Job Responsibilities:

Perform qualitative and/or quantitative analytical chemistry testing on pharmaceutical raw materials, components, and/or finished products according to policy and procedures at consistently high levels with a focus on quality and efficiency Performs data review activities as required.

▪ Participates in and may lead some QC Team Discussions.

▪ Maintains adequate inventories of reagents, glassware and other supplies.

▪ Maintains current, complete, legible notebooks and laboratory records in compliance with good scientific and regulatory practices.

▪ Writes and executes laboratory investigations for known lab errors and Out of Specification (OOS) results using the current electronic deviation system and/or other QC procedures.

▪ Participates in investigations for PET process areas related to QC processes or data.

▪ Trains QC employees in good analytical techniques, methods and instrumentation based on expertise.

▪ Troubleshoots methods and processes.

▪ Executes laboratory processes in compliance with GMPs, site and corporate policies, standard operating procedures (SOPs) and test methods. Immediately reports deviations that have the potential to compromise product quality.

▪ The role may include shift and weekend work.

▪ Performs testing on a range of samples, including finished products, water, and environmental samples.

▪ May perform sampling activities of various types in the facility (e.g., swabs.).

▪ Dispose of flammable materials in the accumulation container.

▪ Maintains and troubleshoots testing equipment.

▪ Provides and follows up on ideas for continuous improvements in laboratory processes.

▪ Troubleshoots methods and processes.

▪ May serve as an expert in a specific area of laboratory equipment, process, or system.

Typical Accountabilities:

Conduct activities and interactions consistent with Company values and in compliance with the Code of Ethics and supporting Policies and Standards relevant to your role.

▪ Maintains a safe work environment and performs work in accordance with site, Safety, Health, and Environment (SHE) policies and procedures.

▪ Immediately report potential unsafe conditions to management.

▪ Supports internal, external, and regulatory inspections including FDA, EMEA, and third-party inspections

▪ Participates in the investigation and resolution of product quality problems

Education, Qualifications, Skills and Experience- Essentials:

Bachelor degree or a minimum of 3 years of demonstrated relevant experience in Quality Control lab setting.

Schedule:

4x10 schedule 2nd shift 12p-10:30p

Tues-Fri Desirable:

Bachelor of Science degree OR lab experience

▪ working knowledge or experience of GMP environment

Job Type:

Full-time Pay:

$28.22 per hour Expected hours: 40.0 - 50.0 per week

Benefits:

Dental insurance Health insurance Vision insurance

Work Location:

In person