Quality Control Analyst III

VIVOS Professional Services, LLC; Portsmouth (NH); On-site; USD 48,216 - 53,726; Full time

Job summary

VIVOS Professional Services, LLC is seeking a Senior Lifesciences Recruitment Specialist for a contract role in the pharmaceutical sector. This position involves applying job skills to various tasks, conducting investigations, and ensuring compliance with quality assurance standards. Ideal candidates will have an Associate’s Degree in a relevant field and experience with laboratory techniques.

Qualifications

• Experience with A280, CE-SDS, icIEF, ELISA, SoloVPE, and qPCR.
• Familiarity with GMP Quality Systems.
• Ability to train team members.

Responsibilities

• Run test samples for In-Process, Lot Release, and Stability studies.
• Write Quality Records and Test Methods.
• Participate in projects like method transfers and new instrument implementation.

Skills

Quality Assurance

Data Integrity

Microbiology

Biochemistry

Education

Associate’s Degree in Microbiology, Biochemistry, or related sciences

Tools

TrackWise

LIMS

Microsoft Office Suite

Job description

Job Title: Senior Lifesciences Recruitment Specialist at VIVOS Professional Services, LLC

Location: Pharmaceutical Client

Contract Duration: 6-12 months

Pay Range: $35.00/hr - $39.00/hr (provided by VIVOS Professional Services, LLC; actual pay based on skills and experience)

Summary

The Senior Lifesciences Recruitment Specialist applies job skills and company policies to complete tasks of increased scope. Works on semi-routine assignments, recognizing deviations from accepted practices and analyzing situations or data of moderate scope.

Responsibilities

• Apply job skills and company policies to various tasks
• Run test samples for In-Process, Lot Release, and Stability studies
• Conduct investigations, transfers, and validations on test samples
• Review assays
• Train team members
• Write Quality Records (Deviations, CAPA, Change Control) and Test Methods
• Participate in projects such as method transfers, new instrument implementation, and method qualifications
• Utilize Microsoft Office Suite (Word, Excel, PowerPoint)
• Operate Laboratory computer systems
• Use GMP Quality Systems like TrackWise and LIMS (if applicable)
• Apply Data Integrity principles in all work aspects, complying with DI policies and procedures

Requirements

Associate’s Degree in Microbiology, Biochemistry, or related sciences. Experience with A280, CE-SDS, icIEF, ELISA, SoloVPE, and qPCR.

Additional Details

• Seniority Level: Associate
• Employment Type: Contract
• Job Function: Quality Assurance
• Industries: Pharmaceutical Manufacturing and Biotechnology Research