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Quality Lab Senior Supervisor – Night Shift

5 years years
$88,000 – $121,000 annually
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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