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This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues …
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Full-time
bachelor degree, postgraduate degree
Posted 2h ago
Apply by Aug 30
~40 hrs/week
Responsibilities
This role defines and maintains quality standards and infrastructure for laboratory operations within a global pharmaceutical environment. It involves conducting audits, managing vendor quality, and troubleshooting manufacturing process deviations to ensure regulatory compliance.
Requirements
The position requires a Bachelor of Pharmacy degree, with a Master of Pharmacy preferred. Candidates must possess 5 to 8 years of relevant experience in laboratory quality assurance and pharmaceutical manufacturing.
Full job description
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 pharmaceutical environment. The position builds and maintains the infrastructure and systems necessary to consistently ensure the timely delivery of quality-compliant products. It supports the auditing, monitoring, and evaluation of laboratory quality activities against defined internal and regulatory standards. The role ensures efficient and effective workflows, procedures, policies, and laboratory inspection programs are in place and adhered to across quality laboratory operations. It manages in-process product quality in coordination with vendors and contract manufacturers. The position facilitates communication with customers and vendors to resolve quality-related issues in a timely and compliant manner. It reports and troubleshoots manufacturing process deviations and defects identified in finished goods. The role contributes to continuous improvement initiatives aimed at reducing defects, errors, and rework across laboratory and manufacturing operations. It also supports the identification and development of outsourcing vendors and suppliers according to organizational quality standards.
Essential Functions:
Define and specify quality activities, processes, and standards for laboratory quality assurance programs in compliance with regulatory requirements
Build and maintain quality infrastructure and systems to ensure timely delivery of compliant pharmaceutical products
Conduct audits and monitoring of laboratory quality activities and outputs against internal and regulatory standards including 21 CFR Part 210 & 211 and GMP guidelines
Ensure efficient workflow, procedures, policies, and laboratory inspection programs are implemented and maintained across quality laboratory operations
Manage in-process product quality in coordination with vendors and contract manufacturers to meet defined quality specifications
Communicate with customers and vendors to investigate and resolve quality and laboratory-related issues in a timely manner
Report and troubleshoot manufacturing process deviations and defects identified in laboratory testing and finished goods
Identify and implement process improvements to reduce costs, defects, errors, and rework in laboratory and manufacturing operations
Support the identification and development of outsourcing vendors and suppliers according to organizational quality standards and policies
Additional Responsibilities:
Related keywords
Quality AssuranceLaboratoryPharmaceuticalGMP21 CFR Part 21021 CFR Part 211ComplianceAuditingManufacturingVendor ManagementProcess ImprovementQuality ControlRegulatory StandardsLaboratory InspectionDeviation ManagementFinished Goods
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.
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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?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.