Analytical Chemistry Specialist.

détails du poste

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détails du poste

Randstad is looking, for an Analytical Chemistry Specialist with experience in peptides and drug substance analytics. If you have a strong technical background in this area and want to work for a leading company in the sector, this opportunity is for you.

 

Responsibilities:

 

  • Conduct analysis and characterization of peptides using various analytical techniques.
  • Ensure that all critical analytical parameters for peptides — such as purity, identity, and content — are properly defined and validated.
  • Confirm the use of appropriate, validated methods for batch verification, including HPLC, LC-MS, and NMR.
  • Oversee stability studies according to ICH guidelines to ensure the peptide maintains integrity in its solid form.
  • Set and maintain acceptance criteria for release testing, aligned with regulatory and internal quality standards.
  • Review and approve the CMO’s manufacturing processes, including:

          Drying and solidification techniques (e.g., lyophilization).

          Storage conditions (temperature, humidity, packaging).

          Use of excipients, if applicable.

  • Define Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs) relevant to solid-state peptides — such as residual solvents, moisture content, and solid form stability.
  • Ensure appropriate controls are in place to detect impurities or degradation, such as aggregation, oxidation, deamidation, and racemization.
  • Review and approve the analytical methods used by the CMO to ensure they meet regulatory and scientific standards.
  • Oversee identity testing (to confirm correct amino acid sequence) and impurity profiling.
  • Ensure that all testing and controls at the CMO are performed under GMP-compliant conditions.
  • Participate in batch record review and deviation management, including the evaluation of borderline or out-of-specification results.
  • Monitor ongoing trend analysis to identify potential quality or process issues early.

 

 

Requirements:

  • 5 to 10 years of experience in analytical chemistry applied to peptides.
  • Proficiency in analytical techniques for peptides, including; HPLC, LC-MS, CE, CD Spectrometry, NMR Spectroscopy.
  • Experience in method development and validation.
  • Familiarity with GMP regulations and pharmaceutical compliance standards.
  • Advanced English proficiency (mandatory), German knowledge is a plus.
  • Ability to work in a team and in a highly regulated environment.

 

Benefits:

  • Opportunity to work in a leading pharmaceutical company.
  • Professional development in an international environment.
  • Competitive salary and attractive benefits package.

 

If you meet the requirements and are interested in this position, please send your updated CV.

 

We look forward to meeting you soon!

Randstad is looking, for an Analytical Chemistry Specialist with experience in peptides and drug substance analytics. If you have a strong technical background in this area and want to work for a leading company in the sector, this opportunity is for you.

 

Responsibilities:

 

  • Conduct analysis and characterization of peptides using various analytical techniques.
  • Ensure that all critical analytical parameters for peptides — such as purity, identity, and content — are properly defined and validated.
  • Confirm the use of appropriate, validated methods for batch verification, including HPLC, LC-MS, and NMR.
  • Oversee stability studies according to ICH guidelines to ensure the peptide maintains integrity in its solid form.
  • Set and maintain acceptance criteria for release testing, aligned with regulatory and internal quality standards.
  • Review and approve the CMO’s manufacturing processes, including:

          Drying and solidification techniques (e.g., lyophilization).

          Storage conditions (temperature, humidity, packaging).

          Use of excipients, if applicable.

  • Define Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs) relevant to solid-state peptides — such as residual solvents, moisture content, and solid form stability.
  • Ensure appropriate controls are in place to detect impurities or degradation, such as aggregation, oxidation, deamidation, and racemization.
  • Review and approve the analytical methods used by the CMO to ensure they meet regulatory and scientific standards.
  • Oversee identity testing (to confirm correct amino acid sequence) and impurity profiling.
  • Ensure that all testing and controls at the CMO are performed under GMP-compliant conditions.
  • Participate in batch record review and deviation management, including the evaluation of borderline or out-of-specification results.
  • Monitor ongoing trend analysis to identify potential quality or process issues early.

 

 

Requirements:

  • 5 to 10 years of experience in analytical chemistry applied to peptides.
  • Proficiency in analytical techniques for peptides, including; HPLC, LC-MS, CE, CD Spectrometry, NMR Spectroscopy.
  • Experience in method development and validation.
  • Familiarity with GMP regulations and pharmaceutical compliance standards.
  • Advanced English proficiency (mandatory), German knowledge is a plus.
  • Ability to work in a team and in a highly regulated environment.

 

Benefits:

  • Opportunity to work in a leading pharmaceutical company.
  • Professional development in an international environment.
  • Competitive salary and attractive benefits package.

 

If you meet the requirements and are interested in this position, please send your updated CV.

 

We look forward to meeting you soon!

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