Quality Lab Senior Supervisor – Night Shift

5 years years

$88,000 – $121,000 annually

North Carolina

10 Sept. 8, 2025

Job Description

Job Type: Full Time Education: Bachelor’s Degree in Life Sciences (e.g., Biology, Microbiology, or related). Master’s Degree preferred (with equivalent industry experience). Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🧪 Position Title:

Quality Lab Senior Supervisor – Night Shift
Req #: JR-183634
Location: Marion, North Carolina, United States
Facility Address: 65 Pitts Station Rd, Marion, NC 28752
Shift: 12-Hour Night Shift (7:00 PM – 7:00 AM)
Team Size: 10–12 direct reports (Lab Supervisor(s) and Quality Lab Technicians)

🌟 Position Summary

As a Quality Lab Senior Supervisor, you will lead the operations and personnel of the QC Particulate Matter (PM) Laboratory, ensuring compliance with USP <1790> and USP <788>. You’ll also provide adjacent leadership for QC Microbiology operations occurring during the night shift.

This role requires a balance of people leadership, technical expertise, documentation compliance, and the ability to drive process improvements while maintaining product safety and quality.

📋 Key Responsibilities

🧑‍🔬 Lab Operations & Leadership

Supervise all night shift operations in the QC PM Lab.
Ensure testing and documentation are compliant with USP <1790> and <788>.
Oversee PM Characterization and Identification procedures.
Assign tasks, set priorities, and ensure performance of team members.
Cross-train and support other areas of the QC Microbiology Laboratory.
Perform troubleshooting and guide team through technical or equipment issues.

🧾 Documentation & Compliance

Lead non-conformance investigations in TrackWise 8.
Conduct Phase 1 Laboratory investigations for PM and assist other QC areas.
Review lab data and documentation for completeness and accuracy.
Ensure timely delivery of results to document control for product release.
Ensure strict adherence to Good Documentation Practices (GDP) and GMP.

👥 People Management & Development

Conduct training, performance check-ins (ACE), and team communications.
Coach, mentor, and develop team members to meet performance expectations.
Foster an environment of trust, feedback, and open communication.

🛡️ Safety & Quality

Enforce and monitor laboratory safety protocols.
Promote a culture where patient safety and quality always come first.

🎓 Qualifications

📚 Education:

Bachelor’s Degree in Life Sciences (e.g., Biology, Microbiology, or related).
Master’s Degree preferred (with equivalent industry experience).

🧪 Experience:

Minimum 5 years’ experience in a pharmaceutical, biotech, or medical device setting.
Hands-on knowledge of aseptic technique and USP testing methodology.
Experience using TrackWise, LIMS, or other quality systems.

🧠 Skills & Competencies:

Strong technical knowledge of FDA, cGMP, GLP, and USP requirements.
Proficient in Microsoft Office Suite (Word, Excel).
Able to manage multiple priorities, work independently, and meet deadlines.
Excellent leadership, communication, and interpersonal skills.
Capable of building a team culture focused on trust, development, and results.

🧯 Working Conditions

Work performed in laboratory and manufacturing environments.
Use of PPE required (lab coats, safety glasses, gloves, earplugs, hairnets, shoe covers).
Must be able to respond to on-shift escalations and handle investigations.
Standing for extended periods and working in a controlled cleanroom environment may be required.
Overtime may be necessary depending on operational needs.

💵 Compensation & Benefits

💰 Estimated Salary Range:

$88,000 – $121,000 annually
Final pay determined by experience, location, skills, and market factors.
Eligible for discretionary bonus

✔ Benefits Include (From Day One):

Medical, Dental, Vision insurance
401(k) with company match
Employee Stock Purchase Plan (ESPP)
160 hours PTO + Paid Holidays
Paid Parental Leave
Tuition Reimbursement
Flexible Spending Accounts
Commuting & Childcare Benefits
Employee Assistance Program (EAP)
Employee Discount Program
Volunteer Time Off (2 days/year)

🔗 Full Benefits Overview

🛡️ Baxter’s Commitment to Inclusion & Ethics

Baxter is an equal opportunity employer, committed to diversity, equity, and inclusion. We evaluate qualified applicants without regard to:

Race, color, religion, gender
National origin, age, or disability
Sexual orientation or gender identity
Protected veteran or any legally protected status

🔗 Know Your Rights: Workplace Discrimination is Illegal

♿ Reasonable Accommodations

If you need a reasonable accommodation due to a medical condition or disability during the application/interview process:
📩 Request Accommodation Here

⚠️ Recruitment Fraud Notice

Be aware of scams where individuals impersonate Baxter recruiters. Baxter will never request financial information during the hiring process.
🔗 Learn How to Stay Safe

📌 Additional Information

Applicants must be authorized to work in the U.S.
- Baxter does not sponsor visas or provide visa transfers for this role.
Job duties may change at any time with or without notice.
Overtime may be required based on operational demands.

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Quality Lab Senior Supervisor – Night Shift

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