Apprentice

PeopleStrong; North Goa; On-site; INR 300,000 - 600,000; Full time

Job summary

PeopleStrong is seeking a QA/document control professional in Goa to manage SOPs, master lists, document control, and calibration reviews. The role supports batch manufacturing, data trending for QMS events, and timely QA reviews.

You will ensure proper data backup, logbook maintenance, and periodic revisions of essential documents while coordinating with the QA function to maintain compliance and traceability.

Responsibilities

• Review daily trends (EM/water).
• Conduct particle count in the facility as per schedule.
• Ensure smooth execution of document issuance, distribution, control, retrieval and data backup (Scanning) of relevant documents.
• Updation of master list of SOPs, SAP and TDS, and Equipment and logbooks as activities occur.
• Tracking of all master documents with respect to periodic revision (e.g. SOP, SAP & TDS, Equipment).
• Trending of data related to QMS events for evaluation.
• Tracking of activities assigned to QA function for timely review.
• Support in dispensing and facility monitoring during batch manufacturing.
• Review of calibration records and schedule.

Job description

1. Affix Master, Controlled copy, Obsolete, Issued by stamp on respective documents and signing.
2. Issuance of logbooks, formats as per requirement
3. Review of daily trends (EM/water)
4. Conducting particle count in the facility as per schedule.
5. Ensure smooth execution of document issuance, distribution, control, retrieval and data backup (Scanning) of relevant documents
6. Updation of master list i.e. master list of SOP, master List of SAP and TDS & master list of Equipment and logbooks as and when activities are performed.
7. Tracking of all master documents w.r.t their periodic revision. e.g. Master list of SOP, Master list of SAP & TDS & Master list of Equipment.
8. Trending of data related to QMS events for evaluation.
9. Tracking of activities assigned to QA function for timely review.
10. Support in dispensing and facility monitoring during batch manufacturing
11. Review of calibration records and schedule