GMP QC Chemist II: Materials & Release Testing

Experis Austria; South Portland (ME); On-site; USD 45,000 - 48,000; Full time

Job summary

Experis in South Portland, ME is seeking a QC Chemist II to join one of our leading healthcare clients on a 3-month, 100% onsite assignment. This role offers exposure to GMP environments and opportunity to contribute to material release and stability studies.

Responsibilities include performing routine analyses with approved methods, prioritizing workloads to meet timelines, maintaining training status, following GMP documentation, and supporting change controls, OOS/OOT investigations, and

Qualifications

• Bachelor's degree or equivalent required.
• 2-5 years of related work experience with knowledge of GMP
• Proficiency in English required.
• Will perform task in a quality system environment.

Responsibilities

• Performs routine analysis using approved test methods in a timely manner.
• Prioritizes assigned workload to meet the customer’s needs.
• Maintains current status on all training requirements and supports training activities for other laboratory personnel.
• Understands and follows GMP requirements with respect to laboratory operation, testing, results generation, and documentation.
• Carries out change requests/change controls as needed and be able to provide explanations or justifications to the change.
• Recognizes OOS, OOT, and exception events.
• Initiates and conducts investigations under supervision of senior staff.
• Carries out method development, validation, verification, and transfer following protocols.
• Prepares technical protocols and reports under general supervision.
• Maintains a safe working environment per procedures.

Skills

Routine analysis

GMP compliance

English language

Education

Bachelor's Degree

Tools

Analytical testing methods

Job description

Experis in South Portland, ME is seeking a QC Chemist II to join one of our leading healthcare clients on a 3-month, 100% onsite assignment. This role offers exposure to GMP environments and opportunity to contribute to material release and stability studies.

Responsibilities include performing routine analyses with approved methods, prioritizing workloads to meet timelines, maintaining training status, following GMP documentation, and supporting change controls, OOS/OOT investigations, and