Production Supervisor
$100k - $115k
Senior
Raleigh, NC, USA
In Person
Manufacturing & Production Operations
About the job
Requirements
- Demonstrated leadership and supervisory skills.
- At least five years of experience in a regulated industry.
- Ability to apply analytical reasoning and root cause analysis to solve problems.
- Strong mathematics and calculation skills.
- Computer skills.
- Ability to read, understand, interpret, and implement technical writing and instructions, and to solve problems in a fast-paced environment.
- Ability to become certified on all curricula in the operational area to understand the process, help improve it, and provide coverage for breaks and vacancies.
- Ability to investigate pharmaceutical operations and facility nonconformances independently, identify deviations from standards, define problems, collect and organize existing data, compare causes to facts, identify probable root causes, conduct interviews and subject-matter expert discussions, and determine solutions to improve manufacturing processes, standard operating procedures, and supply chain business practices.
- Ability to review batch and ancillary documentation, test results and certificates of analysis, product specifications, training records, standard operating procedures, calibration records, packaging and validation protocols, and other technical documents.
- Ability to assist with deviation and corrective and preventive action investigations, understand the process, and take over and finalize an investigation when needed.
- Ability to serve as the subject-matter expert during internal and external audits, lead presentations, and present to audit teams.
- Ability to build a self-sufficient team that can work independently with minimal oversight.
- Unquestionable ethics and integrity, including willingness to uphold these principles under significant pressure.
- Knowledge of policies applicable to the role and function and ability to adhere to them.
- Willingness to raise concerns about potential violations of policies or unethical behavior.
Responsibilities
- Oversee operational areas for current Good Manufacturing Practice compliance and establish systems that support continuous improvement of procedures and quality.
- Ensure timely and accurate documentation and closeout of batch records.
- Manage the day-to-day activities of the operational area.
- Develop and review standard operating procedures pertaining to preparation, compounding, and filling.
- Drive continued improvement in operational areas.
- Trend key performance indicators and take appropriate action.
- Develop and manage personnel.
- Lead cross-functional teams to resolve urgent production issues and implement improvements.
- Work with the operational team to improve key performance indicators and other trends or tasks independently.
- Assist with revisions to standard operating procedures as a subject-matter expert in the operating area.
- Lead Tier 1 meetings and participate in Tier 2 meetings.
- Cover for peers and the manager when needed.
- Reinforce risk awareness with the team and oversee ongoing review and mitigation.
- Model and reinforce a culture in which employees speak up.
Desired Qualifications
- At least three years of related supervisory experience.
- Experience in current Good Manufacturing Practice manufacturing or a cleanroom production environment.
- Prefilled syringe experience.
About the company
Indivior focuses on developing medicines for substance use disorders and serious mental illnesses. Its products are prescription pharmaceutical treatments, brought to market after research and development, and sold through healthcare professionals to patients worldwide. The company’s approach centers on patient safety, with ongoing monitoring and reporting of adverse events to ensure high-quality therapies. Compared with competitors, Indivior emphasizes targeted medicines for addiction and mental health, combining scientific R&D with a global commercialization presence to address critical healthcare needs. Its goal is to create sustainable value by improving patient outcomes and addressing unmet medical needs in global health.
Company Size
501-1,000
Company Stage
IPO
Headquarters
Bon Air, Virginia
Founded
2014
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Simplify's Take
What believers are saying
- Q1 2026 revenue rose 19% to $317 million, driven by SUBLOCADE's 32% growth.
- Indivior raised 2026 guidance to $1.215-$1.285 billion and EBITDA to $620-$660 million.
- The $1 billion special dividend and $125 million synergies signal disciplined capital returns and cost cuts.
What critics are saying
- Indivior ended its Addex PAM collaboration on September 25, 2026, shrinking pipeline optionality.
- Management killed INDV-6001 and INDV-2000 in 2026, exposing thin internal pipeline execution.
- SUBLOCADE concentration makes any payer squeeze, safety event, or generic threat existential.
What makes Indivior unique
- SUBLOCADE dominates long-acting buprenorphine, with over 500,000 patients prescribed by Q1 2026.
- Indivior owns a rare addiction-focused commercial platform with global reimbursement and prescriber relationships.
- The Supernus merger creates a broader CNS franchise with 11 marketed medicines and $2.2 billion revenue.
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Benefits
- Paid Vacation
- Paid Holidays
- Paid Sick Leave
- Flexible Work Hours
- Remote Work Options
- Health Insurance
- Dental Insurance
- Vision Insurance
- Life Insurance
- Disability Insurance
- Health Savings Account/Flexible Spending Account
- Adoption Assistance