Quality Control Microbiology Data Review
$36 per hourRandstad
Job Description
Job Description
The Individual will support cGMP QC activities for raw materials, drug substances, and finished products at the company's manufacturing facility. This role includes performing data review of Quality Control test records, EM results, Logbooks, and Lab Notebooks.Here’s What You’ll Need (Basic Qualifications) Education: DegreeExperience: STEM degree; experience in a cGMP laboratory setting, with hands-on experience in microbiology techniques is preferred, but not required.Here’s What You’ll Bring to the Table (Preferred Qualifications)
- Experience with microbiology test methods (growth promotion, bioburden, culture purity, endotoxin).
- Experience with environmental monitoring
- Experience in technical writing
- Familiarity with electronic databases (e.g. LIMS, MODA, SAP).
- Understanding of relevant and current FDA, EU, ICH guidelines and regulations.
- Experience with laboratory equipment calibration and maintenance.
- Experience with microbiology test methods (growth promotion, bioburden, culture purity, endotoxin).
- Experience with environmental monitoring
- Experience in technical writing
- Familiarity with electronic databases (e.g. LIMS, MODA, SAP).
- Understanding of relevant and current FDA, EU, ICH guidelines and regulations.
- Experience with laboratory equipment calibration and maintenance.
shift: Second
work hours: 2 PM - 10 PM
education: Associate
Responsibilities
Here's What You’ll Do
- Review executed QC test records for product release (including Environmental Monitoring Data).
- Review Logbooks and Laboratory Notebooks.
- Supports authoring and revision of laboratory procedures, test record forms and reports.
- Participate in quality systems records such as deviations, change controls, CAPAs, and non-conformance investigations.
- Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.
- Ensure compliance with cGMP documentation and regulatory guidelines.
- Establish and maintain a safe laboratory working environment.
- Provide support during internal and vendor audits and collaborate on continuous improvement initiatives.
- Quality Control
- Quality Assurance
- Inspection
- Years of experience: 2 years
- Experience level: Experienced
Qualifications
Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on ziprecruiter.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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