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Junior Executive

1-5 years
₹3.5–5.5 LPA
10 July 29, 2025
Job Description
Job Type: Full Time Education: B.Sc Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Junior Executive – DP Medical Device
Location: India
Company: Biocon Biologics Limited
Department: DP Medical Device
Job ID: 19397
Employment Type: Full-Time
Estimated Salary: ₹3.5–5.5 LPA (based on experience and industry standards)


Role Summary:
Biocon Biologics is hiring a Junior Executive to support documentation, compliance, and operational tasks in the DP Medical Device segment. The role emphasizes Good Documentation Practices (GDP), coordination for quality actions (Change Control, CAPA, Deviations), and meticulous handling of batch manufacturing and technical documentation.


Key Responsibilities:

Documentation & Records Management:

  • Requisition and receipt of BMRs (including additional pages) and execution checklists.

  • Receive and log document numbers and effective dates for technical documents, protocols, and reports.

  • Prepare, issue, revise, and archive logbooks, protocols, and technical reports.

  • Enter and maintain all logs related to the visual inspection area.

  • Review completed logbooks and arrange them for secure document storage.

Compliance & Quality Coordination:

  • Verify executed documents (BMRs) for accuracy and completeness.

  • Initiate and review Change Controls, CAPAs, and Events.

  • Track and close assigned quality actions in coordination with the QA department.

  • Assist in investigations and closure of deviations.

Process Adherence & Hygiene Compliance:

  • Maintain adherence to Good Documentation Practices (GDP) and hygiene standards.

  • Report illness or unhygienic practices as per company protocols.

  • Verify documents and annexures for completeness post-activity.


Candidate Profile:

  • Education: B.Sc. in Life Sciences, Biotechnology, or related field.

  • Experience: 1–5 years in pharmaceutical or medical device documentation, QA, or compliance.

  • Familiarity with Change Control, CAPA, Deviations, and GDP.

  • Strong organizational skills with attention to detail and regulatory adherence.

  • Proficient in documentation software and record maintenance.