QC Technician

Business Title: 102221 | QC Technician
Location: Marietta, PA 17547
Job Type: Contract (12 M)

Job Purpose:

• Collect environmental monitoring and utility samples. Collect PEMS data. Perform retain inspections.
• Perform component testing for packaging and process materials such as cartons, syringes, glass vials, tubing, etc.
• Perform routine laboratory tasks such as glassware cleaning and stocking, level one audit, etc.
• Perform tasks associated with ordering laboratory supplies and maintaining laboratory equipment.
• Follow and work in accordance with company policies, SOPs, and cGMP standards to ensure compliance with all applicable regulations.
• Identify atypical events or potential problems and communicate these situations with appropriate personnel.

Job Responsibilities:

• Perform Environmental Monitoring duties related to viable air, viable surfaces, swabs, and non-viable air sample collection as well as performing utility sampling. Perform associated sample reads/testing.
• Generate all paperwork and labels associated with sampling to meet SOP requirements. Collect PEMS data.
• Responsible for assisting senior staff with the harmonization of compendial methods with other vaccine sites. This will include the review of documents, identification of potential gaps, and revision of those documents.
• Handle special projects such as abnormal test results, investigations, and validation studies as needed. Identify data trends and escalate as needed.
• Responsible for maintaining and ordering sufficient reagents and supplies, ordering equipment, and maintaining the equipment in good working conditions in a calibrated and validated status.
• Performing routine laboratory tasks such as safety shower/eyewash checks, autoclaving materials, performing glass-wash and stocking supplies, daily pH meter and balance calibration, etc.
• Ensure labs are in a ‘GMP, safe, analytical-testing readiness’ state.
• Assure that all required documentation including records and logs, is complete and accurate according to the current GMPs. File and archive laboratory records and data by GMPs and SOPs.
• Revise and write change controls, SOPs, and other GMP documents as required.
• When assigned to rotating shift work; work independently and without direct supervision to perform normal operating routines and emergency response procedures.
• Communicate and report the status of operations as well as variances to supervisors. Take appropriate actions and escalate issues immediately.
• Perform all tasks with a safety mindset. Following the EHS guidelines established on site.

Skills & Experience Required:

• High school diploma
• • Associate degree highly preferred
• Knowledge of standard laboratory techniques
• Computer skills required in Excel and Word
• Demonstrate a serious commitment to accuracy and quality while meeting goals or deadlines.

 Preferred qualifications:

• Two years of GMP laboratory testing experience (raw materials, wet chemistry, compendial testing, packaging components).
• Demonstrated familiarity with cGMPs, facility regulatory guidelines, and standard operating procedures.

About the Company:
The Accuro Group

Accuro connects talented financial, professional and technical contributors with the world’s best companies.

Whether you’re interested in rewarding consulting engagements—or advancing your career with a leading organization—Accuro is here to help you navigate this journey.

For more information, visit us online at accurogroup.com

Company Size:
50 to 99 employees

Industry:
Staffing/Employment Agencies

Founded:
2003

Website:
http://accurogroup.com/

Salary : $23 - $28