Ankleshwar, Gujarat, India · On-site
Role Objective / Major Purpose of the Job - Apprentice The Quality Assurance (QA) Apprentice is responsible for supporting quality assurance activities to ensure products are manufactured in compliance with cGMP, SOPs, r…
Skills: Quality Assurance, Cgmp, Gdp, Batch Manufacturing Record, Documentation Review
Ankleshwar, Gujarat, India · On-site
Manage and supervise complete shift production activities for API manufacturing. Execute manufacturing batches as per approved BMR, SOPs and process parameters. Monitor critical process parameters such as temperature, pr…
Skills: API manufacturing, Shift management, Batch process execution, BMR documentation, GMP compliance
Ankleshwar, Gujarat, India · On-site
Production : • To receive crude solvents from plants and issue recovered solvents to plants. • To check the labels of raw material, packing materials and solvents before usage. • Perform column distillation as per SDR. •…
Skills: Solvent distillation, Batch processing, cGMP compliance, Chemical handling, Equipment maintenance
Ankleshwar, Gujarat, India · On-site
Job Purpose To perform and document analytical testing of raw materials, intermediates, APIs, in-process and finished products in accordance with approved specifications, analytical methods, SOPs, GMP and data-integrity …
Skills: HPLC, GC, Analytical Testing, Quality Control, GMP
Ankleshwar, Gujarat, India · On-site
Execute day-to-day API manufacturing operations as per approved BMR, SOPs and production plans. Supervise and monitor manufacturing processes including charging, reaction, heating/cooling, distillation, extraction, cryst…
Skills: API Manufacturing, GMP Compliance, SOP Adherence, Process Monitoring, Batch Record Review
Ankleshwar, Gujarat, India · On-site
Manage and supervise complete shift production activities for API manufacturing. Execute manufacturing batches as per approved BMR, SOPs and process parameters. Monitor critical process parameters such as temperature, pr…
Skills: API Manufacturing, Shift Management, Batch Process Execution, BMR Documentation, GMP Compliance
Ankleshwar, Gujarat, India · On-site
Execute day-to-day API manufacturing operations as per approved BMR, SOPs and production plans. Supervise and monitor manufacturing processes including charging, reaction, heating/cooling, distillation, extraction, cryst…
Skills: API Manufacturing, BMR Documentation, SOP Compliance, GMP Standards, Process Monitoring
Ankleshwar, Gujarat, India · On-site
Perform and review analysis of raw materials, intermediates, finished products, in-process, stability, water, and cleaning validation samples as per approved specifications and test methods. Operate, troubleshoot, and ma…
Skills: HPLC, GC, UV-Visible Spectrophotometry, FTIR, Karl Fischer Titration
Ankleshwar, Gujarat, India · On-site
Execute API manufacturing activities as per Batch Manufacturing Records (BMR) and approved Standard Operating Procedures (SOPs). Operate and monitor reactors, centrifuges, dryers, filters, blenders, micronizers, and othe…
Skills: API Manufacturing, cGMP, GDP, Data Integrity, Equipment Operation
Ankleshwar, Gujarat, India · On-site
Documentation: • To prepare SOP’s/ URS/ BPR/ Protocol/ Investigation report for regulatory compliance as per available procedure/practice. • Ensure that all documents / records required for Regulatory Compliance are main…
Skills: SOP Preparation, Regulatory Compliance, GDP, GMP Compliance, CAPA
Ankleshwar, Gujarat, India · On-site
Production Management Plan, coordinate, and supervise daily API manufacturing activities in line with the approved production plan. Ensure timely execution and completion of batches as per BMR/BPR, SOPs, process paramete…
Skills: API Manufacturing, Chemical Synthesis, GMP Compliance, Team Leadership, Process Optimization
Ankleshwar, Gujarat, India · On-site
• To ensure cGMP compliance at manufacturing facility [PR, PR (SRP), Quality units, HR, EHS, ST, EG departments] as well as to ensure the whether they are following the standard procedures. • Responsible to ensure online…
Skills: cGMP Compliance, Data Integrity, Line Clearance, Quality Assurance, CAPA
Ankleshwar, Gujarat, India · On-site
Review and approve batch manufacturing records (BMR), batch packaging records (BPR), logbooks, and analytical reports. Perform line clearance activities before and after manufacturing operations. Monitor and verify compl…
Skills: cGMP, GDP, Data Integrity, SOP Review, Line Clearance
Ankleshwar, Gujarat, India · On-site
Execute API manufacturing processes as per approved BMR, SOPs, process parameters, and production schedules. Supervise day-to-day production activities including charging, reaction, heating/cooling, distillation, extract…
Skills: API manufacturing, GMP compliance, Process parameter monitoring, BMR documentation, Chemical synthesis
Ankleshwar, Gujarat, India · On-site
• Work allocation for sampling , analysis related to microbial testing based on requirement and plan for sampling and analysis of finish products, & (test procedures and SOPs, and review of analysis data generated throug…
Skills: Microbial testing, LIMS, SAP, Calibration, Instrument maintenance
Ankleshwar, Gujarat, India · On-site
Process Development: • Conduct laboratory experiments & trials to modify processes develop shorter processes to reduce present cost. • Send sample to QC of studied experiment. • Contact QC dept. to solicit support & foll…
Skills: Process Development, Laboratory Experiments, Sample Analysis, Data Generation, Vendor Qualification
Ankleshwar, Gujarat, India · On-site
Participate in customer, regulatory, and internal audits including USFDA, MHRA, WHO-GMP, EDQM, and other global regulatory inspections. Provide analytical data and laboratory documentation during inspections. Ensure audi…
Skills: Regulatory Audits, Analytical Documentation, cGMP, GLP, Data Integrity
Ankleshwar, Gujarat, India · On-site
Ensure compliance with cGMP, GDP, GLP, Data Integrity (ALCOA+), SOPs, and regulatory guidelines. Perform shop floor QA activities, including line clearance, equipment clearance, area clearance, and in-process verificatio…
Skills: cGMP, GDP, GLP, Data Integrity, Line Clearance
Ankleshwar, Gujarat, India · On-site
Execute API manufacturing activities as per approved BMR, SOPs, and production plans. Supervise shift operations involving reactors, centrifuges, dryers, filters, and other process equipment. Ensure compliance with cGMP,…
Skills: API Manufacturing, cGMP, GDP, EHS, Data Integrity
Ankleshwar, Gujarat, India · On-site
Production Management Plan, coordinate, and supervise daily API manufacturing activities in line with the approved production plan. Ensure timely execution and completion of batches as per BMR/BPR, SOPs, process paramete…
Skills: API manufacturing, Chemical synthesis, GMP, Team management, Process optimization
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The Quality Assurance Apprentice supports quality assurance activities to ensure manufacturing compliance with cGMP, SOPs, and regulatory standards. Responsibilities include reviewing production documentation, performing shop-floor inspections, and assisting in investigations and internal audits.
The candidate should have basic knowledge of Quality Assurance principles, cGMP, and GDP documentation practices. Strong attention to detail, teamwork, and communication skills are essential for this role.
Role Objective / Major Purpose of the Job - Apprentice
The Quality Assurance (QA) Apprentice is responsible for supporting quality assurance activities to ensure products are
manufactured in compliance with cGMP, SOPs, regulatory requirements, and company quality standards. The role assists in
documentation, inspections, audits, and quality systems while ensuring product quality, data integrity, and continuous
improvement.
Principal Tasks & Responsibilities
-Assist in implementing and maintaining Quality Assurance systems in accordance with cGMP, GDP, and regulatory requirements.
-Review Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and other production documents for
completeness and accuracy.
- Perform line clearance verification before and after manufacturing and packaging activities.
- Support in-document review, issuance, retrieval, and archival of controlled documents.
- Assist in monitoring Good Documentation Practices (GDP) across manufacturing areas.
- Participate in in-process quality checks and routine shop-floor inspections.
- Report deviations, non-conformances, and quality incidents to the QA Officer or Supervisor.
- Assist in investigations, CAPA implementation, change control, and risk assessment activities.
- Support internal audits, self-inspections, customer audits, and regulatory inspections.
- Ensure calibration, qualification, and validation documents are maintained as per SOPs.
- Coordinate with Production, QC, and Warehouse, Engineering, and EHS departments to ensure compliance.
- Maintain accurate records in logbooks, quality systems, and electronic databases where applicable.
- Support training activities related to GMP, SOPs, and quality systems.
- Follow safety procedures and ensure compliance with EHS requirements.
Key Skills & Competencies
Functional / Technical:
- Basic knowledge of Quality Assurance principles
- cGMP, GDP, and regulatory compliance
- Batch Manufacturing Record (BMR) and documentation review
- Good Documentation Practices (GDP)
- Deviation, CAPA, and Change Control awareness
- Internal audit and inspection support
- Validation and qualification basics
- Data integrity principles
Behavioural:
- Attention to Detail
- Teamwork and Collaboration
- Strong Communication Skills
- Problem-Solving Ability
- Learning Agility
The Care Continues...
Founded by Shri I.A. Modi, Cadila Pharmaceuticals Ltd. is one of the largest privately held pharmaceutical companies in India, headquartered at Ahmedabad, in the State of Gujarat. Over the last seven decades, the company has been developing and manufacturing pharmaceutical products in India and selling and distributing these in over hundred other countries around the world. Focused strongly on Innovation and Research, the company is present in more than forty-five therapeutic areas spread across twelve specialities, including cardiovascular, gastrointestinal, analgesics, haematinics, anti-infectives and antibiotics, respiratory agents, antidiabetics and immunologicals. At Cadila Pharmaceuticals, Research and Development is at the core of all its initiatives, be it Biotechnology, APIs, Formulations, Plant Tissue Culture or Phytochemistry. More than 300 scientists in its various Research and Development setups reinforce the competitiveness of research in the therapeutic areas which have high unmet medical needs. Cadila Pharmaceuticals Excellence in manufacturing facilities is central to Cadila Pharmaceuticals. The company’s formulations manufacturing plant at Dholka near Ahmedabad, Gujarat is spread over hundred acres of land. This state-of-the- art facility is not only impressive in size, but is also USFDA approved. The second formulations manufacturing facility is located at Samba in Jammu and Kashmir. The facility meets most of the stringent quality standards across the globe to produce tablets, capsules, soft and hard gelatin capsules, liquids and orals. Two Active Pharmaceutical Ingredient (API) manufacturing units at Ankleshwar, Gujarat manufacture a wide range of APIs and intermediates including many USFDA-certified products. The company has strong foothold in the African continent through its formulation manufacturing facility at Addis Ababa in Ethiopia. For more information visit: https://www.cadilapharma.com/
Offices: Sarkhej-Dholka Road, Bhat, Ahmedabad, Gujarat 382210, IN · Survey No. 1389, Trasad Road, Dholka, Ahmedabad, Gujarat 387 810, IN · 294, GIDC Estate, Ankleshwar, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN · Survey No. 342, Nani Kadi, Taluka Kadi, Dist. Mehsana, Gujarat, IN
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