Quality Control Laboratory Analyst (MIcrobiology)
Fort Washington, PA, US
Scientific
Bachelors Degree
Full Time, Temporary
$33.50-$34.60
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Fort Washington, PA, US
$33.50-$34.60
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Quality Control Laboratory Analyst (Microbiology)
Kelly® Science & Clinical is seeking a Quality Control Laboratory Analyst for our client aleader in consumer products located in Fort Washington PA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Day Shift Monday to Friday
Until the end of the year
Must be able to supply own lap top
Pay is $33.50-$34.60 an hour
Job Summary
The Quality Control Laboratory Analyst provides critical testing and technical support within the Microbiology and/or Analytical laboratories. This role is responsible for the collection, processing, and testing of chemical components, raw materials, bulk products, and finished goods to ensure full compliance with specifications, Standard Operating Procedures (SOPs), and pharmacopeia standards (USP). The successful candidate will demonstrate a strong commitment to cGMP, safety, and continuous improvement while acting as a technical resource for the team.
Key Responsibilities
Laboratory Operations & Testing
- Perform testing on raw materials, packaging components, in-process materials, and finished products.
- Conduct cleaning validations and environmental monitoring.
- Manage water sample collection and testing.
- Maintain an accurate inventory of testing supplies and perform temperature monitoring.
- Execute tasks with increasing independence while following USP and other applicable pharmacopeia.
- Documentation & Compliance
- Review, generate, and edit technical documents, including SOPs, laboratory investigations, test protocols, and Annual Product Reviews (APRs).
- Document all activities in strict accordance with cGMP requirements and visual verification processes.
- Identify, report, and seek immediate correction for any workplace deviations.
- Support regulatory inspections and audits by serving as a scribe, runner, or document gatherer.
- Systems & Technical Expertise
- Serve as a “Power User” for laboratory and enterprise systems (LIMS, SAP/ERP, and automated processes).
- Utilize MS Office tools to enhance business effectiveness and data management.
- Maintain a deep understanding of product families, characteristics (viscosity, color), and critical processing parameters for actives and excipients.
- Leadership & Training
- Act as a Subject Matter Expert (SME) and curriculum owner for specific lab functions.
- Partner with the training department to develop curricula and act as a qualified trainer for peers.
- Provide leadership and guidance to less experienced personnel
- Participate in Lean/Continuous Improvement initiatives and Kaizen events.
- Promote a safety-conscious culture by identifying hazards and wearing appropriate PPE.
Qualifications
- Education :Bachelor’s Degree.
- Preferred: Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or a related scientific field.
- Required: Minimum of 1 year of GMP/GLP quality control laboratory experience.
- Experience in a pharmaceutical, OTC, or highly regulated environment is required.
- Technical: Working knowledge of automated systems and electronic batch records.
- Preferred: Basic knowledge or exposure to LIMS.
- Physical Demands
- Ability to perform routine laboratory activities.
- Capable of light to moderate lifting.
- What happens next
Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
Helping you discover what’s next in your career is what we’re all about,
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Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.