Analytical Development Scientist
Employer
Proclinical Staffing
Location
Pennsylvania, Bristol, USA
Salary
USD40 - USD45 per hour
Start date
17 Jun 2025
Closing date
1 Jul 2025
categories
Apply now
Job Details
Company
Job Details
Analytical Development Scientist - Contract - Bristol, PA
Ready to assist in bringing life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!
Primary Responsibilities:
You will be instrumental in ensuring data integrity, reviewing laboratory notebooks, and supporting GMP-related documentation processes. This role requires attention to detail and a collaborative approach to meet development goals.
Skills & Requirements:
Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
Expertise in separation-based analytical techniques like HPLC, GC, and CE-SDS.
Experience in reviewing laboratory notebooks and GMP documents.
Familiarity with method development and qualification principles.
Proficiency in document management systems is advantageous.
Knowledge of stability testing and ICH guidelines is preferred.
Understanding of regulatory expectations for early-phase clinical development.
Experience with IND filings and analytical data trending is beneficial.
The Analytical Development Scientist's responsibilities will be:
Review laboratory notebooks for completion, compliance, accuracy, and clarity.
Evaluate the suitability of analytical methods and data for development objectives.
Provide technical support for separation-based assays, including HPLC, GC, and CE-SDS.
Review analytical methods for compliance with internal standards and GMP requirements.
Assess qualification protocols and reports for methods transitioning to quality control.
Support the preparation and review of development reports.
Assist in generating Certificates of Testing for batch release and stability assessments.
Ensure all data and documentation adhere to regulatory and internal compliance standards.
Compensation:
$45 to $50 per hour.
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at ...
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -
Employer
Proclinical Staffing
Location
Pennsylvania, Bristol, USA
Salary
USD40 - USD45 per hour
Start date
17 Jun 2025
Closing date
1 Jul 2025
categories
Apply now
Job Details
Company
Job Details
Analytical Development Scientist - Contract - Bristol, PA
Ready to assist in bringing life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!
Primary Responsibilities:
You will be instrumental in ensuring data integrity, reviewing laboratory notebooks, and supporting GMP-related documentation processes. This role requires attention to detail and a collaborative approach to meet development goals.
Skills & Requirements:
Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
Expertise in separation-based analytical techniques like HPLC, GC, and CE-SDS.
Experience in reviewing laboratory notebooks and GMP documents.
Familiarity with method development and qualification principles.
Proficiency in document management systems is advantageous.
Knowledge of stability testing and ICH guidelines is preferred.
Understanding of regulatory expectations for early-phase clinical development.
Experience with IND filings and analytical data trending is beneficial.
The Analytical Development Scientist's responsibilities will be:
Review laboratory notebooks for completion, compliance, accuracy, and clarity.
Evaluate the suitability of analytical methods and data for development objectives.
Provide technical support for separation-based assays, including HPLC, GC, and CE-SDS.
Review analytical methods for compliance with internal standards and GMP requirements.
Assess qualification protocols and reports for methods transitioning to quality control.
Support the preparation and review of development reports.
Assist in generating Certificates of Testing for batch release and stability assessments.
Ensure all data and documentation adhere to regulatory and internal compliance standards.
Compensation:
$45 to $50 per hour.
If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at ...
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -
Job ID: 481697364
Originally Posted on: 6/18/2025
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