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Overnight Biotech Quality Control Jobs in Michigan

Travel may be required periodically, including overnight stays (contingent on position requirements). * Must be able to lift up to 75 pounds. Join us for an exciting career journey with positive ...

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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:

QA Systems and Document Control Manager

Grand River Aseptic Manufacturing, Inc.

Grand Rapids, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Key responsibilities

  • Manage the lifecycle of controlled documentation, including creation, revision, approval, and maintenance.

  • Oversee key Quality Management System processes such as Non-Conformance Reports (NCRs), Corrective and Preventive Actions (CAPAs), and Change Management.

  • Partner cross-functionally with all departments to support manufacturing and quality objectives.


Job description

Description

 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!
 

Job Description:

The QA Systems and Document Control Manager provides leadership and oversight of Document Control and Quality Systems to ensure compliance with cGMP requirements, quality standards, and regulatory expectations. Manages the lifecycle of controlled documentation, including document creation, revision, approval, and maintenance. Oversees key Quality Management System processes, including Non-Conformance Reports (NCRs), Corrective and Preventive Actions (CAPAs), and Change Management. Serves as a Subject Matter Expert (SME) to drive process effectiveness, continuous improvement, and compliance across the organization. Partners cross-functionally with all departments to support manufacturing and quality objectives. 


Non-Negotiable Requirements:

  •  Bachelor's degree in Life Sciences or a related field and/or 5-10+ years of experience in Quality, Technical Operations, Continuous Improvement, or a related function within the pharmaceutical, biopharmaceutical, biotechnology, or manufacturing industry. 
  •  Strong knowledge of cGMP regulations, FDA requirements, pharmaceutical manufacturing processes, and Quality Assurance principles. 
  •  Experience with process improvement methodologies, including Lean and Six Sigma, and proficiency in Root Cause Analysis (RCA) tools and investigation techniques (e.g., 5 Whys, Fishbone). 
  •  Demonstrated success leading cross-functional teams and driving quality and compliance initiatives across multiple organizational levels 
  •  Experience with electronic Quality Management Systems (eQMS), such as MasterControl or equivalent platforms. 

Responsibilities Include (but are not limited to):

  • Strong knowledge of quality systems, cGMP regulations, and regulatory requirements, with the ability to interpret and apply quality standards across the organization. 
  • Proven leadership and people management skills, including coaching, mentoring, developing teams, and driving accountability. 
  • Excellent written, verbal, and presentation skills, with the ability to effectively communicate and influence stakeholders at all levels. 
  • Strong organizational, analytical, and problem-solving abilities, with demonstrated success managing multiple priorities and meeting deadlines in a fast-paced environment. 
  • Ability to lead cross-functional initiatives, build collaborative relationships, and drive alignment toward quality and business objectives. 
  • Results-oriented professional with a continuous improvement mindset and experience implementing process improvements to enhance compliance, efficiency, and effectiveness. 
  • Demonstrates high levels of integrity, professionalism, sound judgment, urgency, and customer focus. 

Full job description available during formal interview process.

What Sets GRAM Apart from Other Employers:

MEDICAL BENEFITS starting day 1: Blue Cross Blue Shield medical and dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying for 75% 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!

PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!

WELLNESS TIME OFF: Employees earn 1 hour of 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!