QC Analyst I/II-Microbiology (2nd Shift)

Planet Pharma; Memphis (TN); On-site; USD 28,929 - 33,062; Full time

Job summary

A leading pharmaceutical company in Memphis is seeking a Quality Control Analyst for the QC Microbiology Department. This role involves essential duties such as conducting environmental monitoring, product release testing, and handling raw materials. Candidates should possess a Bachelor's degree in a scientific discipline and relevant laboratory experience. Strong communication skills and attention to detail are critical for success in a fast-paced environment. The position offers competitive pay and a contract employment type.

Qualifications

• 0‑2 years relevant laboratory experience or experience in a cGMP and/or FDA regulated industry.
• Ability to work in Clean Room environment with full gowning requirements.
• Demonstrated knowledge in Microbiology and aseptic techniques.

Responsibilities

• Perform environmental monitoring, including air viable particulate, non‑viable particulate and surface sampling.
• Receives raw materials and maintains laboratory supplies inventory.
• Adhere to SOP and GCP for data integrity.

Skills

Attention to detail

Organizational skills

Communication skills

Problem-solving

Teamwork

Education

Bachelor's degree in biology or a relevant scientific discipline

Tools

Laser particle counters

Viable air samplers

Microscope

Endosafe® Instrumentation

PCR

BacT/ALERT systems

MODA

LIMS

Job description

QC Analyst I/II-Microbiology (2nd Shift)

Leveling:

• QC I set Pay: $21/hr
• QC II set Pay: $24/hr (Must have at least 2 years of relevant experience)

Position Summary (QC I)

The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product‑release testing, and raw material testing. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast‑paced, highly technical environment with minimal supervision are essential for success.

Essential Duties and Responsibilities (QC I)

• Performs environmental monitoring, including air viable particulate, non‑viable particulate and surface sampling and personnel monitoring
• Receives raw materials and supplies for the QC laboratory and maintains laboratory supplies, media and reagents inventory
• Adheres to SOP and GCP to ensure data integrity and traceability
• Participates in maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.)
• Assists with routine laboratory upkeep and organization
• Utilizes GMP systems such as MODA and other laboratory computer systems
• Reviews test results of other QC analysts for accuracy and precision and maintains an efficient workflow of all required testing documentation ensuring timely submission relative to product release dates
• Performs all other related duties as assigned

Qualifications (QC I)

• Bachelor's degree in biology or a relevant scientific discipline required
• Minimum 0‑2 years relevant laboratory experience or experience in a cGMP and/or FDA regulated industry or a combination of education and related work experience required
• May consider less education and professional experience upon successful completion of the company's internship program
• Ability to work in Clean Room environment with full gowning requirements
• Ability to work independently or as a team member
• Detail‑oriented with strong written and verbal communication skills
• Demonstrated knowledge in Microbiology and aseptic techniques
• Ability to problem‑solve and troubleshoot as necessary
• Familiarity with laser particle counters, viable air samplers, microscope, Endosafe® Instrumentation, PCR, BacT/ALERT systems

Position Summary (QC II)

The Quality Control Analyst II for the QC Microbiology Department will be responsible for performing routine environmental monitoring, product testing, and raw material testing. The position requires the utmost attention to detail, very strong organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast‑paced, highly technical environment with minimal supervision are essential for success.

Essential Duties and Responsibilities (QC II)

• Performs sterility testing and endotoxin testing of raw materials, in‑process samples and finished products
• Performs growth promotion of microbial media
• Performs environmental monitoring, including air viable particulate, non‑viable particulate and surface sampling and personnel monitoring
• Prepares environmental monitoring excursion reports and conducts minor laboratory investigations
• Receives raw materials and supplies for the QC laboratory and maintains laboratory supplies, media and reagents inventory
• Adheres to SOP and GCP to ensure data integrity and traceability
• Assists the QC Supervisor/Leads with managing proper overall operation of department (physical inventories, logs, documentation, filing, etc.)
• Maintains familiarity with QC‑relevant current Good Manufacturing Practices (cGMP) guidance (CFR, USP, EP, ICH, etc.)
• Responsible for assisting with routine laboratory upkeep and organization
• Reviews test results of other QC analysts for accuracy and precision and maintains an efficient workflow of all required testing documentation ensuring timely submission relative to product release dates
• Performs other related duties as assigned

Qualifications (QC II)

• Bachelor's or higher degree in the biological sciences or related field required
• Minimum of 1‑2 years relevant laboratory experience or experience in a cGMP/FDA regulated industry, or a combination of years of educated and relevant laboratory experience required
• Demonstrated knowledge in Microbiology and aseptic techniques required
• Ability to work independently or as a team member
• Ability to work in Clean Room environment with full gowning requirements
• Ability to problem‑solve and troubleshoot as necessary
• Detail‑oriented with strong written and verbal communication skills
• Familiarity with laser particle counters, viable air samplers, microscope, Endosafe® Instrumentation, PCR, BacT/ALERT systems preferred
• Familiarity with laboratory data systems such as MODA, LIMS, etc preferred

Seniority Level

Associate

Employment Type

Contract

Job Function

Science

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing