Top 4 Qc associate i Jobs in Birmingham, Al

Reagent QC Associate I
BioGX Inc —Birmingham, AL
- $38,000 - $42,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Computer literacy
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Quality Assurance Associate I
Gabriella White —Pelham, AL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
Quality Assurance Coordinator I-Legacy of Hope-Flexi
UAB Medicine —Birmingham, AL
- PRN
- Nursing
- Bachelor's degree
- Organizational skills
- Paid parental leave
- Health insurance
12d
Center Quality Manager 1
Octapharma —Midfield, AL
- Full-time
- Bachelor of Science
- Writing skills
- Mid-level
- Wellness program
- Health savings account

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Reagent QC Associate I
BioGX Inc —Birmingham, AL
Education and Experience: BS in molecular biology or related field with at least 2 years of hands-on experience in reagents manufacturing.
$38,000 - $42,000 a year
Quick Apply
Quality Assurance Associate I
Gabriella White —Pelham, AL
Forklift certification or willingness to obtain certification within one month of hire. Hearing requirements include the ability to hear clearly during in-…
Quick Apply

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Quality Technician I
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Basic computer skills for Microsoft Outlook, Word, Excel, etc and data entry. Wellbeing tools and resources to support holistic health, including an Employee…
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QC Environmental Monitoring Technician I - 3rd shift - (10:00 PM to 6:30 AM)
American Regent, Inc. —Hilliard, OH
Associate Degree in microbiology, biology or related scientific field preferred. The Environmental Monitoring Team works in concert with and assists the…

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Reagent QC Associate I

BioGX Inc -
Birmingham, AL

Quick Apply

Job Details

Full-time
$38,000 - $42,000 a year

Qualifications

Microsoft Word
Microsoft Excel
Basic math
Word embeddings
English
Molecular biology techniques
Manufacturing facility experience
Bachelor's degree
Pipetting
Research findings presentation
Manufacturing company experience
Molecular biology

Full Job Description

The Reagent QC Associate I is responsible for general laboratory duties focused on Quality Control of standards, controls and panels for commercially available nucleic acid tests and other advanced reagents. The Reagent QC Associate I will work under the direction of the Quality Control Supervisor and is expected to follow standard operating procedures and quality systems documentation.

Essential Duties and Responsibilities (other duties may be assigned):

Coordinates and executes reagent manufacturing Quality Control procedures
Compiles and submits manufacturing QC data and batch records for QA review and approval
Maintains records and clean room environment to comply with good manufacturing practices and standard operating procedures
Assists in inventory management and ordering materials
Assists in the development of reagent manufacturing QC processes and documentation
Assists in maintaining production and laboratory equipment
Assists in the development of physical quality specifications and tests
Assists in testing raw materials for reliability and stability
Assist in transferring processes from development to manufacturing
May assist in process scaleup to transition from pilot lots to full productionscale manufacturing
Complies with ISO 13485 and cGMP standards.
Supports continuous quality improvement

Supervisory Responsibilities: N/A

Qualifications: To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Proven ability to deliver productivity to plan
Must have excellent communication skills (listening, written, verbal, presentation)
Strong technical skills, including a working understanding of molecular biology and biochemistry
Demonstrated analytical, troubleshooting, and problemsolving skills
Proven math skills
Experience with Microsoft Word and Excel
Demonstrated attention to detail
Strong written and verbal communication skills
Proven ability to meet deadlines and work under aggressive timelines
Demonstrated ability to work effectively in a team environment
Accurate and precise manual pipetting and measuring techniques
Experience working with automated dispensing equipment is preferred, but not required

Education and Experience: BS in molecular biology or related field with at least 2 years of hands-on experience in reagents manufacturing. Master’s degree in one of the related fields is preferred.

Language Skills: Must be proficient in writing and communicating in the English language including presentation of data and results. Computer literate with a working knowledge of Microsoft Word and Excel.

Mathematical Skills: Must be consistent with level education.

Reasoning Ability: Good problem solving, judgment and decision-making skill are required. High degree of organizing skill, planning skill, prioritization skill. Multitasking ability.

Certifications, Licenses, Registrations: None required

Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Work entails regularly performing tasks while working at a computer, desk, laboratory bench or automated machine. Work may involve occasional climbing or balance. Work entails occasional lifting and/or moving up to 25 pounds. Work occasionally requires travel between buildings. This is typically completed by foot or by car.

The employee’s sensory modalities (vision, hearing, smell) and physical capabilities (ambulation without mechanical assistance, strength, coordination, dexterity, range of motion) must be sufficient to independently perform duties/functions of the position.

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

This position will involve a combination of office and biotechnology laboratory environments. While performing the duties of this job, the employee may be exposed to hazardous chemicals, blood-borne pathogens, automated equipment, and high levels of noise and vibration. The noise level in the work environment is usually moderate.

About BioGX Inc

BioGX is a global molecular diagnostics solution provider for better health and safety of communities worldwide. Originally developing tests for Water Quality, Food Safety, and Pharma Quality Control, the company has since created one of the largest portfolios of lyophilized syndromic multiplexes for infectious diseases, leading the way for simple yet superior molecular diagnostics.

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qc associate i jobs in birmingham, al

Reagent QC Associate I

Quality Assurance Associate I

Quality Assurance Coordinator I-Legacy of Hope-Flexi

Center Quality Manager 1

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Essential Duties and Responsibilities (other duties may be assigned):

About BioGX Inc

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