Piscataway Township, New Jersey, United States · On-site
$80k–$100k/yr
Description: The Supervisor will oversee the operations and staff throughout the manufacturing floor. The supervisor will also assist with equipment start-up, participate in ANDA batch production and commercial batch man…
Skills: GMP Compliance, Transdermal Drug Delivery, Staff Leadership, Equipment Validation, Production Scheduling
Ahmedabad, Gujarat, India · On-site
Description: This role is responsible for performing inspection operations within pharmaceutical manufacturing environments, ensuring that pharmaceutical products and components meet defined quality and compliance standa…
Skills: Visual Inspection, Mechanical Inspection, cGMP, Quality Assurance, Defect Identification
Ahmedabad, Gujarat, India · On-site
To operate the necessary equipment such as Vial or cartridge washing, Filling, sealing, Autoclave, Auto Visual Inspection & batch manufacturing operation. To ensure compliance with cGMP. To execute manufacturing plan as …
Skills: Vial Washing, Cartridge Filling, Sealing, Autoclave Operation, Auto Visual Inspection
Ahmedabad, Gujarat, India · On-site
Description: This role is responsible for performing a diverse range of tasks related to the processing and assembly of pharmaceutical ingredients and finished products within a regulated sterile manufacturing environmen…
Skills: Filling and Sealing, Sterile Manufacturing, cGMP, Batch Manufacturing Records, Parenteral Production
Piscataway, New Jersey, United States · On-site
$20/hr–$25/hr
Description: The Document Control Assistant is responsible for administering the processes and practices which support documentation compliance. The Specialist will work in a pharmaceutical production facility and in clo…
Skills: Document Control, cGMP, MS Word, MS Excel, MS Access
Bridgewater, New Jersey, United States · Hybrid
$120k–$145k/yr
Description: The Technical Accounting Manager will be responsible for leading key technical accounting areas, including lease accounting, complex contract accounting, accounting research, and quarterly/annual financial r…
Skills: Lease Accounting, ASC 842, U.S. GAAP, Financial Reporting, Technical Accounting Memos
Piscataway, New Jersey, United States · On-site
$75k–$95k/yr
Description: The NOI Investigations Specialist plays a critical role in ensuring product quality, compliance, and patient safety by conducting comprehensive investigations into quality events that may impact the manufact…
Skills: Root Cause Analysis, CAPA, GMP Compliance, Risk Assessment, FMEA
Brookhaven, New York, United States · On-site
$19/hr–$21/hr
Description: The Packaging Operator III is responsible for safely operating the packaging equipment to package in process products in accordance with packaging orders, while following SOPs and Maintaining 100% cGMP & com…
Skills: Packaging Equipment Operation, cGMP Compliance, SOP Adherence, Data Entry, Mechanical Skills
Ahmedabad, Gujarat, India · On-site
Key Responsibilities 1. Dossier Preparation & Submissions Prepare, review, and submit CTD / ACTD / country‑specific dossiers for: New product registrationsLine extensions (strength, pack size, shelf life)Variations and r…
Skills: Dossier Preparation, CTD/ACTD Submissions, Regulatory Strategy, Lifecycle Management, Health Authority Interaction
Ahmedabad, Gujarat, India · On-site
Description: This role is responsible for performing inspection operations within pharmaceutical manufacturing environments, ensuring that pharmaceutical products and components meet defined quality and compliance standa…
Skills: Visual Inspection, Mechanical Inspection, cGMP, Quality Assurance, Defect Identification
Ahmedabad, Gujarat, India · On-site
Description: This role is responsible for executing manufacturing and packaging operations within a regulated pharmaceutical environment, ensuring products are packed accurately, efficiently, and in compliance with cGMP …
Skills: Packaging Operations, cGMP Compliance, Batch Documentation, Equipment Qualification, Deviation Management
Gujarat, India · On-site
Essential Functions: Supervise QC laboratory operations and testing activitiesReview and interpret in-process and finished product analytical resultsEnsure compliance with GMP, GLP, and regulatory requirementsIdentify qu…
Skills: QC Laboratory Operations, GMP Compliance, GLP Compliance, Analytical Result Interpretation, CAPA
Gujarat, India · On-site
Description: The position is responsible for in-process and final product quality analyses and inspection in compliance with approved standards and regulatory requirements. The role involves interpreting and evaluating a…
Skills: Quality Control, Analytical Testing, GMP Compliance, GLP, Method Validation
India · On-site
Description: This role is responsible for performing a variety of tasks related to the compression and coating of pharmaceutical tablets within a regulated manufacturing environment. The incumbent operates tablet compres…
Skills: Tablet Compression, Tablet Coating, cGMP, FDA Guidelines, EMA Guidelines
India · On-site
Job description: Operate and monitor granulation equipment and related manufacturing apparatus in accordance with validated procedures and GMP standards. Supervision of Mfg activities (Equipment like RMG,FBE,FBD,RMG 800)…
Skills: Granulation, Blending, GMP Standards, Equipment Validation, PQ Execution
India · On-site
Description: This role supports manufacturing operations for oral solid dosage (OSD) products by executing routine production activities in a regulated pharmaceutical environment. The role involves operating equipment us…
Skills: Granulation, Blending, Compression, Coating, cGMP Compliance
Ahmedabad, Gujarat, India · On-site
Description: Responsible for implementing and supporting environmental, health, and safety (EH&S) programs to ensure compliance with regulatory requirements, workplace safety standards, and environmental protection polic…
Skills: EH&S Implementation, Hazard Identification, Risk Assessment, Safety Auditing, Incident Investigation
Visakhapatnam, Andhra Pradesh, India · On-site
Description: Responsible for implementing and maintaining Process Safety Management (PSM) systems to ensure safe plant operations. Conducts hazard identification studies, risk assessments, HAZOP reviews, incident investi…
Skills: Process Safety Management, Hazard Identification, Risk Assessment, HAZOP, Incident Investigation
Ahmedabad, Gujarat, India · On-site
Plan, coordinate and execute mechanical engineering activities for projects (greenfield/brownfield) Review BOQs, layouts, specifications and ensure installation of HVAC, utilities and cleanroom systems as per cGMP & FDA …
Skills: Mechanical Engineering, HVAC Systems, Cleanroom Design, Project Management, Vendor Management
Ahmedabad, Gujarat, India · On-site
Key Responsibilities: 1. CSV Strategy & Governance - Develop and maintain the overall CSV strategy and validation master plans for global systems. - Ensure compliance with GAMP 5, USFDA, EU Annex 11, 21 CFR Part 11, and …
Skills: Computer System Validation, GAMP 5, 21 CFR Part 11, EU Annex 11, GxP Compliance
Piscataway Township, New Jersey, United States • On-site
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Oversee night shift manufacturing operations to ensure safety, quality, and 100% GMP compliance. Act as a working supervisor by performing manufacturing processes, training staff, and supporting R&D scale-up activities.
Requires an Associate degree (Bachelor's preferred) and at least 3 years of experience in GMP manufacturing and staff leadership. Specialized knowledge in transdermal drug delivery, converting, and packaging is required.
The Supervisor will oversee the operations and staff throughout the manufacturing floor. The supervisor will also assist with equipment start-up, participate in ANDA batch production and commercial batch manufacturing.
Essential Functions:
Actively perfrom and demonstrate manufacturing processes while supervising daily operations
Conduct mixing, coating, converting, pouching and cartoning operations.
Additional Responsibilities:
Perform Continuous Improvements.
Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at [email protected]. Requests will be handled confidentially and in accordance with applicable laws.
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
