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Senior 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: Senior Executive – Quality Control (QC)
Company: Piramal Pharma Solutions (PPS), Navi Mumbai, Maharashtra, India
Job Type: Full-Time | Experienced | Onsite
Job ID: 9848
Application Deadline: 20/12/2025

About Piramal Pharma Solutions (PPS):
Piramal Pharma Solutions (PPS), part of the globally recognized Piramal Group, is a leading Contract Development and Manufacturing Organization (CDMO) offering end-to-end pharmaceutical solutions. With a globally integrated network across North America, Europe, and Asia, PPS provides services spanning drug discovery, process and pharmaceutical development, clinical trial supplies, and commercial production of APIs and finished dosage forms. PPS specializes in high-potency APIs, antibody-drug conjugates, sterile fill/finish, peptide products, potent solid oral drugs, and biologics including vaccines, gene therapies, and monoclonal antibodies.

Role Overview:
Piramal Pharma Solutions is seeking a Senior Executive – QC to join our Navi Mumbai facility. The role is ideal for candidates with prior experience in analytical testing, stability studies, and quality compliance in a cGMP environment. The incumbent will be responsible for sampling and analysis of in-process, intermediate, and stability samples, preparation of protocols and reports, and supporting the quality control team to maintain compliance and operational excellence.

Key Responsibilities:

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

  • Perform sampling, charging, and withdrawal of stability samples.

  • Prepare and maintain stability protocols, reports, and hold time study documentation.

  • Ensure accurate and compliant record-keeping for all analytical activities.

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

  • Support the QC team in maintaining efficiency, quality, and compliance.

  • Execute additional tasks assigned by senior management.

Qualifications & Experience:

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

  • Previous experience in pharmaceutical quality control or analytical testing is preferred.

  • Strong knowledge of cGMP standards, laboratory SOPs, and analytical documentation practices.

Skills & Competencies:

  • Attention to detail, accuracy, and scientific rigor.

  • Ability to manage multiple tasks while ensuring compliance and quality.

  • Strong communication and teamwork skills.

  • Proficiency in laboratory operations and documentation practices.

Why Join PPS:

  • Work with a leading global CDMO with exposure to diverse pharmaceutical technologies.

  • Contribute to high-impact projects supporting drug development and manufacturing.

  • Opportunity for professional growth within a structured, globally integrated organization.

  • Be part of a company committed to ethical practices, inclusivity, and equal employment opportunity.

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

Location:
Piramal, Thane, Maharashtra, 400703, India

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