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QC Analyst III - Tech Transfer

Lenmar Consulting Inc

Portsmouth (NH)

On-site

USD 60,000 - 80,000

Full time

30+ days ago

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Job summary

Lenmar Consulting Inc is seeking a QC Analyst III for their Portsmouth, NH location. The role involves supporting production through quality testing and technical transfer activities, requiring a background in Microbiology or Biochemistry. Ideal candidates will have experience with various testing methods and will be responsible for writing quality records and training team members. This entry-level position offers a full-time employment opportunity in a dynamic environment.

Qualifications

  • Educational background in Microbiology, Biochemistry, or related fields.
  • Experience with quality testing methods like A280, ELISA, and qPCR.
  • Entry-level position requiring problem analysis and technical skills.

Responsibilities

  • Conduct quality testing for in-process, lot release, and stability studies.
  • Write quality records including Deviations and CAPA.
  • Train team members and participate in method transfers.

Skills

A280
CE-SDS
icIEF
ELISA
SoloVPE
qPCR

Education

Microbiology
Biochemistry
Related Science Fields

Tools

Microsoft Office Suite
TrackWise
LIMS

Job description

Join to apply for the QC Analyst III - Tech Transfer role at Lenmar Consulting Inc

1 day ago Be among the first 25 applicants

Join to apply for the QC Analyst III - Tech Transfer role at Lenmar Consulting Inc

Position: QC Analyst III

Location: Fully On-Site

Educational Background: Microbiology, Biochemistry, or Related Science Fields

The Quality Control Technical Transfer Analyst 3 will support the production team by contributing to technical transfer activities. Responsibilities include participating in quality testing for customer in-process, final product testing, and stability studies as needed.

Ideal candidates will have experience with: A280, CE-SDS, icIEF, ELISA, SoloVPE, qPCR.

This role applies job skills and company policies to various tasks, including semi-routine assignments requiring deviation recognition and moderate problem analysis.

Responsibilities
  • Running test samples for In-Process, Lot Release, and Stability studies.
  • Conducting tests for investigations, transfers, and validations.
  • Reviewing assays.
  • Training team members.
  • Writing quality records such as Deviations, CAPA, Change Control, and Test Methods.
  • Participating in projects like method transfers, new instruments, and method qualifications.
  • Utilizing Microsoft Office Suite and laboratory computer systems.
  • Potential use of GMP Quality Systems such as TrackWise and LIMS.
  • Applying Data Integrity principles in all work aspects, in compliance with DI policies and procedures.

Click apply if this position matches your profile. For other industry opportunities, contact lifesci_jobs@vivosps.com.

Additional Details
  • Seniority level: Entry level
  • Employment type: Full-time
  • Job function: Quality Assurance

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