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Piramal Pharma Ltd

Trainee - QA

Piramal Pharma Ltd Chennai, Tamil Nadu, India

Pharmaceutical Manufacturing · 1,001-5,000 employees

Yesterday
qa Junior (0-2 yrs) Full-time India
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About the role

The trainee will assist in reviewing batch production records, conducting inspections, and participating in deviation investigations. They will also support the preparation of SOPs and collaborate with various departments to ensure compliance with cGMP regulations.

What they look for

Quality Assurance Batch Production Records cGMP Regulations Standard Operating Procedures Internal Audits Pharmaceutical Manufacturing Documentation Microsoft Office Suite Communication Skills Teamwork Inspection Compliance

Requirements

Candidates should hold a Master's degree in Chemistry, with 0-1 year of experience in the pharmaceutical industry being a plus. Proficiency in Microsoft Office and strong communication skills are required for this role.

Full description

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Division

Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.  

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  

Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Trainee - QAJob Description

Responsible for executing QA related activity.Job Responsibilities:

  • Assist in the review and approval of batch production records and other manufacturing documentation.
  • Support the QA team in conducting in-process and final product inspections.
  • Participate in the investigation of deviations, non-conformances, and customer complaints.
  • Aid in the preparation and review of Standard Operating Procedures (SOPs) and other quality-related documents.
  • Assist in performing internal audits and supporting external audits as required.
  • Maintain accurate and organized quality records and documentation.
  • Collaborate with production, quality control, and other departments to ensure compliance with cGMP regulations.
  • Learn and apply quality assurance principles and best practices in a pharmaceutical setting.
  • Undertake any other tasks assigned by the QA management to support departmental objectives.

Job Qualifications:

  • Master's degree in Chemistry with 0-1 year of expeience in a pharmaceutical or related industry is a plus.
  • Excellent written and verbal communication skills.
  • Ability to work effectively both independently and as part of a team.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Eagerness to learn and develop a career in Quality Assurance within the pharmaceutical industry.

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