Quality Coordinator: Incoming Materials & Documentation

Mindlance, Inc.; Lincoln (NE); Sur place; USD 50 000 - 70 000; Plein temps

Résumé du poste

A national recruiting company is seeking a Quality Coordinator for Incoming Material Inspection in Lincoln, Nebraska. The ideal candidate will have experience in material disposition and laboratory testing, along with the required 2-year Associates degree in a related field. Responsibilities include compiling and reviewing documentation, updating SOPs, and verifying results in laboratory systems. The role demands strong organizational and technical skills, particularly with FDA requirements and LIMS systems.

Qualifications

• Some relevant work experience with material disposition, laboratory testing, LIMS or MRP/ERP systems preferred.
• Experience in the Pharmaceutical industry is a plus.

Responsabilités

• Compile documents for biological and pharmaceutical raw material receipts.
• Perform preliminary review of documentation and specifications.
• Update internal documents to support Quality Operations Team.
• Verify and record results in LIMS and ERP systems.
• Assist with audits and other quality-related activities.

Connaissances

Knowledge of US - FDA requirements

Technical systems skills

Proficient in Microsoft Word

Proficient in Microsoft Excel

Strong organization skills

Detail-oriented processes

Effective communication skills

Formation

2 year Associates degree in Chemistry, Biology or related field

Outils

LIMS (Laboratory Information Management Systems)

ERP (Enterprise Resource Planning) Systems

Microsoft Office

Description du poste

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com.

Job Description

Job Description:
Quality Coordinator (Incoming Material Inspection)
Hours: 7:30 am - 4:00 am; Monday – Friday (1st Shift)

Position Responsibilities:
• Compile documents and supporting documents for biological and pharmaceutical raw material receipts
• Perform preliminary review of documentation and specifications
• Update controlled documents (internal and registered) as needed to support area functions
• Update SOP’s (standard operating procedures) and related documents as needed to support the Quality Operations Team
• Raw material sample handling and archival
• Perform back-up admin duties.
• Verify and record results and/or disposition in the laboratory information management and enterprise resource planning (LIMS/ERP) systems
• Collect/track documentation requested during audits.
• Assist with other activities as requested, including, but not limited to use/support of Quality Systems (both Quality Tracking and Laboratory Information Systems)support of annual product review, risk assessments, change control, supplier management, stability program
• Perform other duties and special projects, as assigned

Education and Experience:
2 year Associates degree in Chemistry, Biology or related field or equivalent post-secondary education or a minimum of 2 years relevant work experience with material disposition, laboratory testing, LIMS or MRP/ ERP computer systems and/or regulatory documentation
Experience with incoming inspection of raw materials within the Pharmaceutical industry preferred.

Technical Skills and Competencies:
Required Candidate Qualifications:
• Some working knowledge of US - FDA, EU and International Registration requirements
• Demonstrated strong technical systems skills
• Proficient in Word and Excel Microsoft applications
• Strong organization skills with proven experience in multi-tasking and prioritizing projects
• Process and detail oriented with the ability to follow complex processes and prepare detailed structured documents
• Demonstrated organizational and administrative skills and the ability to communicate effectively with multiple organizations

Preferred Candidate Qualifications:
• Experience in change management processes, manufacturing/quality operations, laboratory and/or regulatory affairs
• Experience with Training Documentation Systems, Quality Tracking Systems, Laboratory Information Management and Manufacturing Resource Planning Systems (SAP), Microsoft Office applications

Qualifications

Education and Experience:
2 year Associates degree in Chemistry, Biology or related field or equivalent post-secondary education or a minimum of 2 years relevant work experience with material disposition, laboratory testing, LIMS or MRP/ERP computer systems and/or regulatory documentation
Experience with incoming inspection of raw materials within the Pharmaceutical industry preferred.

Preferred Candidate Qualifications:
• Experience in change management processes, manufacturing/quality operations, laboratory and/or regulatory affairs
•Experience with Training Documentation Systems, Quality Tracking Systems, Laboratory Information Management and Manufacturing Resource Planning Systems (SAP), Microsoft Office applications

Additional Information

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

By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply