Production Supervisor - 2nd Shift

Indivior PLC; Raleigh (NC); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Competitive PTO

401(k) with company match

Employee Stock Purchase Plan

Job summary

Indivior PLC in Raleigh, NC is seeking a Production Supervisor for the 2nd Shift. This role involves ensuring safety, quality, and performance in the prep and compounding areas, while managing day-to-day production activities.

The ideal candidate will have demonstrated leadership in a regulated industry, with substantial experience in cGMP manufacturing preferred. Benefits include 401(k) with company match, comprehensive health coverage, and more.

Qualifications

• Minimum 5 years of experience in a regulated industry.
• Minimum 3 years of supervisory experience preferred.
• Experience in cGMP manufacturing or clean-room production preferred.

Responsibilities

• Ensure operational areas comply with cGMP.
• Manage day-to-day activities of the production area.
• Investigate deviations and implement corrective actions.

Skills

Leadership and supervisory skills

Analytical reasoning

Computer proficiency

Technical writing

Mathematical skills

Job description

Position Overview

Production Supervisor – 2nd Shift at Indivior. Responsible for the safety, quality, and performance of the prep, compounding, filling, and inspection areas, working in both aseptic and non‑aseptic environments.

Key Responsibilities

• Ensure operational areas comply with cGMP and implement continuous improvement systems.
• Oversee accurate documentation and close‑out of batch records.
• Manage day‑to‑day activities of the production area.
• Develop, review, and revise SOPs for prep, compounding, and filling.
• Drive operational improvement and trend key performance indicators.
• Lead and develop the team; provide coaching and cross‑functional leadership.
• Investigate deviations, root‑cause analysis, and implement corrective actions.
• Review batch documentation, test results, specifications, training, and other technical records.
• Assist with CAPA investigations and rollout of finalized actions.
• Serve as subject‑matter expert during internal and external audits; lead audit presentations.
• Lead Tier 1 meetings and participate in Tier 2 meetings.
• Build a self‑sufficient team capable of independent operations.
• Cover for peers and manager as required.

Qualifications

• Demonstrated leadership and supervisory skills.
• Minimum 5 years of experience in a regulated industry.
• Minimum 3 years of supervisory experience (preferred).
• Experience in cGMP manufacturing or clean‑room production (preferred).
• Pre‑filled syringe experience preferred.
• Strong analytical reasoning and root‑cause analysis skills.
• Excellent math and calculating skills.
• Computer proficiency.
• Excellent technical writing and instruction interpretation.
• Ability to apply continuous improvement and operational excellence concepts.

Benefits

• Competitive PTO and company closure days.
• Eligibility for bonus and long‑term incentive plans.
• 401(k) with company match and profit‑sharing plan.
• Employee Stock Purchase Plan with discount.
• Comprehensive medical, dental, vision, life, and disability coverage.
• Health, dependent‑care, and limited‑purpose HSA/Flex Spending options.
• Adoption assistance and tuition reimbursement.
• Legal, pet, critical illness, and other voluntary benefits.
• Wellness programs and additional benefits.

EQUAL EMPLOYMENT OPPORTUNITY: EOE/Minorities/Females/Vet/Disabled are encouraged to apply! The duties and responsibilities identified in this position description are considered essential but are not limited to only those outlined. The employee may perform other functions that may be assigned. Management retains the discretion to add or change the duties of this position at any time.