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Officer

Hetero
Hetero
1-4 years
Not Disclosed
10 Jan. 15, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Officer – Quality Control / Analytical Laboratory

Location: Penjerla, Hyderabad, Telangana, India
Employment Type: Permanent
Industry: Pharmaceutical / Biopharmaceutical
Experience Required: 1–4 Years (Plasma Products experience preferred)


Job Overview

We are hiring an Officer – Quality Control (QC) / Analytical Laboratory to support routine analytical testing and laboratory compliance activities at our Penjerla, Hyderabad facility. The role is ideal for professionals with hands-on experience in pharmaceutical or biopharmaceutical quality control, particularly those familiar with plasma-derived products and regulated laboratory environments.

The position offers a permanent opportunity to work within a GMP-compliant setup, ensuring analytical accuracy, regulatory compliance, and data integrity.


Key Responsibilities

  • Perform routine analytical testing for pharmaceutical and biopharmaceutical products, with preference for experience in plasma-derived products.

  • Operate and maintain laboratory instruments including UV Spectrophotometer, pH Meter, Weighing Balance, Kjeldahl apparatus, and HPLC.

  • Execute analytical method validations in accordance with approved protocols, regulatory guidelines, and internal quality systems.

  • Ensure strict adherence to Good Laboratory Practices (GLP) to maintain data reliability and laboratory compliance.

  • Maintain accurate, complete, and compliant records in line with Good Documentation Practices (GDP).

  • Document analytical results, method validation data, instrument usage, calibration, and maintenance activities.

  • Support audits, inspections, and internal quality reviews by providing required documentation and technical inputs.

  • Follow safety, quality, and compliance procedures as per company and regulatory standards.


Required Qualifications and Experience

  • Education: B.Pharm, M.Pharm, B.Sc., M.Sc., or equivalent qualification in a relevant scientific discipline.

  • Experience: 1 to 4 years of experience in a pharmaceutical or biopharmaceutical analytical/QC laboratory.

  • Prior exposure to plasma products or biological products will be an added advantage.

  • Hands-on experience with analytical instruments, especially HPLC and UV spectroscopy.

  • Sound knowledge of GLP, GDP, and basic regulatory requirements.

  • Ability to work independently as well as in a team-oriented, regulated environment.


Key Skills and Competencies

  • Quality Control Testing

  • Analytical Instrumentation

  • Method Validation

  • GLP and GDP Compliance

  • HPLC and UV Spectroscopy

  • Pharmaceutical Documentation

  • Regulatory Compliance


Why Join This Role?

  • Permanent opportunity in a regulated pharmaceutical environment

  • Exposure to plasma and biopharmaceutical product testing

  • Strong learning and career growth prospects in quality and analytics

  • Work location in one of India’s major pharmaceutical hubs


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