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Full-time
bachelor degree, postgraduate degree, professional certificate
Posted 29d ago
Apply by Sep 29
~40 hrs/week
Responsibilities
Perform visual and mechanical inspections of pharmaceutical products and packaging to ensure compliance with quality standards and cGMP. Identify and segregate non-conforming materials while maintaining accurate documentation and supporting continuous improvement efforts.
Requirements
Requires a Bachelor's degree in Science (B.Sc.), with a Master's degree preferred. Candidates should have 2 to 7 years of experience in pharmaceutical inspection or manufacturing.
Full job description
Description:
This role is responsible for performing inspection operations within pharmaceutical manufacturing environments, ensuring that pharmaceutical products and components meet defined quality and compliance standards in accordance with current Good Manufacturing Practices (cGMP). The incumbent conducts visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects, non-conformances, and deviations from established specifications. This position adheres to standard operating procedures and quality standards to maintain product integrity, safety, and compliance throughout the inspection process. The role supports the overall quality assurance function by identifying and segregating non-conforming products and reporting inspection findings accurately and in a timely manner. It contributes to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols. The position participates in training programs to develop technical competencies in inspection techniques, regulatory requirements, and quality standards applicable to pharmaceutical manufacturing. It supports continuous improvement efforts by identifying and reporting deviations and contributing to corrective and preventive action processes.
Essential Functions:
Perform visual and mechanical inspection of pharmaceutical products, packaging materials, and components to identify defects and non-conformances.
Adhere to current Good Manufacturing Practices (cGMP) and standard operating procedures during all inspection activities.
Identify, segregate, and report non-conforming products and materials in accordance with established quality procedures.
Maintain accurate and complete inspection records and documentation as required by regulatory standards.
Contribute to maintaining a clean, organized, and compliant work area in accordance with area cleaning and sanitization protocols.
Operate inspection equipment and tools in accordance with established procedures and safety guidelines.
Participate in training programs to develop technical competencies in inspection techniques and quality standards.
Support continuous improvement efforts by identifying and reporting deviations and contributing to CAPA processes.
Comply with all regulatory requirements and internal policies applicable to pharmaceutical manufacturing and inspection operations.
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
How many Science & Research jobs are open in Ahmedabad, India right now?
There are currently 105 open science & research positions in Ahmedabad, India listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Ahmedabad, India?
Companies currently hiring include Amneal Pharmaceuticals, Baxter International Inc., Agilent Technologies, Anton Paar, Cadila Pharmaceuticals Limited, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Ahmedabad, India?
Yes — 6 of the 105 open science & research positions offer remote or hybrid work (5 remote, 1 hybrid).
How do I apply for Science & Research jobs in Ahmedabad, India?
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