QC Analyst, Micro - 2nd Shift

Insight Global; Malvern (Chester County); On-site; USD 65,000 - 90,000; Full time

Job summary

Insight Global is seeking a QC Microbiology Analyst to support Quality Control in a GMP-regulated manufacturing environment. The role involves routine microbiological testing, documenting results, and ensuring product quality and compliance.

Candidates with prior QC microbiology experience from pharma, biotech, or related regulated industries are encouraged to apply. You will perform bioburden and endotoxin testing, plate reading, and help with environmental monitoring while maintaining

Qualifications

• Bachelor's degree in Microbiology, Biology, Chemistry, Biochemistry, or related discipline.
• Experience in a GMP-regulated environment.
• Hands-on microbiology capabilities in testing.
• Solid documentation practices and data integrity mindset.
• Ability to work second shift and meet tight timelines.

Responsibilities

• Perform routine microbiological testing including bioburden and endotoxin testing and plate reading.
• Document results accurately and ensure data integrity.
• Maintain equipment, media preparation, and sample management.
• Collaborate with Quality, Manufacturing, and Laboratory teams on status and priorities.

Skills

Bioburden Testing

Endotoxin Testing

Plate Reading

Laboratory documentation practices

Attention to detail

Independent on second shift

Communication and teamwork

QC laboratory experience

Regulated industry experience

Environmental monitoring programs

Laboratory systems (LIMS, Empower, MES

TrackWise

Education

Bachelor's Degree in Microbiology, Biology, Chemistry, Biochemistry, or related scientific discipline

Job description

Job Description

We are seeking a QC Microbiology Analyst to support Quality Control laboratory operations within a GMP-regulated manufacturing environment. This individual will be responsible for performing routine microbiological testing, documenting results, and supporting laboratory activities that ensure product quality and compliance. This role is ideal for candidates with prior QC microbiology experience who enjoy working in a laboratory environment and want to gain experience within a highly regulated pharmaceutical manufacturing setting. Candidates from pharmaceutical, biotechnology, food, environmental, consumer products, or other regulated industries are encouraged to apply.

Key Responsibilities

Microbiology Testing

Perform routine microbiological testing including bioburden testing, endotoxin testing, and plate reading activities.

Execute testing in accordance with approved methods, SOPs, and GMP requirements.

Analyze samples and document results accurately and efficiently.

Review test data for completeness and compliance.

Support environmental monitoring and other microbiological testing activities as needed.

Laboratory Operations

Maintain laboratory equipment, materials, and supplies.

Support media preparation, reagent preparation, and sample management activities.

Assist with laboratory organization and housekeeping activities.

Ensure testing areas remain inspection ready and compliant with quality standards.

Follow all laboratory safety and compliance requirements.

Quality & Documentation

Record and review laboratory data within electronic systems and laboratory documentation.

Follow GMP, quality, and data integrity requirements.

Support investigations, deviations, CAPAs, and corrective actions as needed.

Assist with SOP revisions, training activities, and continuous improvement initiatives.

Maintain accurate and timely documentation of all testing activities.

Cross-Functional Support

Partner with Quality, Manufacturing, and Laboratory teams to communicate testing status and priorities.

Support operational goals and changing business needs.

Participate in team meetings and improvement initiatives.

Work independently while effectively managing workload and timelines.

Skills and Requirements

Bachelor's Degree in Microbiology, Biology, Chemistry, Biochemistry, or related scientific discipline.

Experience working in a GMP-regulated environment.

Hands-on experience with:

• Bioburden Testing
• Endotoxin Testing
• Plate Reading
• Familiarity with laboratory documentation practices
• Strong attention to detail and organizational skills
• Ability to work independently on second shift
• Strong communication and teamwork skills
• Previous Quality Control (QC) laboratory experience
• Pharmaceutical, biotechnology, medical device, food, consumer product, or environmental laboratory experience
• Experience with environmental monitoring programs
• Familiarity with laboratory systems such as LIMS, Empower, MES, LES, or TrackWise
• Experience supporting laboratory investigations, deviations, or CAPAs

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [e-mail].