Weekend Biotech Quality Control Jobs in Chicago, IL

Provide guidance, direction, and coordination of work to the Quality Control staff to ensure continuous production and distribution of products consistent with established standards.  Address quality issues and concerns during production and sample runs; distribute or assign work as needed. Evaluate compliance using relevant information and individual judgment to determine whether events or processes comply with specifications, operating procedures or standards. Duties and responsibilities are accomplished personally or with other Quality Control staff. Indirectly responsible for the work outcomes and productivity of the QC staff. 

Responsibilities; 

• Assist Quality Control Manager in coordinating and executing objectives throughout the company in cooperation with other Lead Quality Inspectors to maximize product quality and operating system efficiency/effectiveness to minimize costs. 

• Direct and coordinate the activities of Quality Inspectors engaged in the evaluation of goods. 

• Perform all the functional duties and responsibilities of the Quality Inspector 

• Plan and establish work schedules, assignments, and production sequences to meet production goals. 

• Read and analyze charts, work orders and other records and reports, in order to determine resource requirements. 

• Review data and documentation for accuracy and correctness and ensure processing is performed within established time expectations. 

• Analyze statistical data to determine adequacy of present standards and establish quality plans. This includes analysis of current inspection methods and sample plans. 

• Assist in the oversight of nonconforming product during the production stage. 

• Ensure all in-process and start-up requirements are met with respect to LRP and usage decision, consult with Quality Control Manager for discrepancies. 

• Prepare necessary quality and safety reports. 

• Consult with management and staff to address work related issues/complaints with support of  Quality Control Manager and Quality Managers. 

• Observe work performed by Quality Inspectors to ensure staff conforms to quality system standards. 

• Participate in investigations regarding customer complaints. 

• Utilize problem solving techniques to reduce internal and external failures. 

• Provide training as needed for the QC department. 

• Executes specific responsibilities as defined within the company quality system. 

• Supports and maintains all policies of the company including but not limited to applicable FDA regulatory and ISO requirements, Health and Safety Requirements and Continuous Improvement initiatives. 

• Coach and mentor employees to ensure they maintain or exceed company and/or department performance expectations.    

• Provide feedback and performance information to Quality Managers to assist in their preparation of Performance Reviews. 

Preferred/Required Education/Skills: 

• Must be able to perform all quality inspector functional job responsibilities Should have good working knowledge of raw materials, production processes, costs and other techniques to maximize the effective manufacture and distribution of product. 

• Must be self-directed and demonstrate skills in planning and organizing  

• Knowledge of inspection tools, use, and maintenance of those tools required. 

• Associates   degree or minimum three (3) years related work experience with one of those years in a lead role preferred. 

• Excellent oral and written communication skills.  

• Ability to apply basic mathematical concepts 

• General knowledge of PC applications such as Microsoft Word, Excel and Database software required.  

• Good understanding of the English language. Able to read, write and speak English. 

Work Environment: 

• Office, production and clean room environment 

• Able to lift up to 35 lbs  

• Able to push and pull items 

• Ability to sit, stand, walk 80% of shift required. 

• Contact with others 75% of daily activity 

•  Ability to travel between office and production departments as well as company buildings required 

All your information will be kept confidential according to EEO guidelines.

Nemera is a world leader in the design, development, and manufacturing of drug delivery devices for the pharmaceutical, biotechnology, & generics industries. With locations worldwide, some of our services and products include eyedroppers, pumps, valves, inhalation devices, airless dispensers, and auto-injectors.
We put patients first when creating drug delivery devices because we know that accurate dosing and ergonomics contribute to patients completing their treatment. Working at Nemera means being part of a team that truly enjoys working together and always goes the extra mile to deliver on its commitments. We're proud of the work we do because it improves patients' lives.
Nemera Buffalo Grove LLC is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other protected class indication. This company is required by federal law to hire only persons who can establish they are eligible to work in the United States.
The Nemera timekeeping system utilizes finger scan. Our biometric policy is available upon request at [email protected]