Apprenticeship By Piramal Pharma Solutions
Apprenticeship By Piramal Pharma Solutions
Piramal Pharma Solutions (PPS), a part of the globally renowned Piramal Group, is a leading Contract Development and Manufacturing Organization (CDMO) providing end-to-end pharmaceutical solutions across the drug lifecycle. As a Quality Control (QC) Analyst Apprentice, you will play a vital role in supporting laboratory operations, ensuring product quality, and maintaining compliance with cGMP and international quality standards. This role involves analytical testing of finished goods, raw materials, and stability samples, along with meticulous documentation and adherence to regulatory requirements. It offers a unique opportunity to gain practical experience in a professional pharmaceutical environment committed to excellence, safety, and innovation.
Documents Required
Applicants submit the following documents:
  • Resume/CV
  • Valid Email ID
  • Mobile No.
  • Study Mark Sheets
  • Certificates (If you have)
  • Cover letter (If applicable)
  • Eligibility Criteria
    Applicants must meet the following criteria:
  • Educational Qualification: M.Sc. in Chemistry.
  • Candidates should demonstrate knowledge of analytical techniques and lab procedures.
  • Familiarity with cGMP, HSE, and data integrity standards is desirable.
  • Strong attention to detail, documentation accuracy, and adherence to safety protocols are essential.
  • Excellent communication and teamwork skills.
    Note: This apprenticeship is exclusively available in India. Specifically, in Mahad.
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    Responsibilities
    Interns will:
  • Conduct analysis of finished goods, stability samples, raw and packing materials, and in-process/cleaning samples.
  • Ensure proper calibration and maintenance of analytical instruments (e.g., HPLC, GC).
  • Prepare and maintain laboratory documentation, analytical data sheets, and Excel spreadsheets.
  • Record test results accurately and report findings to supervisors.
  • Manage working standards, reference materials, and analytical reagents.
  • Ensure compliance with 21 CFR Part 11 and Part 111 requirements.
  • Maintain good housekeeping and ensure safe laboratory practices (proper PPE usage, waste disposal, etc.).
  • Participate in quality events, deviations, and change controls as required.
  • Support equipment qualification, data entry in SAP, and document control activities.
  • Engage in cGMP and HSE training programs to uphold regulatory and quality standards.
  • How To Apply
    Follow the below steps to apply for the program:
    1. Visit Our Official Website.
    2. Read carefully all the information about the program details.
    3. Click on the "Register" to complete the registration with required details.
    4. After successful registration, Use the received credentials to log into your account.
    5. Once logged in, Click on the "Apply" button.
    6. You will be directed to the application form. Fill in all the required details accurately.
    7. Prepare the necessary documents as specified in the application requirements.
    8. Upload these documents in the designated sections of the application form.
    9. Before submitting, review all the information you have provided.
    10. After that, Click on the "Submit” button to submit your application.
    Note: "As a free user,"
    →'You're encouraged to share this valuable information with your friends to access the link properly'.

    Stipend

    Apprenticeship By Piramal Pharma Solutions
    SCHOLARSHIP PROVIDER
    Piramal Pharma Solutions
    APPLICATION DEADLINE
    09 November
    EDUCATION LEVEL
    Masters
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    Piramal Pharma Solutions (PPS), a part of the globally renowned Piramal Group, is a leading Contract Development and Manufacturing Organization (CDMO) providing end-to-end pharmaceutical solutions across the drug lifecycle. As a Quality Control (QC) Analyst Apprentice, you will play a vital role in supporting laboratory operations, ensuring product quality, and maintaining compliance with cGMP and international quality standards. This role involves analytical testing of finished goods, raw materials, and stability samples, along with meticulous documentation and adherence to regulatory requirements. It offers a unique opportunity to gain practical experience in a professional pharmaceutical environment committed to excellence, safety, and innovation.