QC Scientist II

QC Scientist II – Microbiology

Adecco Healthcare & Life Sciences is hiring for a leading pharmaceutical and life sciences organization known for supporting high-quality drug manufacturing and analytical testing in Greensboro, NC.

Position Details

Location: Greensville, NC
Work Arrangement: 100% Onsite
Pay Rate: Up to $33/hour
Contract: 1-year contract with potential for direct hire
Schedule: Full-time; onsite laboratory environment

Position Overview

The QC Scientist II will perform moderately complex microbiological analyses supporting pharmaceutical manufacturing and quality operations. This position will conduct testing of raw materials, in-process samples, finished products, stability samples, and production intermediates using established, validated, and compendial methods.

The ideal candidate will bring hands-on experience in a pharmaceutical microbiology or regulated laboratory environment , with strong knowledge of microbiological testing, laboratory documentation, instrumentation, and GMP/GLP requirements.

This is a strong opportunity for an experienced microbiology professional looking to expand their experience within a regulated pharmaceutical manufacturing environment.

Key Responsibilities

• Perform microbiological testing of in-process and finished products using established and validated analytical methods.

• Conduct testing including:

  • Bioburden

  • Bacterial Endotoxin Testing (BET)

  • Particulate Matter

  • Sterility

  • Water testing

• Perform qualitative and quantitative microbiological analyses in accordance with laboratory procedures.

• Execute compendial and internally developed analytical methods.

• Recognize and promptly report out-of-specification (OOS), unexpected, or non-routine results .

• Participate in investigations and recommend appropriate solutions to analytical or product-related issues.

• Maintain and troubleshoot laboratory instrumentation as needed.

• Accurately document testing activities, observations, calculations, and results in accordance with established procedures and systems.

• Enter and review analytical results within applicable laboratory systems.

• Prepare and support regulatory documentation associated with internal projects.

• Communicate testing results and project information with internal departments, corporate sites, agencies, and clients as applicable.

• Write and revise SOPs, work instructions, and other laboratory documentation .

• Maintain a clean, organized, and inspection-ready laboratory environment.

• Monitor and maintain inventory of laboratory supplies and testing materials.

• Follow all applicable GMP, GLP, SOP, safety, and regulatory requirements .

• Support continuous improvement initiatives and identify opportunities to improve laboratory processes.

• Work effectively both independently and collaboratively within a cross-functional environment.

Required Qualifications

• Associate degree in Biotechnology, Biology, Chemistry, or another relevant scientific discipline is required.

• Bachelor's degree in Biology, Chemistry, Microbiology, or a related scientific field preferred.

• 3+ years of relevant experience in a pharmaceutical microbiology laboratory or closely related regulated laboratory environment.

• Strong knowledge of microbiological testing principles and laboratory practices.

• Experience with qualitative and quantitative microbiological testing.

• Understanding of microbiological method development and validation.

• Familiarity with pharmaceutical quality and regulatory requirements.

• Ability to read and interpret technical procedures, SOPs, and applicable regulations.

• Strong documentation and technical writing skills.

• Ability to write or contribute to SOPs and method validation documentation .

• Strong mathematical, analytical, problem-solving, and organizational skills.

• Excellent written and verbal communication skills.

• Ability to work independently while contributing effectively within a team environment.

• Highly organized, detail-oriented, adaptable, and self-motivated.

Preferred Experience

Experience with:

• LIMS

• SLIM

• TrackWise

• Documentum

• Laboratory result review/approval

• Qualified checker responsibilities

• Pharmaceutical manufacturing environments

• GMP/GLP-regulated laboratories

• Analytical method validation

Physical & Work Environment

This is a fully onsite laboratory position .

Candidates should be comfortable with:

• Standing and walking for extended periods.

• Periodic stooping, kneeling, crouching, and reaching.

• Lifting, carrying, and moving items weighing approximately 10–35 pounds .

• Performing repetitive hand and finger movements and working at a computer for extended periods.

• Operating laboratory equipment and reading technical materials for prolonged periods.

• Wearing required laboratory PPE, which may include safety glasses, safety shoes, lab coat, nitrile gloves, safety apron, and occasional respiratory protection .

Why Work with Adecco?

• Up to $33/hour

• 1-year contract with potential for direct hire

• Weekly pay

• 401(k) options

• Medical, dental, and vision benefits for eligible employees

• Skills training and professional development resources

• Dedicated Adecco recruiter support

• Opportunity to build experience within a regulated pharmaceutical microbiology environment

If you have 3+ years of pharmaceutical microbiology experience and hands-on expertise with microbiological testing such as bioburden, endotoxin, sterility, particulate matter, or water testing, this is an opportunity worth exploring.

Pay Details: $30.00 to $33.00 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act
• Los Angeles City Fair Chance Ordinance
• Los Angeles County Fair Chance Ordinance for Employers
• San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.