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

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

Job summary

A leading company in pharmaceutical manufacturing is seeking a Quality Control Technician II to provide crucial support within their Quality Control department at the Swiftwater, PA site. This 12-month contract role involves maintaining strict compliance with quality standards and regulatory requirements while offering the opportunity to work in a dynamic and innovative environment.

Qualifications

• 2+ years’ experience in a cGMP laboratory setting.
• Understanding of regulatory requirements and compliance.

Responsibilities

• Provide instrumentation support for Quality Control Laboratory.
• Assist in change controls and author cGMP documentation.
• Support QC laboratory inspection readiness.

Skills

cGMP's

Regulatory requirements

Data integrity concepts

Cross-functional collaboration

Analytical instrumentation

Education

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

Job description

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

Join to apply for the USA - Quality Control Technician II (Manufacturing/Quality) 1st Shift (contract) role at Sanofi

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

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Join to apply for the USA - Quality Control Technician II (Manufacturing/Quality) 1st Shift (contract) role at Sanofi

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

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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