PCI Pharma Services
QC Chemistry Associate II
PCI Pharma Services is seeking a QC Chemistry Associate II to conduct moderate to complex routine analysis of raw materials, proteins, peptides, and small molecules. The role provides moderate supervision and focuses primarily on quality control testing for raw materials, in‑process, and finished formulations.
Job Details The QC Chemistry Associate II works under general supervision and may specialize in a specific area of testing. Typical responsibilities include testing of raw or animal materials, reagents, and intermediates. The position may perform routine analysis and testing according to standard operating procedures in the areas of compliance, applied instrumental analysis, and method development.
Responsibilities
Independently perform routine and moderately complex analysis and testing of raw materials, proteins, peptides, and small molecules, including compendial assays, USP Identification assays, AQL Inspection, UV‑VIS, SoloVPE concentration assays, viscosity, Karl Fischer, and chromatography methods such as HPLC and cIEF.
Review documentation and contribute to accurate report writing.
Support method transfer, qualification, and validation of new methods with minimal supervision.
Maintain and update training documentation.
Provide structured hands‑on training as required.
Lead or contribute to quality event deviation and investigation writing.
Participate in revising and collaborating on documents such as SOPs, protocols, and reports to ensure process improvement and compliance.
Maintain regular and reliable attendance on a full‑time basis and demonstrate professional behavior that reflects positively on PCI Pharma Services.
Embodies PCI Pharma’s cultural values, aligning actions with department goals and company culture.
Requirements
Demonstrated experience in routine and moderately complex analysis of raw materials, proteins, peptides, and small molecules.
Proficiency with compendial assays, USP Identification assays, AQL Inspection, UV‑VIS, SoloVPE concentration assays, viscosity, Karl Fischer, and chromatography methods such as HPLC and cIEF.
Experience in documentation review and report writing with attention to detail and accuracy.
Ability to support method transfer, qualification, and validation of new methods with minimal supervision.
Strong written and verbal communication skills.
Commitment to quality, compliance, and continuous improvement.
Compensation The base hourly range for this position is $29.50 to $33.36, plus annual performance bonus eligibility. Final offer amounts are determined by experience, credentials, geography, and subject‑matter expertise.
Location San Diego, CA
Equal Employment Opportunity (EEO) Statement PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic union status, familial status, gender identity or expression, genetics, disability, military eligibility, veteran status, or any other protected status. We are committed to cultivating an inclusive workplace and holding ourselves accountable to the highest standards of fairness and equal opportunity.
Seniority level Entry level
Employment type Full‑time
Job function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing
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Job Details The QC Chemistry Associate II works under general supervision and may specialize in a specific area of testing. Typical responsibilities include testing of raw or animal materials, reagents, and intermediates. The position may perform routine analysis and testing according to standard operating procedures in the areas of compliance, applied instrumental analysis, and method development.
Responsibilities
Independently perform routine and moderately complex analysis and testing of raw materials, proteins, peptides, and small molecules, including compendial assays, USP Identification assays, AQL Inspection, UV‑VIS, SoloVPE concentration assays, viscosity, Karl Fischer, and chromatography methods such as HPLC and cIEF.
Review documentation and contribute to accurate report writing.
Support method transfer, qualification, and validation of new methods with minimal supervision.
Maintain and update training documentation.
Provide structured hands‑on training as required.
Lead or contribute to quality event deviation and investigation writing.
Participate in revising and collaborating on documents such as SOPs, protocols, and reports to ensure process improvement and compliance.
Maintain regular and reliable attendance on a full‑time basis and demonstrate professional behavior that reflects positively on PCI Pharma Services.
Embodies PCI Pharma’s cultural values, aligning actions with department goals and company culture.
Requirements
Demonstrated experience in routine and moderately complex analysis of raw materials, proteins, peptides, and small molecules.
Proficiency with compendial assays, USP Identification assays, AQL Inspection, UV‑VIS, SoloVPE concentration assays, viscosity, Karl Fischer, and chromatography methods such as HPLC and cIEF.
Experience in documentation review and report writing with attention to detail and accuracy.
Ability to support method transfer, qualification, and validation of new methods with minimal supervision.
Strong written and verbal communication skills.
Commitment to quality, compliance, and continuous improvement.
Compensation The base hourly range for this position is $29.50 to $33.36, plus annual performance bonus eligibility. Final offer amounts are determined by experience, credentials, geography, and subject‑matter expertise.
Location San Diego, CA
Equal Employment Opportunity (EEO) Statement PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic union status, familial status, gender identity or expression, genetics, disability, military eligibility, veteran status, or any other protected status. We are committed to cultivating an inclusive workplace and holding ourselves accountable to the highest standards of fairness and equal opportunity.
Seniority level Entry level
Employment type Full‑time
Job function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing
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