Senior Analytical Chemist - GMP/GLP Leader

Curia Aalborg ApS; New Mexico; Vor Ort; USD 70.000 - 95.000; Vollzeit

Benefits dieser Stelle

Generous benefits

Paid training

Career advancement opportunities

Education reimbursement

401K with match

Learning platform

Zusammenfassung

Curia Aalborg ApS in Albuquerque, NM is seeking a Chemist III to perform advanced analytical testing and provide technical leadership within the Chemistry Department. You will support internal manufacturing and external customer programs, ensuring data integrity and adherence to approved methods and regulatory requirements.

The role involves mentoring junior staff, authoring and reviewing technical documents, and collaborating cross-functionally with Quality, Manufacturing, Validation,

Qualifikationen

• Experience performing analytical testing using standard lab instrumentation.
• Ability to interpret and trend analytical data and summarize findings.
• Mentor junior staff and support method transfers.
• Familiarity with GMP/GLP and regulatory requirements.

Aufgaben

• Serve as SME for analytical testing and instrumentation.
• Perform and review testing of raw materials, in-process samples, finished products, and stability samples.
• Analyze, trend, and summarize data; communicate findings to management and cross-functional teams.
• Create, review, and provide input for protocols, reports, investigations, and change controls.
• Lead or support investigations into deviations, OOS, and OOT events with root cause analysis.
• Provide coaching on documentation practices and training to staff.

Kenntnisse

Analytical testing

Lab instrumentation

Data interpretation

Pipettes and balances

Tools

HPLC

UV/Vis spectrophotometry

TOC analyzers

IR spectroscopy

Jobbeschreibung

Curia Aalborg ApS in Albuquerque, NM is seeking a Chemist III to perform advanced analytical testing and provide technical leadership within the Chemistry Department. You will support internal manufacturing and external customer programs, ensuring data integrity and adherence to approved methods and regulatory requirements.

The role involves mentoring junior staff, authoring and reviewing technical documents, and collaborating cross-functionally with Quality, Manufacturing, Validation,