We are looking for Computer Operators to support the QA / documentation team at our WHO-GMP certified manufacturing plant. The role mainly involves data entry, record-keeping, and document issuance under proper guidance. Full training will be provided, so it suits candidates who are good with computers and want a stable, long-term job in pharma.
Key Responsibilities
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Data entry and maintenance of records in MS Excel / Word and company software.
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Issue and maintain controlled documents such as logbooks, formats, and batch records (BMR/BPR) as per instructions.
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Maintain control sample records and registers accurately.
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Keep proper filing of documents — both physical and digital — with correct numbering and tracking.
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Print, scan, photocopy, and manage documents as required.
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Update daily/weekly status and basic MIS reports.
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Follow good documentation practices and maintain confidentiality of company records.
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Coordinate with QA and other departments for document requirements and follow-ups.
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Education: 12th pass / Graduate (any stream).
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Experience: Freshers welcome. 0–2 years in computer operator / data entry / back-office work.
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Skills:
- Good typing speed with accuracy.
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Working knowledge of MS Excel, Word, and email.
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Neat record-keeping and strong attention to detail.
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Clear communication in Hindi & basic English.
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Personal Traits:
- Disciplined, sincere, and reliable.
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Looking for a long-term, stable role.
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Willing to learn and follow SOPs and instructions.
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Salary as per industry norms
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Full on-the-job training in pharma documentation practices
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Health & accidental insurance (self & family), PF/ESIC as per norms
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Subsidised meals & company transport
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Stable, long-term career in a WHO-GMP certified plant
