Planet Pharma
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
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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
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