Home › Companies › Hbap Fa Us1 Oraclecloud Com CX 1 › QC Analyst III/IV - Environmental Monitoring
QC Analyst III/IV - Environmental Monitoring
Hbap Fa Us1 Oraclecloud Com CX 1 · Wilmington, OH, United States · On Site · Active · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Hbap Fa Us1 Oraclecloud Com CX 1 |
| Title | QC Analyst III/IV - Environmental Monitoring |
| Normalized title | - |
| Department / team | Quality |
| Location | Wilmington, OH, United States |
| Work model | On Site |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-05-26 / 2026-05-31 |
| Changed / last seen | 2026-06-03 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Hbap Fa Us1 Oraclecloud Com CX 1. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Wilmington. | Open |
| Department jobs | Active postings in Quality. | Open |
| Work model jobs | Active On Site postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Hbap Fa Us1 Oraclecloud Com CX 1 |
| Source | c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85 |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
POSITION SUMMARY
The QC Microbiology Analyst will be responsible for performing functions including environmental monitoring, utilities monitoring, and testing in a facility that manufactures sterile products and tablets in a GMP environment.
MAJOR RESPONSIBILITIES
Major Responsibilities
Percentage of time spent on each responsibility
Prepare documents such as change controls, risk assessments, SOP’s, protocols, final reports and support of discrepancies
35%
Review of risk assessments, deviations, protocols, change controls, and other technical documents from internal and external departments
20%
Perform training of manufacturing and EM personnel
15%
Perform environmental monitoring in aseptic, classified, and controlled areas (routine, batch, quarterly EM). Direct support of the manufacturing schedule will be required, which may include over time, weekend or shift work, and holidays
10%
Perform utilities monitoring (WFI, CLST, PW, RO, CAIR, NIT, PWTR) and testing (Endotoxin, TOC, Conductivity, Nitrates, Bioburden)
10%
Enumerate organisms for environmental monitoring and utility samples.
5%
Perform classified area walkthroughs and production observations
5%
QUALIFICATIONS
Technical writing skills which require minimal guidance from management
Ability to work hard and contribute to an enjoyable working environment
Ability to work safely; seek out and encourage safe practices
Gowning in an aseptic environment
Self-starter that takes initiative to perform work with minimal supervision
Maintain documentation in accordance with GMP including timely recording of information
Pays attention to detail and ensures high quality work Ability to cope with a rapidly changing work environment
Commitment to teamwork
Willingness to learn new things
Commitment to continuous improvement in all areas
Effective communication with co-workers, other departments, and management
Lead training on environmental monitoring, utilities, gowning, or aseptic practices
Works closely with manufacturing for training, walkthroughs, and sample coordination
Able to come up with solutions and resolve issues
Audit support as needed
Act as department representative in meetings
EDUCATION: Bachelors/Associates in Biology (or related field) or high school diploma with additional experience being substituted for a degree
EXPERIENCE: QC Analyst III - 6+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience.
QC Analyst IV - 8+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience.
WORKING CONDITIONS
The successful employee will have the ability to function in a microbiological laboratory and manufacturing environment. The employee should have no inhibitions regarding safely handling microorganisms present in the laboratory and no health conditions/allergies that would prevent them from doing so or conditions which would prevent them from aseptically gowning. Aseptic gowning must be able to be maintained including an annual requalification. Employee must be able to pass a vision exam prior to employment and annually thereafter. The employee will be required to participate in an on call schedule for various shift, holiday, or weekend work as needed.
PHYSICAL REQUIREMENTS
Prolonged periods of sitting or standing.
Occasional periods of repetitive motion
Walking, lifting, pushing and pulling carts, reaching, climbing, and bending may all be required.
Steel toe shoes, scrubs, safety glasses, and other PPE equipment must be worn based on job being performed.
Makeup and Jewelry will not be permitted for work in classified areas or other areas as necessary
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.
#LI-RS1
#LI-Onsite
Company
Why join Team Alkermes?
Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.
We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.
Full job record
| Job ID | f61ae7b8669449d18803662ef41cf705aaab9f6d |
| Org ID | d831e3c2-6a79-44af-a2cf-903b76ab4731 |
| Source ID | c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85 |
| Board ID | c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85 |
| Provider | oracle_hcm |
| Provider Job Key | 13996 |
| Title | QC Analyst III/IV - Environmental Monitoring |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Wilmington, OH, United States |
| Department | Quality |
| Team | — |
| Employment Type | full_time |
| Workplace Type | on_site |
| Remote Policy | — |
| Country | United States |
| Region | OH |
| City | Wilmington |
| Salary Raw | Description POSITION SUMMARY The QC Microbiology Analyst will be responsible for performing functions including environmental monitoring, utilities monitoring, and testing in a facility that manufactures sterile products and tablets in a GMP environment. MAJOR RESPONSIBILITIES Major Responsibilities Percentage of time spent on each responsibility Prepare documents such as change controls, risk assessments, SOP’s, protocols, final reports and support of discrepancies 35% Review of risk assessments, deviations, protocols, change controls, and other technical documents from internal and external departments 20% Perform training of manufacturing and EM personnel 15% Perform environmental monitoring in aseptic, classified, and controlled areas (routine, batch, quarterly EM). Direct support of the manufacturing schedule will be required, which may include over time, weekend or shift work, and holidays 10% Perform utilities monitoring (WFI, CLST, PW, RO, CAIR, NIT, PWTR) and testing (Endotoxin, TOC, Conductivity, Nitrates, Bioburden) 10% Enumerate organisms for environmental monitoring and utility samples. 5% Perform classified area walkthroughs and production observations 5% QUALIFICATIONS Technical writing skills which require minimal guidance from management Ability to work hard and contribute to an enjoyable working environment Ability to work safely; seek out and encourage safe practices Gowning in an aseptic environment Self-starter that takes initiative to perform work with minimal supervision Maintain documentation in accordance with GMP including timely recording of information Pays attention to detail and ensures high quality work Ability to cope with a rapidly changing work environment Commitment to teamwork Willingness to learn new things Commitment to continuous improvement in all areas Effective communication with co-workers, other departments, and management Lead training on environmental monitoring, utilities, gowning, or aseptic practices Works closely with manufacturing for training, walkthroughs, and sample coordination Able to come up with solutions and resolve issues Audit support as needed Act as department representative in meetings EDUCATION: Bachelors/Associates in Biology (or related field) or high school diploma with additional experience being substituted for a degree EXPERIENCE: QC Analyst III - 6+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience. QC Analyst IV - 8+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience. WORKING CONDITIONS The successful employee will have the ability to function in a microbiological laboratory and manufacturing environment. The employee should have no inhibitions regarding safely handling microorganisms present in the laboratory and no health conditions/allergies that would prevent them from doing so or conditions which would prevent them from aseptically gowning. Aseptic gowning must be able to be maintained including an annual requalification. Employee must be able to pass a vision exam prior to employment and annually thereafter. The employee will be required to participate in an on call schedule for various shift, holiday, or weekend work as needed. PHYSICAL REQUIREMENTS Prolonged periods of sitting or standing. Occasional periods of repetitive motion Walking, lifting, pushing and pulling carts, reaching, climbing, and bending may all be required. Steel toe shoes, scrubs, safety glasses, and other PPE equipment must be worn based on job being performed. Makeup and Jewelry will not be permitted for work in classified areas or other areas as necessary Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law. #LI-RS1 #LI-Onsite Company Why join Team Alkermes? Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer. |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://hbap.fa.us1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/13996 |
| Apply URL | https://hbap.fa.us1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/13996 |
| First Seen At | 2026-05-31 18:10:58Z |
| Last Seen At | 2026-06-06 11:11:22Z |
| Last Checked At | 2026-06-06 11:11:22Z |
| Last Changed At | 2026-06-03 11:55:41Z |
| Inactive At | — |
| Source Posted At | 2026-05-26 14:42:52Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=hbap.fa.us1.oraclecloud.com|CX_1/date=2026-06-06/2026-06-06T11-11-16-535Z-17c3bce20012c43cd6dd6a420957faaa6610803a2a194c866b3ecf324160566d.json |
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"ExternalDescriptionStr": "<p style=\"line-height: normal; margin-bottom: 0in;\">POSITION SUMMARY</p><p style=\"line-height: normal; margin-bottom: 0in;\"> </p><figure class=\"table\"><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"671\" style=\"border-collapse: collapse; border: none; margin-left: 5.4pt; width: 503.05pt;\"><tbody><tr style=\"height: 57.55pt;\"><td width=\"671\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 57.55pt; padding: 0in 5.4pt; width: 503.05pt;\"><p style=\"line-height: normal; margin-bottom: 0in; text-align: justify;\"> </p><p style=\"line-height: normal; margin-bottom: 0in; text-align: justify;\">The QC Microbiology Analyst will be responsible for performing functions including environmental monitoring, utilities monitoring, and testing in a facility that manufactures sterile products and tablets in a GMP environment.</p></td></tr></tbody></table></figure><p style=\"line-height: normal; margin-bottom: 0in;\"> </p><p style=\"line-height: normal; margin-bottom: 0in;\">MAJOR RESPONSIBILITIES</p><p style=\"line-height: normal; margin-bottom: 0in;\"> </p><figure class=\"table\"><table border=\"1\" cellspacing=\"0\" cellpadding=\"0\" width=\"672\" style=\"border-collapse: collapse; border: none; margin-left: 5.4pt; width: 7in;\"><tbody><tr style=\"height: 12.85pt;\"><td width=\"540\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 12.85pt; padding: 0in 5.4pt; width: 405pt;\"><p style=\"line-height: normal; margin-bottom: 0in; text-align: center;\">Major Responsibilities</p></td><td width=\"132\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 12.85pt; padding: 0in 5.4pt; width: 99pt;\"><p style=\"line-height: normal; margin-bottom: 0in;\">Percentage of time spent on each responsibility</p></td></tr><tr style=\"height: 13.85pt;\"><td width=\"540\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 13.85pt; padding: 0in 5.4pt; width: 405pt;\"><p style=\"line-height: normal; margin: 0in 15pt 0in 0in; text-align: justify;\">Prepare documents such as change controls, risk assessments, SOP’s, protocols, final reports and support of discrepancies</p></td><td width=\"132\" valign=\"top\" style=\"border-bottom: 1pt solid windowtext; border-left: none; border-right: 1pt solid windowtext; border-top: none; height: 13.85pt; padding: 0in 5.4pt; width: 99pt;\"><p style=\"line-height: normal; margin-bottom: 0in; text-align: center;\">35%</p></td></tr><tr style=\"height: 12.85pt;\"><td width=\"540\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 12.85pt; padding: 0in 5.4pt; width: 405pt;\"><p style=\"line-height: normal; margin: 0in 15pt 0in 0in; text-align: justify;\">Review of risk assessments, deviations, protocols, change controls, and other technical documents from internal and external departments</p></td><td width=\"132\" valign=\"top\" style=\"border-bottom: 1pt solid windowtext; border-left: none; border-right: 1pt solid windowtext; border-top: none; height: 12.85pt; padding: 0in 5.4pt; width: 99pt;\"><p style=\"line-height: normal; margin-bottom: 0in; text-align: center;\">20%</p></td></tr><tr style=\"height: 12.85pt;\"><td width=\"540\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 12.85pt; padding: 0in 5.4pt; width: 405pt;\"><p style=\"line-height: normal; margin: 0in 15pt 0in 0in; text-align: justify;\">Perform training of manufacturing and EM personnel</p></td><td width=\"132\" valign=\"top\" style=\"border-bottom: 1pt solid windowtext; border-left: none; border-right: 1pt solid windowtext; border-top: none; height: 12.85pt; padding: 0in 5.4pt; width: 99pt;\"><p style=\"line-height: normal; margin-bottom: 0in; text-align: center;\">15%</p></td></tr><tr style=\"height: 12.85pt;\"><td width=\"540\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 12.85pt; padding: 0in 5.4pt; width: 405pt;\"><p style=\"line-height: normal; margin: 0in 15pt 0in 0in; text-align: justify;\">Perform environmental monitoring in aseptic, classified, and controlled areas (routine, batch, quarterly EM). Direct support of the manufacturing schedule will be required, which may include over time, weekend or shift work, and holidays</p></td><td width=\"132\" valign=\"top\" style=\"border-bottom: 1pt solid windowtext; border-left: none; border-right: 1pt solid windowtext; border-top: none; height: 12.85pt; padding: 0in 5.4pt; width: 99pt;\"><p style=\"line-height: normal; margin-bottom: 0in; text-align: center;\">10%</p></td></tr><tr style=\"height: 12.85pt;\"><td width=\"540\" valign=\"top\" style=\"border: 1pt solid windowtext; height: 12.85pt; padding: 0in 5.4pt; width: 405pt;\"><p style=\"line-height: normal; margin: 0in 15pt 0in -0.9pt; text-align: justify;\">Perform utilities monitoring (WFI, CLST, PW, RO, CAIR, NIT, PWTR) and testing (Endotoxin, TOC, Conductivity, Nitrates, Bioburden)</p></td><td width=\"132\" valign=\"top\" style=\"border-bottom: 1pt solid windowtext; border-left: none; border-right: 1pt solid windowtext; border-top: none; height: 12.85pt; padding: 0in 5.4pt; width: 99pt;\"><p style=\"line-height: normal; 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margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\">Self-starter that takes initiative to perform work with minimal supervision </p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Maintain documentation in accordance with GMP including timely recording of information</p></li><li class=\"ortl-align-justify\">Pays attention to detail and ensures high quality work</li><li><p style=\"line-height: normal; margin-bottom: 0in;\">Ability to cope with a rapidly changing work environment</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Commitment to teamwork</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Willingness to learn new things</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Commitment to continuous improvement in all areas</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Effective communication with co-workers, other departments, and management</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Lead training on environmental monitoring, utilities, gowning, or aseptic practices </p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Works closely with manufacturing for training, walkthroughs, and sample coordination</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Able to come up with solutions and resolve issues </p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Audit support as needed</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\">Act as department representative in meetings </p></li></ul><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 15pt; margin-top: 0in;\"> </p><p style=\"line-height: normal; margin-bottom: 0in;\"> </p><p>EDUCATION: Bachelors/Associates in Biology (or related field) or high school diploma with additional experience being substituted for a degree </p><p>EXPERIENCE: QC Analyst III - 6+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience.</p><p>QC Analyst IV - 8+ years of cGMP laboratory and/or Pharmaceutical Quality experience. Some college education may be substituted with additional years of relevant work experience.</p><p style=\"line-height: normal; margin-bottom: 0in;\">WORKING CONDITIONS</p><ul style=\"list-style-type: disc;\"><li>The successful employee will have the ability to function in a microbiological laboratory and manufacturing environment. The employee should have no inhibitions regarding safely handling microorganisms present in the laboratory and no health conditions/allergies that would prevent them from doing so or conditions which would prevent them from aseptically gowning.</li><li>Aseptic gowning must be able to be maintained including an annual requalification.</li><li>Employee must be able to pass a vision exam prior to employment and annually thereafter.</li><li><p>The employee will be required to participate in an on call schedule for various shift, holiday, or weekend work as needed.</p><p> </p></li></ul><p style=\"line-height: normal; margin-bottom: 0in;\"> </p><p style=\"line-height: normal; margin-bottom: 0in;\">PHYSICAL REQUIREMENTS</p><ul style=\"list-style-type: disc; padding-left: 24px;\"><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\">Prolonged periods of sitting or standing.</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\">Occasional periods of repetitive motion</p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\">Walking, lifting, pushing and pulling carts, reaching, climbing, and bending may all be required. </p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\">Steel toe shoes, scrubs, safety glasses, and other PPE equipment must be worn based on job being performed. </p></li><li class=\"ortl-align-justify\"><p style=\"line-height: normal; margin-bottom: 0in; margin-right: 0in; margin-top: 0in;\">Makeup and Jewelry will not be permitted for work in classified areas or other areas as necessary</p></li></ul><p style=\"line-height: normal; margin-bottom: 0in;\"> </p><p>Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.</p><p> </p><p>#LI-RS1</p><p>#LI-Onsite</p>",
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"CorporateDescriptionStr": "<div>\n <div>\n <p><b>Why join Team Alkermes?</b></p>\n <p>Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders.</p>\n <p></p>\n <p>We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. </p>\n </div>\n <div>\n <p>Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.</p>\n </div>\n</div>",
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