USA - Quality Control Technician II (Manufacturing/Quality) 1st Shift (contract)

卡湯晩; Swiftwater (Monroe County); On-site; USD 10,000 - 60,000; Full time

Job summary

Sanofi's FLEXT Direct program is hiring a Quality Control Technician for a 12-month onsite contract in Swiftwater, PA. The role involves supporting QC laboratory instrumentation, ensuring compliance with cGMP standards, and contributing to maintaining high-quality manufacturing processes. Ideal candidates will have a degree in Life Sciences or Engineering and relevant laboratory experience.

Qualifications

• 2+ years’ experience in a cGMP laboratory setting.
• Vaccinations as required.

Responsibilities

• Provide instrumentation support impacting the Quality Control Laboratory.
• Assist in completing change controls, deviations, CAPA's.
• Author cGMP documentation such as protocols and reports.
• Aid in implementing new technologies for QC testing efficiency.

Skills

Working knowledge of cGMP's

Ability to work cross-functionally

Lead projects related to analytical instrumentation

Aptitude working within computerized systems

Understanding of analytical instrumentation concepts

Education

Bachelor's or Master's degree in Life Sciences or Engineering

Job description

Sanofi's contingent workforce program, FLEXT Direct, is seeking a Quality Control Technician for a ONSITE 12- month contract in Swiftwater, PA.

Job Summary

This position at the Swiftwater, PA location involves providing crucial support for the lifecycle management of instrumentation within the Quality Control department. The role requires strict adherence to Sanofi procedures, Health Authority Regulations, and cGMP's to ensure quality standards are met.

Responsibilities

• Provide instrumentation support impacting the Quality Control Laboratory including qualification, calibration, and preventive maintenance
• Assist in completing change controls, deviations, CAPA's to meet timelines
• Author cGMP documentation such as protocols, reports, procedures, and user requirement specifications
• Aid in implementing new technologies to enhance QC testing efficiency and capabilities
• Support QC laboratory inspection readiness
• Develop an understanding of best practices for optimal equipment operation and compliance with regulatory requirements
• Follow cGMPs and adhere strictly to Sanofi policies and procedures
• Complete required training as assigned
  
  
  

Skills

• Working knowledge of cGMP's, Regulatory requirements, and data integrity concepts
• Ability to work cross-functionally with other departments and stakeholders
• Lead projects related to analytical instrumentation
• Aptitude working within computerized systems
• Understanding of analytical instrumentation concepts and technologies
  
  
  

Qualifications

• Bachelor's or Master's degree in Life Sciences or Engineering is required
• 2+ years’ experience in a cGMP laboratory setting
• Vaccinations as required
  
  
  

Exciting Job Opportunity

This role offers the opportunity to work in a dynamic environment where you can contribute to maintaining high-quality standards in pharmaceutical manufacturing. You will be part of a team that values innovation, compliance, and continuous improvement while ensuring patient safety. Join us in making a difference in healthcare through your expertise and dedication.

Pay Rate Range

Min Pay Rate Max Pay Rate Currency Unit 25 34 USD hourly