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Executive-Qc

0-2 years
Not Disclosed
10 Nov. 26, 2025
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

Job Title: Executive – Quality Control (QC)
Company: Piramal Pharma Solutions (PPS), Navi Mumbai, Maharashtra, India
Job Type: Full-Time | Experienced | Onsite
Job ID: 9846
Application Deadline: 20/12/2025

About Piramal Pharma Solutions (PPS):
Piramal Pharma Solutions (PPS), a division of the Piramal Group, is a global Contract Development and Manufacturing Organization (CDMO) delivering end-to-end pharmaceutical solutions across the drug lifecycle. With integrated facilities across North America, Europe, and Asia, PPS offers comprehensive services including drug discovery, process and pharmaceutical development, clinical trial supplies, and commercial manufacturing of APIs and finished dosage forms. PPS specializes in high-potency APIs, antibody-drug conjugates, sterile fill/finish, peptide products, and potent oral solid formulations. The company also provides biologics development and manufacturing, including vaccines, gene therapies, and monoclonal antibodies.

Role Overview:
Piramal Pharma Solutions is seeking a motivated Executive – QC to join our Navi Mumbai facility. This role is ideal for candidates with strong analytical skills, attention to detail, and experience in cGMP-compliant quality control operations. The Executive – QC will perform analysis and sampling of in-process, intermediate, and stability samples while ensuring accurate documentation and supporting quality compliance initiatives.

Key Responsibilities:

  • Conduct analysis of in-process, intermediate, and stability samples following SOPs and cGMP guidelines.

  • Perform charging, withdrawal, and analysis of stability and hold-time study samples.

  • Prepare and maintain stability protocols and reports with accuracy and compliance.

  • Maintain comprehensive documentation as per regulatory and cGMP requirements.

  • Handle delegated responsibilities of the reporting authority in their absence.

  • Support senior QC staff and execute additional analytical or administrative tasks as assigned.

Qualifications & Experience:

  • Master’s or Bachelor’s degree in Chemistry or a related scientific field.

  • Prior experience in pharmaceutical quality control, analytical testing, or cGMP-compliant laboratory operations is advantageous.

Skills & Competencies:

  • Strong analytical and observational skills with meticulous attention to detail.

  • Knowledge of laboratory procedures, QC standards, and documentation practices.

  • Ability to manage multiple tasks while maintaining high quality standards.

  • Excellent communication and teamwork skills.

Why Join PPS:

  • Be part of a leading global CDMO supporting drug development and manufacturing worldwide.

  • Gain exposure to diverse pharmaceutical technologies and high-impact projects.

  • Develop professionally in a structured, collaborative, and globally integrated environment.

  • Work with an organization committed to ethical practices, inclusion, and equal opportunity employment.

Equal Employment Opportunity:
Piramal Pharma Solutions is an Equal Employment Opportunity and Affirmative Action employer. All employment decisions are based on qualifications, skills, performance, and merit, without discrimination based on legally protected characteristics.

Location:
Piramal, Thane, Maharashtra, 400703, India

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