Home › Companies › Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003 › SUPERVISOR, QUALITY CONTROL LAB
SUPERVISOR, QUALITY CONTROL LAB
Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003 · Irvine, CA, US, Irvine, CA · Active · $80,000–$100,000 / year · ADP Workforce Now Recruiting
Job facts
| Field | Value |
|---|---|
| Company | Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003 |
| Title | SUPERVISOR, QUALITY CONTROL LAB |
| Normalized title | - |
| Department / team | - |
| Location | Irvine, CA, United States |
| Work model | - |
| Employment type | Full Time |
| Salary | $80,000–$100,000 / year |
| Status | active |
| ATS provider | ADP Workforce Now Recruiting |
| Posted / first seen | 2026-04-16 / 2026-05-31 |
| Changed / last seen | 2026-06-06 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through ADP Workforce Now Recruiting. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in Irvine. | 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 | Fbb6193d 556c 4b29 98e5 7306aa3f6384 19000101 000003 |
| Source | e088055a-0c65-47db-aa4c-74f9b0047486 |
| ATS provider | ADP Workforce Now Recruiting |
Description
RESPONSIBILITIES:
Supervises the daily activities of the QC laboratory by establishing testing priorities and schedules and assignments of staff. Provides daily direction, guidance and feedback to employees based on work priorities and schedules. Assures appropriate review of analytical results commensurate within the company review policy. Conducts employee performance review, compensation reviews and new employee recruitment. Supervises and performs laboratory investigations. Maintains equipment calibration schedule and ensures that all required calibrations and maintenance are completed in a timely fashion. Authors standard operating procedures and assist with revision process of current procedures. Ensures laboratory compliance with applicable regulations. Performs and/or assists with procedural, cGMP, and safety training of laboratory staff. Acts as communication liaison for laboratory with other facility departments. Serve as backup for laboratory Management. May performs analytical testing of raw materials, in-process samples, and finished products using analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus as necessary. Assists with preparations for internal and external laboratory audits and inspections. Other related duties as required.
REQUIRED QUALIFICATIONS:
Bachelor’s or higher degree in Chemistry or related discipline, or equivalent combination of education and experience. 8 + years’ experience in a GMP analytical chemistry laboratory, including analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus. Demonstrated ability to act in a Lead capacity and provide direction to others. Ability to build relationships at all levels of the organization. Strong communication and demonstrated listening skills. Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision. Strong attention to detail.
At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.
Full job record
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| Org ID | 1c12f03c-6518-4018-9e8a-db5c3c140f34 |
| Source ID | e088055a-0c65-47db-aa4c-74f9b0047486 |
| Board ID | e088055a-0c65-47db-aa4c-74f9b0047486 |
| Provider | adp_workforcenow |
| Provider Job Key | 514447 |
| Title | SUPERVISOR, QUALITY CONTROL LAB |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | Irvine, CA, US, Irvine, CA |
| Department | — |
| Team | — |
| Employment Type | full_time |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | CA |
| City | Irvine |
| Salary Raw | 80000.00 To 100000.00 (USD) Annually |
| Salary Min | 80,000 |
| Salary Max | 100,000 |
| Salary Currency | USD |
| Salary Period | year |
| Source URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=fbb6193d-556c-4b29-98e5-7306aa3f6384&ccId=19000101_000003&lang=en_US&type=JS&jobId=514447&jwId=9200821628099_1 |
| Apply URL | https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=fbb6193d-556c-4b29-98e5-7306aa3f6384&ccId=19000101_000003&lang=en_US&type=JS&jobId=514447&jwId=9200821628099_1 |
| First Seen At | 2026-05-31 18:58:01Z |
| Last Seen At | 2026-06-06 12:58:45Z |
| Last Checked At | 2026-06-06 12:58:45Z |
| Last Changed At | 2026-06-06 12:58:45Z |
| Inactive At | — |
| Source Posted At | 2026-04-16 16:54:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=adp_workforcenow/board=fbb6193d-556c-4b29-98e5-7306aa3f6384|19000101_000003/date=2026-06-06/2026-06-06T12-58-44-922Z-ddd9671f0b308db51448c9dbd528c5c83a531bc0232614a44d7aa5a0b50736e4.json |
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"requisitionDescription": "<div><div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;' data-pasted=\"true\"><strong><span style=\"font-size:15px;\">RESPONSIBILITIES:</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong> </strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Supervises the daily activities of the QC laboratory by establishing testing priorities and schedules and assignments of staff. </span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Provides daily direction, guidance and feedback to employees based on work priorities and schedules.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Assures appropriate review of analytical results commensurate within the company review policy. </span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Conducts employee performance review, compensation reviews and new employee recruitment. </span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Supervises and performs laboratory investigations.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Maintains equipment calibration schedule and ensures that all required calibrations and maintenance are completed in a timely fashion.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Authors standard operating procedures and assist with revision process of current procedures.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Ensures 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ICP, FTIR, TOC and dissolution apparatus as necessary.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Assists with preparations for internal and external laboratory audits and inspections.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Other related duties as required.</span></li></ul></div><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong> </strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong><span style=\"font-size:15px;\"> </span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong><span style=\"font-size:15px;\">REQUIRED QUALIFICATIONS:</span></strong></p><p style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><strong><span style=\"font-size:15px;\"> </span></strong></p><div style='margin:0in;font-size:16px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left: 0in;\"><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Bachelor’s or higher degree in Chemistry or related discipline, or equivalent combination of education and experience.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">8 + years’ experience in a GMP analytical chemistry laboratory, including analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC and dissolution apparatus.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Demonstrated ability to act in a Lead capacity and provide direction to others.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Ability to build relationships at all levels of the organization.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Strong communication and demonstrated listening skills.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision.</span></li><li style=\"margin:0in;font-size:16px;font-family: initial;\"><span style=\"font-size:15px;\">Strong attention to detail. </span></li></ul><p><br></p><p><span style=\"font-size:15px;\"><span style=\"color: rgb(36, 36, 36); font-family: Aptos, sans-serif; font-size: 14.6667px; font-style: normal; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial; display: inline !important; float: none;\" data-pasted=\"true\">At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.</span></span></p><p><br></p><p><span style=\"font-size:15px;\"><br></span></p></div></div></div>\n",
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