance.
Experience with a wide range of analytical testing including dissolution HPLC/UPLC SFC disintegration compendial testing (e.g. excipients / packaging release testing) generic testing (e.g. solvents water ash titrations heavy metals ICP/MS UV) and compound specific methods
Collaborate with cross-functional teams to identify and apply the most effective analytical techniques including the use of computational modeling predictive tools and data visualization platforms.
Evaluate scientific data to draw clear conclusions guide future work and communicate findings through presentations technical reports and other media.
Contribute to regulatory submissions by authoring relevant sections of the quality modules ensuring alignment with global standards and expectations.
Maintain compliance with GLP/GMP standard and safety protocols

Qualifications :

PhD in Chemistry or related field with 3 years of pharmaceutical R&D experience or a B.S./M.S. with 15
Strong oral and written communication skills.
Experience in a regulated laboratory environment (GLP/GMP).
Proven ability to lead scientific projects and mentor team members.
Proficiency in analytical instrumentation and techniques.
Familiarity with regulatory documentation and submission processes.

Additional Information :

Position is full-time Monday-Friday 8:00 am - 5:00 pm.
Candidates currently living within a commutable distance of Groton CT are encouraged to apply
Excellent full-time benefits including comprehensive medical coverage dental and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
#LI-EB1
Authorization to work in the United States indefinitely without restriction or sponsorship

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Remote Work :

Employment Type :

Full-time

Design and guide analytical strategies to support manufacturing process development. Lead the planning development execution and data interpretation performed by other scientists in a collaborative matrixed environment. Oversee and review the development validation and transfer of analytical methods...

Design and guide analytical strategies to support manufacturing process development.
Lead the planning development execution and data interpretation performed by other scientists in a collaborative matrixed environment.
Oversee and review the development validation and transfer of analytical methods to ensure robust and reliable data generation.
Manage stability studies to assess degradation pathways and establish shelf-life parameters.
Develop impurity control strategies to ensure product quality and regulatory compliance.
Experience with a wide range of analytical testing including dissolution HPLC/UPLC SFC disintegration compendial testing (e.g. excipients / packaging release testing) generic testing (e.g. solvents water ash titrations heavy metals ICP/MS UV) and compound specific methods
Collaborate with cross-functional teams to identify and apply the most effective analytical techniques including the use of computational modeling predictive tools and data visualization platforms.
Evaluate scientific data to draw clear conclusions guide future work and communicate findings through presentations technical reports and other media.
Contribute to regulatory submissions by authoring relevant sections of the quality modules ensuring alignment with global standards and expectations.
Maintain compliance with GLP/GMP standard and safety protocols

Qualifications :

PhD in Chemistry or related field with 3 years of pharmaceutical R&D experience or a B.S./M.S. with 15
Strong oral and written communication skills.
Experience in a regulated laboratory environment (GLP/GMP).
Proven ability to lead scientific projects and mentor team members.
Proficiency in analytical instrumentation and techniques.
Familiarity with regulatory documentation and submission processes.

Additional Information :

Position is full-time Monday-Friday 8:00 am - 5:00 pm.
Candidates currently living within a commutable distance of Groton CT are encouraged to apply
Excellent full-time benefits including comprehensive medical coverage dental and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
#LI-EB1
Authorization to work in the United States indefinitely without restriction or sponsorship

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Remote Work :

Employment Type :

Full-time

Key Skills

Project Management Methodology
Project / Program Management
Microsoft Access
PMBOK
Visio
Smartsheet
Project Management
Sharepoint
Microsoft Project
Project Management Lifecycle
Project Coordination
Contracts

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About Company

Eurofins

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and the environment safer, healthier and more sustainable. From the food you eat to the medicines you rely on, Eur ... View more

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