India · On-site
Required Experience of: Receipt, storage and dispensing of Raw Material & Packaging Materials as per their respective Sops. Online documentation for all transactions of materials and all activities which are to be done i…
Skills: Precision Weighing, Measuring, GMP Compliance, SOP Compliance, Documentation Accuracy
Brookhaven, New York, United States · On-site
$29/hr–$32/hr
Description: This role is responsible for ensuring the facility's electrical systems remain in optimal working condition. Duties include resetting circuit breakers, replacing lamps and ballasts, servicing light sensors a…
Skills: Electrical Troubleshooting, High-Voltage Wiring, Low-Voltage Wiring, NEC Compliance, OSHA Standards
Brookhaven, New York, United States · On-site
$28/hr–$37/hr
Description: Electricians are responsible to maintain the facility electrical system in good working condition. Including Resetting Circuit Breakers, Changing Lamps and Ballasts, Light Sensors, Switches, Changing Recepta…
Skills: Electrical Troubleshooting, Wiring Diagram Interpretation, Blueprint Reading, Control Systems Maintenance, High-Voltage Systems
Branchburg Township, New Jersey, United States · On-site
$60k–$85k/yr
Description: The QA Stability Specialist is responsible for implementing, leading and managing the iStability/LIMS software and entering the data in the software for all the ANDA batches and to perform the statistical ev…
Skills: iStability/LIMS, Statistical Evaluation, Stability Protocol Preparation, Regression Analysis, cGMP Compliance
Gujarat, India · On-site
Essential Functions: • Strong experience in solid-phase and liquid-phase peptide synthesis. • Knowledge of hybrid technologies / Molecular Hiving preferred. •Hands-on experience in process development of peptide pharmace…
Skills: Solid-phase Peptide Synthesis, Liquid-phase Peptide Synthesis, Process Development, API Production, GMP Guidelines
Piscataway Township, New Jersey, United States · On-site
$115k–$120k/yr
Senior Scientist, Quality Control: Responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedur…
Skills: Analytical Chemistry, HPLC, Dissolution Testing, cGMP, Spectrophotometry
Piscataway Township, New Jersey, United States · On-site
$75k–$90k/yr
Description: The Scientist II - QC is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written proce…
Skills: IR Spectroscopy, UV-Vis Spectroscopy, Chromatographic Techniques, X-ray Diffraction, DSC
Macon, Georgia, United States · Remote OK
$80k–$100k/yr
Description: The Sales Representative plays a crucial role in implementing marketing & sales strategies to promote our products effectively with our ENDO Sales Team. The incumbent will deliver balanced and informative sa…
Skills: Communication, Presentation Skills, Disease State Knowledge, Pharmaceutical Sales, Medical Device Sales
Piscataway, New Jersey, United States · On-site
$26/hr–$32/hr
Description: The Group Leader is responsible for leading the manufacturing process of batches. In addition, the Group Leader will perform and demonstrate the actual methods and procedures to produce the products utilizin…
Skills: Manufacturing Leadership, HMI Control Systems, cGMP Standards, Batch Record Management, Label Reconciliation
Ahmedabad, Gujarat, India · On-site
Description: This role supports the in-process quality assurance function within a pharmaceutical manufacturing environment, contributing to the definition and specification of activities, processes, and standards requir…
Skills: In-Process Quality Assurance, cGMP Compliance, Auditing, Deviation Management, Change Control
Ahmedabad, Gujarat, India · On-site
Description: This role is responsible for conducting quality testing activities on pharmaceutical products in compliance with established standards and regulatory requirements within a global pharmaceutical manufacturing…
Skills: QC Microbiology, Environmental Monitoring, Sterility Testing, Bacterial Endotoxin Test, Bioburden Testing
Kadi Taluka, Gujarat, India · On-site
Description: This role is responsible for performing a diverse range of manufacturing operations related to the processing and assembly of injectable pharmaceutical products within a regulated manufacturing environment. …
Skills: Aseptic Processing, cGMP, Injectable Manufacturing, Batch Documentation, Cleanroom Sanitization
Kadi Taluka, Gujarat, India · On-site
Description: This role is responsible for conducting environmental monitoring activities and quality analyses in compliance with established standards and regulatory requirements within a global pharmaceutical manufactur…
Skills: Environmental Monitoring, Quality Control, Pharmaceutical Manufacturing, GMP, GLP
Kadi Taluka, Gujarat, India · On-site
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated sterile manufacturing environment, with a speci…
Skills: Aseptic Technique, cGMP, Sterile Manufacturing, Equipment Operation, Batch Documentation
Kadi Taluka, Gujarat, India · On-site
Description: This role is responsible for defining and specifying the activities, processes, and standards required to fulfill quality requirements for manufactured materials, components, and products within a global pha…
Skills: Quality Assurance, GMP Guidelines, 21 CFR Part 210 & 211, Auditing, Manufacturing Process Monitoring
Hyderabad, Telangana, India · On-site
Responsible as Department training coordinator (DTC). •Responsible for training management activities. •Responsible to upload training copy of SOP in training software •Responsible to provide training log of employees in…
Skills: Quality Assurance, People Management, Compliance Audit, Talent Acquisition, Learning And Development
Hyderabad, Telangana, India · On-site
Description: Responsible for Preparation and Implementation of SOP's.Viable monitoring in clean area of manufacturing and warehouse as per the defined schedule.Responsible for personnel monitoring.Responsible to particip…
Skills: Quality Assurance, Risk Assessment, CAPA, Root Cause Analysis, cGMP
Sarkhej, Gujarat, India · On-site
Key Responsibilities Perform routine Environmental Monitoring (EM) activities in classified cleanrooms (Grade A, B, C, D areas). Conduct viable and non-viable monitoring including- Active air sampling, Surface monitoring…
Skills: Environmental Monitoring, Microbiological Testing, Sterility Testing, Aseptic Handling, GMP Compliance
Sarkhej, Gujarat, India · On-site
Key Responsibilities Lead and manage the Environmental Monitoring (EM) program for sterile injectable and peptide manufacturing areas (Grade A, B, C, D cleanrooms) including Isolator based lines. Individual should have t…
Skills: Environmental Monitoring, Microbiology, Sterile Injectable Manufacturing, Cleanroom Management, Root Cause Analysis
Sarkhej, Gujarat, India · On-site
Key Responsibilities Lead and manage the QC Chemical (Analytical) department for sterile injectable and peptide-based formulations. Oversee analysis of Raw Materials, In-Process Samples, Finished Products, Stability Samp…
Skills: QC Analytical Management, Peptide Characterization, Sterile Injectables, Analytical Method Validation, Regulatory Compliance
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Responsible for the receipt, storage, and dispensing of raw and packaging materials according to SOPs. This includes managing ERP data entry, QMS documentation, and maintaining stock records for expired or rejected materials.
Requires a D.Pharm, B.Sc, B.Pharm, or M.Sc degree with a minimum of 2 years of experience in pharma raw material handling. Candidates must be proficient in GMP compliance and warehouse documentation.
Skills :
We make healthy possible.
Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver. Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions. Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam. Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or [email protected]. If you are currently experiencing a life-threatening event, please immediately contact 911.
Offices: 400 Crossing Boulevard, Bridgewater, New Jersey 08807, US
We make healthy possible.
Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver. Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions. Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam. Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or [email protected]. If you are currently experiencing a life-threatening event, please immediately contact 911.
Offices: 400 Crossing Boulevard, Bridgewater, New Jersey 08807, US
