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HomeCompaniesIboijb Fa Ocs Oraclecloud Com CX 1003QA Team Lead

QA Team Lead

Iboijb Fa Ocs Oraclecloud Com CX 1003 · East Windsor, NJ, United States; ANI East Windsor Facility NJ, Trenton, NJ, US · On Site · Active · $80,000–$100,000 / year · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIboijb Fa Ocs Oraclecloud Com CX 1003
TitleQA Team Lead
Normalized title-
Department / team-
LocationEast Windsor, NJ, United States
Work modelOn Site
Employment typeFull Time
Salary$80,000–$100,000 / year
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-06-02 / 2026-06-03
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from Iboijb Fa Ocs Oraclecloud Com CX 1003.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Oracle Recruiting Cloud / Fusion HCM.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in East Windsor.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyIboijb Fa Ocs Oraclecloud Com CX 1003
Source090db789-6574-433c-818a-bcb676318fb8
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description About Us Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients' lives through the manufacturing and distribution of high-quality pharmaceutical products. With a diverse portfolio of generic and branded pharmaceuticals, ANI is a trusted partner for healthcare providers, pharmacists, and patients alike. At ANI Pharmaceuticals, there are opportunities to contribute to our purpose every day. We value authenticity, knowledge, and hard work, and we strive to celebrate our employees in a positive environment. Our culture empowers everyone to be successful and apply their full potential. About the Role This position is responsible for supporting Manufacturing and Packaging Operations to ensure compliance with applicable procedures, GMP requirements, and regulatory standards. In addition to individual contributor responsibilities, this role provides day-to-day leadership to QA Associates, including work planning, performance management, and oversight of team deliverables in partnership with the department head. Responsibilities Quality Assurance (~75%) Perform packaging line inspections/audits and ensure compliance with SOPs and GMP requirements Conduct finished product inspections and evaluate physical characteristics prior to packaging Perform in-process checks during packaging to ensure adherence to batch record specifications Review and ensure compliance of batch documentation in accordance with established procedures Monitor GMP areas to ensure compliance with 21 CFR guidelines and internal standards Perform raw material and packaging material sampling Collect stability samples, coordinate testing, and support stability programs Prepare stability protocols and assist in report compilation Perform annual retain sample inspections and manage reserve sample inventory Identify and escalate quality issues, deviations, and potential risks Team Leadership & Supervisory Responsibilities (~25%) Provide day-to-day oversight and guidance to QA Associates Assign and prioritize work based on production schedules and departmental needs in partnership with QA leadership Review team output to ensure accuracy, completeness, and compliance with GMP standards Support hiring, onboarding, and training of QA team members Approve employee time off and manage scheduling/coverage Conduct performance management activities, including mid-year and year-end reviews Coach and develop team members; provide ongoing feedback and support career development Foster a culture of accountability, teamwork, and continuous improvement Partner with cross-functional teams (Manufacturing, Packaging, QC) to resolve quality issues and improve processes Skills Strong verbal and written communication skills Leadership, coaching, and team development capabilities Ability to work in a fast-paced, dynamic environment Strong problem-solving and decision-making skills Excellent interpersonal and collaboration skills Working knowledge of GMP requirements and QA processes Requirements Bachelor’s degree required 5+ years of experience in a GMP or Quality Assurance environment (lead or senior experience preferred) Demonstrated ability to coordinate multiple tasks and priorities Ability to read, interpret, and enforce Standard Operating Procedures Strong attention to detail and organizational skills Ability to work effectively within a team environment Flexibility to support shift changes as needed The base salary range for this position is $80,000-$100,000; the exact salary depends on various factors such as experience, skills, education, location, competencies and industry-specific knowledge. ANI Pharmaceuticals offers a variety of benefits to eligible employees, including health insurance coverage, life and disability insurance, retirement savings plans, paid leave programs, paid holidays and paid time off. Many of these benefits are subsidized or fully paid for by the company. #LI-DNP

Full job record

Job IDd4040a0731f67194bbb3fb6809d19b7641b454e0
Org IDf901a054-00f8-440d-bb16-9dd44b553671
Source ID090db789-6574-433c-818a-bcb676318fb8
Board ID090db789-6574-433c-818a-bcb676318fb8
Provideroracle_hcm
Provider Job Key1405
TitleQA Team Lead
Normalized Title
Statusactive
Activeyes
Location TextEast Windsor, NJ, United States; ANI East Windsor Facility NJ, Trenton, NJ, US
Department
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionNJ
CityEast Windsor
Salary Rawsalary range for this position is $80,000-$100,000; the exact salary depends on various factors such as experience, skills, educat
Salary Min80,000
Salary Max100,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://iboijb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1003/job/1405
Apply URLhttps://iboijb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1003/job/1405
First Seen At2026-06-03 10:55:06Z
Last Seen At2026-06-06 18:59:27Z
Last Checked At2026-06-06 18:59:27Z
Last Changed At2026-06-06 11:24:23Z
Inactive At
Source Posted At2026-06-02 12:43:25Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=iboijb.fa.ocs.oraclecloud.com|CX_1003/date=2026-06-06/2026-06-06T18-59-24-003Z-c9ebeb77bf691ac7fcd9d2aa269c24d099a60d3672e7df374835fcd0dbabaef6.json
Event Fields
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Our culture empowers everyone to be successful and apply their full potential.</span></p><p><span><strong>About the Role&nbsp;</strong></span></p><p><span>This position is responsible for supporting Manufacturing and Packaging Operations to ensure compliance with applicable procedures, GMP requirements, and regulatory standards.</span></p><p><span>In addition to individual contributor responsibilities, this role provides day-to-day leadership to QA Associates, including work planning, performance management, and oversight of team deliverables in partnership with the department head.</span></p><p>&nbsp;</p><p><span><strong>Responsibilities</strong></span></p><p><span>Quality Assurance (~75%)</span></p><ul><li><span>Perform packaging line inspections/audits and ensure compliance with SOPs and GMP requirements</span></li><li><span>Conduct finished product inspections and evaluate physical characteristics prior to packaging</span></li><li><span>Perform in-process checks during packaging to ensure adherence to batch record specifications</span></li><li><span>Review and ensure compliance of batch documentation in accordance with established procedures</span></li><li><span>Monitor GMP areas to ensure compliance with 21 CFR guidelines and internal standards</span></li><li><span>Perform raw material and packaging material sampling</span></li><li><span>Collect stability samples, coordinate testing, and support stability programs</span></li><li><span>Prepare stability protocols and assist in report compilation</span></li><li><span>Perform annual retain sample inspections and manage reserve sample inventory</span></li><li><span>Identify and escalate quality issues, deviations, and potential risks</span></li></ul><p>&nbsp;</p><p><span>Team Leadership &amp; Supervisory Responsibilities (~25%)</span></p><p>&nbsp;</p><ul><li><span>Provide day-to-day oversight and guidance to QA Associates</span></li><li><span>Assign and prioritize work based on production schedules and departmental needs in partnership with QA leadership</span></li><li><span>Review team output to ensure accuracy, completeness, and compliance with GMP standards</span></li><li><span>Support hiring, onboarding, and training of QA team members</span></li><li><span>Approve employee time off and manage scheduling/coverage</span></li><li><span>Conduct performance management activities, including mid-year and year-end reviews</span></li><li><span>Coach and develop team members; provide ongoing feedback and support career development</span></li><li><span>Foster a culture of accountability, teamwork, and continuous improvement</span></li><li><span>Partner with cross-functional teams (Manufacturing, Packaging, QC) to resolve quality issues and improve processes</span></li></ul><p><span><strong>Skills</strong></span></p><ul><li><span>Strong verbal and written communication skills</span></li><li><span>Leadership, coaching, and team development capabilities</span></li><li><span>Ability to work in a fast-paced, dynamic environment</span></li><li><span>Strong problem-solving and decision-making skills</span></li><li><span>Excellent interpersonal and collaboration skills</span></li><li><span>Working knowledge of GMP requirements and QA processes</span></li></ul><p><span><strong>Requirements</strong></span></p><ul><li><span>Bachelor’s degree required</span></li><li><span>5+ years of experience in a GMP or Quality Assurance environment (lead or senior experience preferred)</span></li><li><span>Demonstrated ability to coordinate multiple tasks and priorities</span></li><li><span>Ability to read, interpret, and enforce Standard Operating Procedures</span></li><li><span>Strong attention to detail and organizational skills</span></li><li><span>Ability to work effectively within a team environment</span></li><li><span>Flexibility to support shift changes as needed</span></li></ul><p>&nbsp;</p><div style=\"color: rgb(0, 0, 0); font-family: Aptos, Aptos_EmbeddedFont, Aptos_MSFontService, Calibri, Helvetica, sans-serif; font-size: 12pt;\">The base salary range for this position is $80,000-$100,000; the exact salary depends on various factors such as experience, skills, education, location, competencies and industry-specific knowledge.</div><div style=\"color: rgb(0, 0, 0); font-family: Aptos, Aptos_EmbeddedFont, Aptos_MSFontService, Calibri, Helvetica, sans-serif; font-size: 12pt;\">&nbsp;</div><p>ANI Pharmaceuticals offers a variety of benefits to eligible employees, including health insurance coverage, life and disability insurance, retirement savings plans, paid leave programs, paid holidays and paid time off. 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