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Overnight Biotech Quality Control Jobs in Michigan

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Overnight Biotech Quality Control information

What is an overnight biotech quality control?

Overnight Biotech Quality Control jobs involve performing laboratory tests and inspections on biotechnology products during nighttime or overnight shifts. These professionals ensure that products such as pharmaceuticals, biologics, or laboratory samples meet quality and safety standards before they reach the market. Responsibilities often include running assays, documenting results, maintaining equipment, and following strict protocols and Good Manufacturing Practices (GMP). Working overnight helps maintain round-the-clock quality assurance in fast-paced biotech environments. Candidates typically need a background in biology, chemistry, or related fields and attention to detail.

What are the key skills and qualifications needed to thrive as an overnight biotech quality control professional?

To thrive as an Overnight Biotech Quality Control professional, you need a strong background in biology or chemistry, attention to detail, and familiarity with quality assurance practices, often supported by a relevant bachelor's degree. Proficiency in laboratory equipment, data analysis software, and compliance with regulatory standards like GMP or ISO is typically required. Strong problem-solving skills, reliability, and effective communication are important soft skills for this role. These skills are crucial to ensure consistent product quality, regulatory compliance, and effective issue resolution during overnight operations.

What are some common challenges faced by overnight biotech quality control professionals, and how can they be managed?

Overnight Biotech Quality Control professionals often encounter challenges such as working with limited onsite support, maintaining focus during late hours, and responding quickly to unexpected results or equipment issues. Effective communication with day-shift teams and thorough documentation are essential to ensure continuity and avoid errors. Establishing a consistent routine, prioritizing tasks, and utilizing available digital resources can help manage the unique demands of this role and ensure the accuracy and reliability of quality control results.

What is the difference between Overnight Biotech Quality Control vs Microbiologist?

AspectOvernight Biotech Quality ControlMicrobiologist
CredentialsBachelor's in biology, microbiology, or related field; GMP trainingBachelor's or higher in microbiology, biology, or related field; lab certifications
Work EnvironmentLaboratory setting, often overnight shifts, regulated biotech facilitiesLaboratory, research, or clinical settings; may include overnight or day shifts
Industry UsageBiotech, pharmaceutical manufacturing, quality assuranceHealthcare, research institutions, biotech, pharmaceuticals

Overnight Biotech Quality Control specialists focus on testing and ensuring product quality in biotech manufacturing, often working overnight shifts. Microbiologists conduct research, analyze microorganisms, and may work in various settings, including clinical labs. While both roles require microbiology knowledge and lab skills, Quality Control roles emphasize compliance and product safety in biotech environments, whereas Microbiologists may have broader research responsibilities.

What are the most commonly searched types of Biotech Quality Control jobs in Michigan?

The most popular types of Biotech Quality Control jobs in Michigan are:

What are popular job titles related to Overnight Biotech Quality Control jobs in Michigan?

For Overnight Biotech Quality Control jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Overnight Biotech Quality Control jobs in Michigan look for?

The top searched job categories for Overnight Biotech Quality Control jobs in Michigan are:

What cities in Michigan are hiring for Overnight Biotech Quality Control jobs?

Cities in Michigan with the most Overnight Biotech Quality Control job openings:

QC Microbiology Technician (2nd Shift)

Grand River Aseptic Manufacturing

Grand Rapids, MI โ€ข On-site

$18 - $23/hr

Full-time, Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago


Job description

QC Microbiology Technician (2nd Shift)
Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!
Overview of this Position:
The QC Microbiology Technician supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing.
Shift Details: Monday - Thursday, 2:00 pm - 12:00 am
Non-Negotiable Requirements:
  • Bachelor's degree in Microbiology or a related field.
  • 0-2 years related work experience.
  • Must have proficient computer skills in Microsoft Word, Excel, and Outlook.

Preferred Requirements:
  • Associate degree or high school diploma/GED with a minimum of 3 years' related experience.
  • Knowledge of QA principles and procedures in a pharma, biopharma, and/or biotech manufacturing environment.

Responsibilities Include (but are not limited to):
  • Perform sampling of water and pure steam to support manufacturing activities.
  • Perform Environmental Monitoring of isolator and supporting areas.
  • Perform bioburden testing of water an in-process samples to detect microorganisms and to obtain information on types and levels of microbial contamination.
  • Perform Total Organic Carbon, Conductivity, Nitrates, and Endotoxin testing on water.
  • Perform sampling of compressed gas system to support manufacturing activities.
  • Maintain laboratory equipment - cleaning and calibration.
  • Perform daily, weekly, and monthly lab maintenance and stocks supplies.
  • Receive incoming samples for testing.
  • Assist with incoming material testing and inventory.
  • Comply with applicable GMPs.
  • Maintain good practices with regards to processes and/or internal conditions leading to an aseptic environment.
  • Maintain laboratory logbooks and other forms to document proper GLP testing.

Full job description available during formal interview process.
What Sets GRAM Apart from Other Employers:
BENEFITS starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PAID TIME OFF: You choose how to use this time for your vacation, sick, or mental health needs! PTO: Full-time employees accrue up to 104 hours of paid time off per calendar year, with this amount being prorated your first year. WELLNESS TIME OFF (WTO): In addition to PTO, employees earn 1 hour of wellness time off for every 30 hours worked, to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
PAY: Depends on Experience and is discussed during the interview process.
If you meet the required criteria listed above, GRAM welcomes you to apply today!