Sample Management Associate

Pfizer; Sanford (NC); On-site; USD 41,328 - 53,726; Full time

Benefits offered by this job

Comprehensive Benefits Package

Short-Term Disability (STD)

Long-Term Disability (LTD)

Supplemental and Voluntary Life Insurance

Job summary

A leading pharmaceutical company is seeking a Sample Management Associate to support its Quality Operations department in Sanford, NC. This position involves managing the sample chain of custody, data entry, and adhering to Good Manufacturing Practices (cGMP). Candidates should have relevant experience and strong analytical skills. The role is fully onsite with a pay rate ranging from $30 to $39 per hour and comes with a comprehensive benefits package.

Qualifications

• Minimum of 2-4 years of experience in relevant field or 1-2 years with an Associate's degree.
• Intellectual capability to perform mathematical problems and data analysis.
• Experience with Good Manufacturing Practices (cGMP) is required.

Responsibilities

• Maintain current Good Manufacturing Practices (cGMP) in compliant QC laboratories.
• Perform sample management tasks such as receipt, disposal, and aliquots.
• Ensure sample chain of custody via the global laboratory information management system (gLIMS).
• Conduct daily support activities related to QC laboratories.

Skills

Mathematical problem-solving

Data analysis

Quality control

Knowledge of cGMP

Education

High school diploma or GED

Bioworks certificate/Associate's degree

Job description

Laboratory Information Management System (LIMS)

Microbiology

Data analysis

Sample Management

Current Good Manufacturing Practices (CGMP)

Sample Management Associate

Summary:

The position will support the Pfizer Sanford, NC Quality Operations (QO) department by performing Quality Control (QC) activities associated with clinical and/or commercial products, raw materials, and validation and stability materials. Key responsibilities include management of sample chain of custody, data entry, data transcription, sample receipt, sample disposal, sample aliquot, and stability sample chambering and pulls.

Responsibilities:

• Perform tasks associated with maintaining current Good Manufacturing Practices (cGMP) in compliant QC and Stability laboratories
• May perform sample receipt, disposal, and sample aliquots
• Ensure sample chain of custody via the global laboratory information management system (gLIMS)
• May perform stability sample chambering and stability sample pulls adhering to stability protocols
• Perform data entry and data transcription
• Perform daily support activities related to the QC Microbiology, QC Chemistry, and QC Bioassay laboratories
• Responsible for reporting issues to management and participating in issue resolution (such as reporting quality events and participating in associated laboratory investigations, reporting instrument/equipment issues, assisting with troubleshooting, etc.).

Qualifications:

• High school diploma or GED with a minimum of 2-4 years of experience OR;
• Bioworks certificate/Associate's degree with 1-2 years of experience
• Intellectual capability to perform mathematical problems and perform data analysis
• Experience with Good Manufacturing Practices (cGMP)
• Quality control experience in a laboratory setting

Location/Schedule:

• This is a fully onsite role in Sanford, NC

Please note contractors are engaged to provide services to Pfizer on a temporary basis in connection with a specific assignment. Contractors are hired and employed through Atrium, our third-party payrolling partner.

This job posting is for a temporary role as an employee of Atrium on assignment at Pfizer. The individual selected for this role will be offered the role as an employee of Atrium; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by Atrium upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements.

Pay Rate Range

Min Pay Rate $30

Max Pay Rate $39

Currency USD

Unit hourly

Benefits Information

Comprehensive Benefits Package available based on eligibility

• Short-Term Disability (STD)
• Long-Term Disability (LTD)
• Supplemental and Voluntary Life Insurance