Trainee - QA

Piramal Pharma Limited; Zone 1 Tiruvottiyur; On-site; INR 200,000 - 300,000; Full time

Job summary

Piramal Pharma Limited is seeking a Trainee - QA to join our QA team in India. The role focuses on assisting in review of batch records, supporting inspections, and aiding in SOP preparation to ensure quality compliance in a pharmaceutical setting.

The successful candidate will have a Master's in Chemistry with 0–1 year of experience, strong communication skills, and proficiency in MS Office. This entry-level position offers learning and growth in a global CDMO environment.

Qualifications

• Master's degree in Chemistry with 0–1 year of experience 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.

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.

Skills

Communication

Teamwork

Attention to detail

Education

Master's in Chemistry

Tools

MS Office

Job description

Job Title Trainee - QA

Be the First to Apply Division Piramal Pharma Solutions Piramal 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 Description

• 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.

Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group. PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.