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0-2 years
Not Disclosed
Digwal, Telangana, India
10 June 2, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Apprentice – Document Control (Quality / Compliance Support)

Company

Piramal Critical Care (Piramal Pharma Ltd.)

Location

Digwal, Telangana, India

Employment Type

Full-time (Apprenticeship)

Job Posting

Posted yesterday
Application deadline: July 31, 2026


Division

Piramal Critical Care (PCC)


Role Summary

This is an entry-level apprenticeship role focused on document control, quality system support, and compliance documentation in a pharmaceutical manufacturing environment. The role ensures proper issuance, maintenance, archiving, and retrieval of controlled documents such as SOPs, batch records, and logbooks.


Key Responsibilities

Document Control & Management

  • Manage document control system including issuance, archival, retention, and destruction

  • Issue and distribute:

    • SOPs (Standard Operating Procedures)

    • STPs (Standard Test Procedures)

    • Batch records

    • Worksheets and logbooks

  • Ensure proper version control and retrieval of documents

  • Remove obsolete SOP copies before issuing updated versions

  • Maintain document layouts, specifications, and test procedures

  • Issue and manage shade cards for QC (Quality Control)

  • Archive completed logs after verifying completeness

  • Retrieve documents as required for audits or operational needs


Compliance & Quality Support

  • Ensure adherence to documentation standards and GMP practices

  • Support audit readiness through proper document maintenance

  • Participate in compliance activities within QC/QA systems

  • Maintain accuracy and traceability of all controlled documents


Safety Responsibilities

  • Identify unsafe conditions and unsafe acts

  • Report incidents, accidents, near misses, or illness

  • Support corrective and preventive actions (CAPA)

  • Follow workplace safety protocols and escalate risks appropriately


Administrative & Support Tasks

  • Shredding of obsolete or confidential documents

  • Supporting departmental documentation needs

  • Perform any additional tasks assigned by manager or HOD


Educational Qualification

  • Not strictly specified (typically Diploma / B.Sc / relevant freshers eligible depending on company apprenticeship rules)


Experience Required

  • Entry-level (fresher / no prior experience required)


Skills Required

  • Basic understanding of documentation systems

  • Attention to detail

  • Ability to follow SOPs strictly

  • Organizational skills

  • Awareness of GMP and safety practices (preferred)

  • Basic communication skills


Work Environment

  • Pharmaceutical manufacturing / QC documentation environment

  • Highly regulated (GMP-compliant) setting

  • Structured and process-driven work


Core Role Summary (Simple View)

This job is mainly about:

  • Managing pharma documentation systems

  • Handling SOPs, batch records, logbooks

  • Ensuring version control and compliance

  • Supporting QC/QA documentation workflows

  • Following strict GMP and safety procedures


Career Nature

This is a pure entry-level pharma operations / quality documentation apprenticeship, not a research or clinical role.

It can lead to:

  • QA Documentation Executive

  • QC Analyst (if lab transition happens)

  • GMP Compliance roles

  • Manufacturing quality systems roles