Analytical QC Scientist I - HPLC & GMP

Actalent

Berkeley (MO)

On-site

USD 39,000 - 43,000

Full time

3 days ago

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Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Time Off / PTO

Job summary

Actalent is seeking a Quality Control Scientist I for a fully onsite role in Berkeley, MO. You will perform HPLC/UPLC testing for release, stability, and validations, document data per GMP, and help troubleshoot instrumentation.

The role supports method validation, SOP authoring, and collaboration with QC teams and clients. Ideal candidates have a Bachelor’s in a life sciences field and hands-on experience with chromatography systems, with strong attention to detail and ability to work both

Qualifications

Bachelor's degree in a related scientific field.
Hands-on experience with HPLC/UPLC or other analytical instrumentation.
Strong understanding of analytical laboratory techniques and GMP concepts.
Excellent attention to detail and documentation.
Ability to work independently and collaboratively in a laboratory.

Responsibilities

Perform HPLC/UPLC and other analytical testing for release, stability, and validation studies.
Document and report laboratory data in compliance with GMP requirements.
Identify and communicate OOS/OOT results.
Operate, maintain, and troubleshoot laboratory instrumentation.
Support method validation, qualification, and transfer activities.
Author and revise SOPs and lab documentation.
Maintain safety and compliance in the laboratory.
Collaborate with QC teams, project managers, and clients to prioritize testing.