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Jobs at LGM Pharma (Now Hiring) — 9 open

LGM Pharma logoLGM Pharma

PRODUCTION CONTROL COORD

Rosenberg, Texas, United States · On-site

$25/hr–$28/hr

Senior

RESPONSIBILITIES: Request Batch Records according to lots scheduled for production via the Batch Record tracker. Support manufacturing on the workflow of batch records between Manufacturing, IPQA, and QA, and other depar…

Skills: Batch Record Management, Good Documentation Practices, SAP ERP, Inventory Control, Production Planning

LGM Pharma logoLGM Pharma

SENIOR QA SPECIALIST - VALIDATION

Irvine, California, United States · On-site

$75k–$90k/yr

Senior

RESPONSIBILITIES: Assists in assuring facility, manufacturing, packaging, and Laboratory equipment are qualified to the required cGMP standards.Authors/approves and executes qualification protocols and reports.Schedules,…

Skills: Equipment Qualification, cGMP Standards, Validation Master Plan, Protocol Authoring, Vendor Qualification

LGM Pharma logoLGM Pharma

MANUFACTURING ENGINEER

Rosenberg, Texas, United States · On-site

$80k–$100k/yr

Senior

Manufacturing & Equipment Support Provide technical leadership in Troubleshooting manufacturing and packaging equipment to minimize downtime and improve equipment reliability.Analyze manufacturing performance data to inc…

Skills: Troubleshooting, Root Cause Analysis, Equipment Qualification, Process Validation, Lean Manufacturing

LGM Pharma logoLGM Pharma

ATS CHEMIST III

Irvine, California, United States · On-site

$34/hr–$38/hr

Senior

PRIMARY DUTIES AND RESPONSIBILITIES: Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products.Utilize analytical laboratory instrumentation with supervision.Comply with cG…

Skills: Analytical Testing, cGMP Regulations, Method Validation, Method Troubleshooting, HPLC

LGM Pharma logoLGM Pharma

QC CHEMIST II

Irvine, California, United States · On-site

$30/hr–$34/hr

Mid level

RESPONSIBILITIES: • Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products. • Utilize analytical laboratory instrumentation with minimal supervision. • Co…

Skills: Analytical Testing, cGMP Regulations, Peer Review, Equipment Calibration, HPLC

LGM Pharma logoLGM Pharma

QC CHEMIST III

Irvine, California, United States · On-site

$34/hr–$38/hr

Senior

We have an open QC CHEMIST III position in our Quality Control Department in the Irvine, CA location. PRIMARY DUTIES AND RESPONSIBILITIES: Perform and/or assist with analytical testing of raw materials, in-process sample…

Skills: Analytical Testing, Instrumentation Troubleshooting, Laboratory Investigations, Peer Review, Method Validation

LGM Pharma logoLGM Pharma

R&D TECHNICIAN

Rosenberg, Texas, United States · On-site

$22/hr–$25/hr

Entry level

RESPONSIBILITIES: Conduct hand, laboratory, and pilot scale, new and reformulation product trials, and write reports. Support Scientists in conducting product development trials and pilot batches by gathering raw materia…

Skills: Product Development, Laboratory Techniques, Pilot Scale Batching, CGMP, Physical Testing

LGM Pharma logoLGM Pharma

ASSOCIATE SALES REPRESENTATIVE

Boca Raton, Florida, United States · On-site

$56k–$65k/yr

Mid level

We have an open position for an Associate Sales Representative for the LGM - Willow Birch Pharma based in the Boca Raton, FL location. The ideal candidate is energetic, competitive, and self-driven, with a passion for bu…

Skills: Cold Calling, Prospecting, Business Development, Account Management, Salesforce CRM

LGM Pharma logoLGM Pharma

SUPERVISOR, QUALITY ASSURANCE

Erlanger, Kentucky, United States · On-site

$73k–$90k/yr

Senior

Position Summary The Supervisor, Quality Assurance role is responsible for day-to-day quality oversight of warehouse and distribution operations at an FDA-registered API distribution facility. This role ensures that all …

Skills: Quality Assurance, GMP Compliance, GDP Principles, Root Cause Analysis, CAPA

LGM Pharma logo

PRODUCTION CONTROL COORD

LGM Pharma

Rosenberg, Texas, United States • On-site

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Senior

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  • $25/hr–$28/hr
  • Full-time
  • high school
  • Medical, Dental, Vision, 401k Matching
  • Posted 6d ago
  • ~40 hrs/week

Responsibilities

Coordinate the workflow and review of batch records to ensure compliance with Good Documentation Practices and timely closure. Support production planning by monitoring floor progress, managing inventory transactions in SAP, and generating operational reports.

Requirements

Requires a High School Diploma or GED with a preference for 5+ years of experience in Oral Solid Dose manufacturing. Proficiency in Microsoft Office (specifically Pivot Tables and VLOOKUP) and experience with SAP ERP are highly desired.

Full job description

RESPONSIBILITIES:

  • Request Batch Records according to lots scheduled for production via the Batch Record tracker. 
  • Support manufacturing on the workflow of batch records between Manufacturing, IPQA, and QA, and other departments to ensure timely movement and closure of documentation. 
  • Review batch records for Good Documentation Practices (GDP), ensure completeness, calculation accuracy, and free of documentation errors/omissions.
  • Assist Manufacturing personnel in correcting GDP errors and documentation discrepancies in accordance with company procedures.
  • Assist production planning activities by monitoring the progress on the floor and communicating any issues. 
  • Support Manufacturing in verifying material consumption, issuance, and inventory transactions by comparing SAP/ERP records against batch documentation. 
  • Assist with reconciliation activities related to inventory cards, batch documentation, and material usage records. 
  • Generate and maintain production-related reports including labor utilization, production metrics, SAP transaction reports, KPI tracking, and operational summaries.
  • Coordinate office and production supply requests and maintain inventory of operational consumables through Kanban or other inventory control systems. 
  • Assist with the development of OJT (On the Job Training) and provide support with SOP updates and revisions.
  • Assist with tracking of tooling, utensils, production supplies, and operational materials. 
  • Participate in inventory counts, reconciliation activities, and operational audits as required.
  • Support proper disposition and coordination of rejected or obsolete materials in collaboration with QA and Warehouse departments. 
  • Perform additional production support activities as assigned by Production Management.

 

QUALIFICATIONS:

 

  • High School Diploma or General Education Degree (GED) and/or equivalent experience. 
  • 5+ years of manufacturing experience preferred in Oral Solid Dose Manufacturing (Tablets and Capsules) with combination floor and production control experience.
  • Strong proficiency with Microsoft Office applications such as Word, PowerPoint and Excel functions such as Pivot Tables, VLOOKUP, filters, and data tracking are preferred. 
  • Experience with SAP ERP system desire.
  • Ability to manage multiple priorities in a fast-paced manufacturing environment.
  • Excellent communication skills both written and verbal.
  • Great organizational skills and attention to detail, desire 
  • Bi-lingual (Spanish and English) desire

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.

Related keywords

Batch RecordsGDPSAPERPOral Solid DoseTabletsCapsulesKanbanKPIOJTSOPInventory ManagementProduction ControlMaterial ConsumptionLabor Utilization

About LGM Pharma

LinkedInVisit site

We Accelerate and Optimize the New Product Pathway from Early Development Through Commercialization.

Industry
Pharmaceutical Manufacturing
Company size
51-200 employees
Founded
2005
Headquarters
Boca Raton, Florida
LinkedIn followers
5,445

LGM Pharma is a leading CDMO provider of comprehensive API sourcing and drug product contract development and manufacturing solutions to the pharmaceutical industry. We secure and optimize your supply chain with our extensive qualified API partner network, global drug product development and manufacturing facilities, and regulatory and market intelligence services delivering customized solutions that get your products to market faster. Full-service, expert support that accelerates the new product pathway. Now that’s smart. • Established in 2005 • ISO 9001-2015 QMS certified company • CGMP systems in accordance with ICH Q7 • Main business segments: R&D / Biotech / CDMO / Specialty Pharma Companies, New Drug Delivery Technologies (NDA/505b2) – with heavy concentration on injectables, transdermal, nasal, inhalation, ophthalmic & sublingual drug deliveries Our products originate from our API manufacturing partner sites who are approved by the leading regulatory authorities, such as the US-FDA, EDQM, TGA, UK-MHRA, PMDA etc. LGM’s industry experience enables us to support our clients throughout the entire pathway of drug development, from discovery through commercial production. Based on the scale and scope of development projects with which we are involved, we are able to provide our customers with a seasoned perspective and valuable market insight. LGM Pharma has enhanced its position as a leading supplier of newly approved APIs, including full technical documentation and regulatory support. Our Clients: At LGM Pharma, our clients’ needs are our top priority, and we support our client base consisting of a diverse array of pharma companies, including: • Contract Research, Development & Manufacturing Organizations • Specialty Pharma and Novel Drug Delivery Systems • R&D & Biotech Companies • Generic Pharma Companies • Chemical Catalog Companies • OTC & Private Label Manufacturers • Academic & Government Laboratories • Pharmacy Compounding Industry

Offices: 6400 Congress Ave, Suite 1400, Boca Raton, Florida 33487, US · 2758 Circleport Dr, Erlanger, Kentucky 41018, US · Hamelacha St. 15, Industrial Park Har Tuv A, Beit Shemesh, 9905515, IL · 1815 E Cheyenne Rd, Colorado Springs, Colorado 80905, US · 17802 Gillette Ave, Irvine, California 92614, US

CDMOAPI SourcingSupply Chain ManagementDrug ManufacturingDrug DevelopmentRegulatory Submissionand 505(b)(2)Pharmaceutical
View all jobs at LGM Pharma

About LGM Pharma

LinkedInVisit site

We Accelerate and Optimize the New Product Pathway from Early Development Through Commercialization.

Industry
Pharmaceutical Manufacturing
Company size
51-200 employees
Founded
2005
Headquarters
Boca Raton, Florida
LinkedIn followers
5,445

LGM Pharma is a leading CDMO provider of comprehensive API sourcing and drug product contract development and manufacturing solutions to the pharmaceutical industry. We secure and optimize your supply chain with our extensive qualified API partner network, global drug product development and manufacturing facilities, and regulatory and market intelligence services delivering customized solutions that get your products to market faster. Full-service, expert support that accelerates the new product pathway. Now that’s smart. • Established in 2005 • ISO 9001-2015 QMS certified company • CGMP systems in accordance with ICH Q7 • Main business segments: R&D / Biotech / CDMO / Specialty Pharma Companies, New Drug Delivery Technologies (NDA/505b2) – with heavy concentration on injectables, transdermal, nasal, inhalation, ophthalmic & sublingual drug deliveries Our products originate from our API manufacturing partner sites who are approved by the leading regulatory authorities, such as the US-FDA, EDQM, TGA, UK-MHRA, PMDA etc. LGM’s industry experience enables us to support our clients throughout the entire pathway of drug development, from discovery through commercial production. Based on the scale and scope of development projects with which we are involved, we are able to provide our customers with a seasoned perspective and valuable market insight. LGM Pharma has enhanced its position as a leading supplier of newly approved APIs, including full technical documentation and regulatory support. Our Clients: At LGM Pharma, our clients’ needs are our top priority, and we support our client base consisting of a diverse array of pharma companies, including: • Contract Research, Development & Manufacturing Organizations • Specialty Pharma and Novel Drug Delivery Systems • R&D & Biotech Companies • Generic Pharma Companies • Chemical Catalog Companies • OTC & Private Label Manufacturers • Academic & Government Laboratories • Pharmacy Compounding Industry

Offices: 6400 Congress Ave, Suite 1400, Boca Raton, Florida 33487, US · 2758 Circleport Dr, Erlanger, Kentucky 41018, US · Hamelacha St. 15, Industrial Park Har Tuv A, Beit Shemesh, 9905515, IL · 1815 E Cheyenne Rd, Colorado Springs, Colorado 80905, US · 17802 Gillette Ave, Irvine, California 92614, US

CDMOAPI SourcingSupply Chain ManagementDrug ManufacturingDrug DevelopmentRegulatory Submissionand 505(b)(2)Pharmaceutical
View all jobs at LGM Pharma

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