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Function: digital_it
Business unit: Not classified
Location: Raleigh, NC
Work model: Not classified
Seniority: Not classified
Clearance: Not provided
Employment type: Full time
Compensation: Not provided
First seen: 2026-09-15T10:00:57.135Z
Last seen: 2026-10-12T10:00:44.504Z
Requisition: R2962

Latest version

TITLE: Production Investigator/Technical Writer WHO WE ARE Indivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat Opioid Use Disorder (OUD). Our vision is that all patients around the world will have access to evidence-based treatment for OUD, and we are dedicated to transforming OUD from a global human crisis to a recognized and treated chronic disease. Building on its global portfolio of OUD treatments, Indivior has an exploratory pipeline of products designed to expand its heritage in this category. Headquartered in the United States in Richmond, VA, Indivior employs approximately 800 individuals globally. POSITION OVERVIEW The Production Investigator/Technical Writer role is responsible for investigating and reporting on deviations to the manufacturing process, customer complaints on finished product, and other manufacturing problems as assigned. The role is also responsible for creating new documents, updating or doing annual review of documents such as SOPs, Work Instructions, & batch records in the manufacturing area. Will also support surrounding organizations if needed. HOW YOU’LL MAKE AN IMPACT The responsibilities of this role include, but are not limited to, the following: Interact with multiple functional groups to understand the problem & identify root cause(s) Assist in identifying appropriate corrective and/or preventive actions to prevent reoccurrence Create new documents Update SOPs and work instructions Train organization in new documentation updates Implement CAPAs Coordinate and keep track of manufacturing CAPAs/Deviations to make sure the departments are in compliance Assist in audits as a representative from production, present documents and procedures. Assist Operations and Quality Assurance teams to determine the disposition of non-conforming in-process product and determine if a field alert or recall is required for product that has been released WHAT YOU’LL BRING Minimum of an Associate Degree required; Bachelor of Science degree preferred Minimum of two (2) years of experience in Pharmaceutical, Medical Device or Biotech environment writing standard operating procedures, protocols and/or reports required Aseptic and injectable manufacturing experience a plus Good communication (oral, written) and interpersonal skills required. In addition to the minimum qualifications, the employee will demonstrate: Independently investigate pharmaceutical operations and facility nonconformances, identifying any deviations from standards. This includes clearly defining problems, collecting, and organizing existing data, comparing causes to facts, identifying probable root causes, conducting interviews and SME discussions, and determining the best solutions for improvement of manufacturing processes, standard operations procedures (SOPs) and supply chain business practices. Review supporting documentation including batch documentation, ancillary documentation, test results / CoAs, product specifications, training records, SOPs, calibration records, packaging and validation protocols, and other technical documents in support of the investigation. Collaborate with process SMEs, technical, and production personnel to understand events and occurrences. Facilitate meetings with various groups to discuss processes, participate in Kaizen events, and apply formal RCA tools to develop an investigational path for deviations. Present regular updates to the Associate Director, Production. Independently write complex technical reports, describing investigation results and complete according to standard reporting and completion timelines for on time closure. Manage multiple priorities and deadlines independently or as part of a team to meet critical deadlines and company and departmental metrics. Conduct GMP, GDP, SOP, and awareness training as needed for deviation resolution. Assist with revision to SOPs pertaining to component preparation, compounding, filling, and stoppering of sterile vials, lyophilizing, capping, and inspection of product based on investigation findings. Obtain and maintain aseptic gowning qualification. HOW WE INVEST IN OUR PEOPLE Indivior is committed to providing a culture driven by guiding principles and top-tier benefits that match the importance of the work we do. The Indivior experience includes: Competitive PTO plus company closure from December 24th- January 1st Eligible to participate in Indivior’s bonus program, based on company and individual performance Comprehensive Medical, Dental, Vision, Life and Disability coverage Health, Dependent Care and Limited Purpose Flex Spending and HSA options Adoption assistance Tuition reimbursement Concierge/personal assistance services Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage Wellness programs as well as other discounts and perks OUR SHARED RESPONSIBILITY FOR ETHICAL CONDUCT Indivior is committed to maintaining a workplace where employees are committed to compliance and feel comfortable raising concerns about potential violations of policies or unethical behavior. Employee Obligations: Have unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure Risk IQ: Know what policies apply to your role and function and adhere to them. Speak Up: If you see something, say something. Manager Obligations: Have unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure Reinforce risk awareness with your team, with accountability and oversight for ongoing review and mitigation. Model and reinforce a Speak Up culture on your team. 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. Want to learn more? Connect with us at www.indivior.com or follow us at www.linkedin.com/company/Indivior. #LI-AC1

Content hash: 11ee61573db4588d4f15a9c98d1db902371a3aa97f5f1210075163225c122bec

Derived classifications

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        "Tuition reimbursement Concierge/personal assistance services Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage Wellness programs as well as other discounts"
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    }
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}

Version history

2 retained

Version 22026-09-23T10:01:02.417Z{"description":{"after":{"description_text":"TITLE:\nProduction Investigator/Technical Writer\nWHO WE ARE\nIndivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat Opioid Use Disorder (OUD). Our vision is that all patients around the world will have access to evidence-based treatment for OUD, and we are dedicated to transforming OUD from a global human crisis to a recognized and treated chronic disease. Building on its global portfolio of OUD treatments, Indivior has an exploratory pipeline of products designed to expand its heritage in this category. Headquartered in the United States in Richmond, VA, Indivior employs approximately 800 individuals globally.\nPOSITION OVERVIEW\nThe Production Investigator/Technical Writer role is responsible for investigating and reporting on deviations to the manufacturing process, customer complaints on finished product, and other manufacturing problems as assigned. The role is also responsible for creating new documents, updating or doing annual review of documents such as SOPs, Work Instructions, & batch records in the manufacturing area. Will also support surrounding organizations if needed.\nHOW YOU’LL MAKE AN IMPACT\nThe responsibilities of this role include, but are not limited to, the following:\nInteract with multiple functional groups to understand the problem & identify root cause(s)\nAssist in identifying appropriate corrective and/or preventive actions to prevent reoccurrence\nCreate new documents\nUpdate SOPs and work instructions\nTrain organization in new documentation updates\nImplement CAPAs\nCoordinate and keep track of manufacturing CAPAs/Deviations to make sure the departments are in compliance\nAssist in audits as a representative from production, present documents and procedures.\nAssist Operations and Quality Assurance teams to determine the disposition of non-conforming in-process product and determine if a field alert or recall is required for product that has been released\nWHAT YOU’LL BRING\nMinimum of an Associate Degree required; Bachelor of Science degree preferred\nMinimum of two (2) years of experience in Pharmaceutical, Medical Device or Biotech environment writing standard operating procedures, protocols and/or reports required\nAseptic and injectable manufacturing experience a plus\nGood communication (oral, written) and interpersonal skills required.\nIn addition to the minimum qualifications, the employee will demonstrate:\nIndependently investigate pharmaceutical operations and facility nonconformances, identifying any deviations from standards. This includes clearly defining problems, collecting, and organizing existing data, comparing causes to facts, identifying probable root causes, conducting interviews and SME discussions, and determining the best solutions for improvement of manufacturing processes, standard operations procedures (SOPs) and supply chain business practices.\nReview supporting documentation including batch documentation, ancillary documentation, test results / CoAs, product specifications, training records, SOPs, calibration records, packaging and validation protocols, and other technical documents in support of the investigation.\nCollaborate with process SMEs, technical, and production personnel to understand events and occurrences. Facilitate meetings with various groups to discuss processes, participate in Kaizen events, and apply formal RCA tools to develop an investigational path for deviations. Present regular updates to the Associate Director, Production.\nIndependently write complex technical reports, describing investigation results and complete according to standard reporting and completion timelines for on time closure. Manage multiple priorities and deadlines independently or as part of a team to meet critical deadlines and company and departmental metrics. Conduct GMP, GDP, SOP, and awareness training as needed for deviation resolution.\nAssist with revision to SOPs pertaining to component preparation, compounding, filling, and stoppering of sterile vials, lyophilizing, capping, and inspection of product based on investigation findings.\nObtain and maintain aseptic gowning qualification.\nHOW WE INVEST IN OUR PEOPLE\nIndivior is committed to providing a culture driven by guiding principles and top-tier benefits that match the importance of the work we do. The Indivior experience includes:\nCompetitive PTO plus company closure from December 24th- January 1st\nEligible to participate in Indivior’s bonus program, based on company and individual performance\nComprehensive Medical, Dental, Vision, Life and Disability coverage\nHealth, Dependent Care and Limited Purpose Flex Spending and HSA options\nAdoption assistance\nTuition reimbursement\nConcierge/personal assistance services\nVoluntary benefits including Legal, Pet Insurance and Critical Illness coverage\nWellness programs as well as other discounts and perks\nOUR SHARED RESPONSIBILITY FOR ETHICAL CONDUCT\nIndivior is committed to maintaining a workplace where employees are committed to compliance and feel comfortable raising concerns about potential violations of policies or unethical behavior.\nEmployee Obligations:\nHave unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure\nRisk IQ: Know what policies apply to your role and function and adhere to them.\nSpeak Up: If you see something, say something.\nManager Obligations:\nHave unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure\nReinforce risk awareness with your team, with accountability and oversight for ongoing review and mitigation.\nModel and reinforce a Speak Up culture on your team.\nEQUAL EMPLOYMENT OPPORTUNITY\nEOE/Minorities/Females/Vet/Disabled\nare encouraged to apply!\nThe duties and responsibilities\nidentified\nin this position description are considered essential but are not limited to only those outlined.\nThe\nemployee\nmay perform other functions that may be assigned.\nManagement\nretains\nthe discretion to add or change the duties of this\nposition at any time.\nWant to learn more? Connect with us at\nwww.indivior.com\nor follow us at\nwww.linkedin.com/company/Indivior.\n#LI-AC1"},"before":{"description_text":"TITLE:\nProduction Investigator/Technical Writer\nWHO WE ARE\nIndivior is a global pharmaceutical company working to help change patients' lives by developing medicines to treat Opioid Use Disorder (OUD). Our vision is that all patients around the world will have access to evidence-based treatment for OUD, and we are dedicated to transforming OUD from a global human crisis to a recognized and treated chronic disease. Building on its global portfolio of OUD treatments, Indivior has an exploratory pipeline of products designed to expand its heritage in this category. Headquartered in the United States in Richmond, VA, Indivior employs approximately 800 individuals globally.\nPOSITION OVERVIEW\nThe Production Investigator/Technical Writer role is responsible for investigating and reporting on deviations to the manufacturing process, customer complaints on finished product, and other manufacturing problems as assigned. The role is also responsible for creating new documents, updating or doing annual review of documents such as SOPs, Work Instructions, & batch records in the manufacturing area. Will also support surrounding organizations if needed.\nHOW YOU’LL MAKE AN IMPACT\nThe responsibilities of this role include, but are not limited to, the following:\nInteract with multiple functional groups to understand the problem & identify root cause(s)\nAssist in identifying appropriate corrective and/or preventive actions to prevent reoccurrence\nCreate new documents\nUpdate SOPs and work instructions\nTrain organization in new documentation updates\nImplement CAPAs\nCoordinate and keep track of manufacturing CAPAs/Deviations to make sure the departments are in compliance\nAssist in audits as a representative from production, present documents and procedures.\nAssist Operations and Quality Assurance teams to determine the disposition of non-conforming in-process product and determine if a field alert or recall is required for product that has been released\nWHAT YOU’LL BRING\nMinimum of an Associate Degree required; Bachelor of Science degree preferred\nMinimum of two (2) years of experience in Pharmaceutical, Medical Device or Biotech environment writing standard operating procedures, protocols and/or reports required\nAseptic and injectable manufacturing experience a plus\nGood communication (oral, written) and interpersonal skills required.\nIn addition to the minimum qualifications, the employee will demonstrate:\nIndependently investigate pharmaceutical operations and facility nonconformances, identifying any deviations from standards. This includes clearly defining problems, collecting, and organizing existing data, comparing causes to facts, identifying probable root causes, conducting interviews and SME discussions, and determining the best solutions for improvement of manufacturing processes, standard operations procedures (SOPs) and supply chain business practices.\nReview supporting documentation including batch documentation, ancillary documentation, test results / CoAs, product specifications, training records, SOPs, calibration records, packaging and validation protocols, and other technical documents in support of the investigation.\nCollaborate with process SMEs, technical, and production personnel to understand events and occurrences. Facilitate meetings with various groups to discuss processes, participate in Kaizen events, and apply formal RCA tools to develop an investigational path for deviations. Present regular updates to the Associate Director, Production.\nIndependently write complex technical reports, describing investigation results and complete according to standard reporting and completion timelines for on time closure. Manage multiple priorities and deadlines independently or as part of a team to meet critical deadlines and company and departmental metrics. Conduct GMP, GDP, SOP, and awareness training as needed for deviation resolution.\nAssist with revision to SOPs pertaining to component preparation, compounding, filling, and stoppering of sterile vials, lyophilizing, capping, and inspection of product based on investigation findings.\nObtain and maintain aseptic gowning qualification.\nHOW WE INVEST IN OUR PEOPLE\nIndivior is committed to providing a culture driven by guiding principles and top-tier benefits that match the importance of the work we do. The Indivior experience includes:\nCompetitive PTO plus company closure from December 24th- January 1st\nEligible to participate in Indivior’s bonus program, based on company and individual performance\nEligible to receive a yearly grant as part of Indivior’s Long-Term Incentive Plan\n401(k) and Profit-Sharing Plan- Company match\nU.S. Employee Stock Purchase Plan- 15% Discount\nComprehensive Medical, Dental, Vision, Life and Disability coverage\nHealth, Dependent Care and Limited Purpose Flex Spending and HSA options\nAdoption assistance\nTuition reimbursement\nConcierge/personal assistance services\nVoluntary benefits including Legal, Pet Insurance and Critical Illness coverage\nWellness programs as well as other discounts and perks\nOUR SHARED RESPONSIBILITY FOR ETHICAL CONDUCT\nIndivior is committed to maintaining a workplace where employees are committed to compliance and feel comfortable raising concerns about potential violations of policies or unethical behavior.\nEmployee Obligations:\nHave unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure\nRisk IQ: Know what policies apply to your role and function and adhere to them.\nSpeak Up: If you see something, say something.\nManager Obligations:\nHave unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure\nReinforce risk awareness with your team, with accountability and oversight for ongoing review and mitigation.\nModel and reinforce a Speak Up culture on your team.\nEQUAL EMPLOYMENT OPPORTUNITY\nEOE/Minorities/Females/Vet/Disabled\nare encouraged to apply!\nThe duties and responsibilities\nidentified\nin this position description are considered essential but are not limited to only those outlined.\nThe\nemployee\nmay perform other functions that may be assigned.\nManagement\nretains\nthe discretion to add or change the duties of this\nposition at any time.\nWant to learn more? Connect with us at\nwww.indivior.com\nor follow us at\nwww.linkedin.com/company/Indivior.\n#LI-AC1"}},"source_dates":{"after":{"posting_date":"2026-09-22","valid_through":null},"before":{"posting_date":"2026-09-14","valid_through":null}}}

{
  "added": [
    "The Indivior experience includes: Competitive PTO plus company closure from December 24th- January 1st Eligible to participate in Indivior’s bonus program, based on company and individual performance Comprehensive Medical, Dental, Vision, Life and Disability coverage Health, Dependent Care and Limited Purpose Flex Spending and HSA options Adoption assistance Tuition reimbursement Concierge/personal assistance services Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage Wellness programs as well as other discounts and perks OUR SHARED RESPONSIBILITY FOR ETHICAL CONDUCT Indivior is committed to maintaining a workplace where employees are committed to compliance and feel comfortable raising concerns about potential violations of policies or unethical behavior."
  ],
  "removed": [
    "The Indivior experience includes: Competitive PTO plus company closure from December 24th- January 1st Eligible to participate in Indivior’s bonus program, based on company and individual performance Eligible to receive a yearly grant as part of Indivior’s Long-Term Incentive Plan 401(k) and Profit-Sharing Plan- Company match U.S.",
    "Employee Stock Purchase Plan- 15% Discount Comprehensive Medical, Dental, Vision, Life and Disability coverage Health, Dependent Care and Limited Purpose Flex Spending and HSA options Adoption assistance Tuition reimbursement Concierge/personal assistance services Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage Wellness programs as well as other discounts and perks OUR SHARED RESPONSIBILITY FOR ETHICAL CONDUCT Indivior is committed to maintaining a workplace where employees are committed to compliance and feel comfortable raising concerns about potential violations of policies or unethical behavior."
  ]
}

Version 12026-09-15T10:00:57.135ZInitial version