Analytical Chemist - HPLC - Job ID: 251802
Medix™, Trenton, NJ, United States
Senior Analytical Scientist (Small Molecule/CDMO)
We are seeking a high-caliber
Analytical Scientist
to join our team during a period of significant growth. This is a critical role supporting QC testing and analytical method validation in a pharmaceutical GMP manufacturing environment.
Compensation:
$40.00 – $48.00 per hour (DOE).
Schedule:
Standard 9am–5pm workday with flexibility; occasional weekday or weekend overtime may be required to meet project milestones.
Reporting:
Direct visibility to the Director.
Key Responsibilities Include:
Comprehensive Testing:
Conducting raw material testing, release/stability testing, and finished product testing (primarily HPLC assay).
Method Validation & Development:
Splitting time between developing and validating methods, including full support for GC analysis and moisture content.
Project Leadership:
Taking ownership of the analytical lifecycle, including reviewing notebook pages and drafting comprehensive validation reports.
Collaborative Innovation:
Working side‑by‑side with the formulation team in the lab to ensure seamless clinical supply manufacturing.
What We’re Looking For We need someone who can hit the ground running. Due to a significant project pipeline over the next two months, we are looking for an adaptable professional who learns quickly.
Must-Have Qualifications:
Experience:
5–8 years of analytical HPLC testing experience in a GMP/QC environment.
Expertise:
Deep proficiency in
HPLC
and
Karl Fischer titration .
Technical Breadth:
Proven experience in assay testing, dissolution, melting point, and moisture testing.
Scientific Mindset:
Ability to validate and troubleshoot HPLC instrumentation. Interest in full ownership of data and reporting.
Background:
Strong focus on
small molecule analysis
(ideally oral solid dosage).
Nice-to-Haves:
CDMO/Generic Manufacturing:
Experience in a Contract Development and Manufacturing Organization is highly preferred.
Inhalation Testing:
Specific experience in inhalation testing is a significant advantage.
Technical Skills:
Experience with GC, FTIR, and method development.
Why Join Us? This role offers the opportunity to specialize in inhalation testing and lead significant validation work for a dedicated client. We value efficiency, thorough reporting, and a proactive attitude. You will be joining a team that is expanding due to success, offering a stable yet exciting environment for a scientist looking to elevate their career.
#J-18808-Ljbffr
Analytical Scientist
to join our team during a period of significant growth. This is a critical role supporting QC testing and analytical method validation in a pharmaceutical GMP manufacturing environment.
Compensation:
$40.00 – $48.00 per hour (DOE).
Schedule:
Standard 9am–5pm workday with flexibility; occasional weekday or weekend overtime may be required to meet project milestones.
Reporting:
Direct visibility to the Director.
Key Responsibilities Include:
Comprehensive Testing:
Conducting raw material testing, release/stability testing, and finished product testing (primarily HPLC assay).
Method Validation & Development:
Splitting time between developing and validating methods, including full support for GC analysis and moisture content.
Project Leadership:
Taking ownership of the analytical lifecycle, including reviewing notebook pages and drafting comprehensive validation reports.
Collaborative Innovation:
Working side‑by‑side with the formulation team in the lab to ensure seamless clinical supply manufacturing.
What We’re Looking For We need someone who can hit the ground running. Due to a significant project pipeline over the next two months, we are looking for an adaptable professional who learns quickly.
Must-Have Qualifications:
Experience:
5–8 years of analytical HPLC testing experience in a GMP/QC environment.
Expertise:
Deep proficiency in
HPLC
and
Karl Fischer titration .
Technical Breadth:
Proven experience in assay testing, dissolution, melting point, and moisture testing.
Scientific Mindset:
Ability to validate and troubleshoot HPLC instrumentation. Interest in full ownership of data and reporting.
Background:
Strong focus on
small molecule analysis
(ideally oral solid dosage).
Nice-to-Haves:
CDMO/Generic Manufacturing:
Experience in a Contract Development and Manufacturing Organization is highly preferred.
Inhalation Testing:
Specific experience in inhalation testing is a significant advantage.
Technical Skills:
Experience with GC, FTIR, and method development.
Why Join Us? This role offers the opportunity to specialize in inhalation testing and lead significant validation work for a dedicated client. We value efficiency, thorough reporting, and a proactive attitude. You will be joining a team that is expanding due to success, offering a stable yet exciting environment for a scientist looking to elevate their career.
#J-18808-Ljbffr