2022
Mepromax Lifesciences Pvt. Ltd., Dehradun, Uttarakhand
Quality Assurance Trainee
Quality · Compliance · Documentation
Quality assurance, without the complexity.
Practical QA, documentation and quality-system support for pharmaceutical, Ayurvedic, nutraceutical and related manufacturing businesses.
B.Sc. Pharmaceutical ChemistryD.Pharm — Ayurveda3+ Years QA Experience
Founded by Saumya Dubey, Founder & Lead QA Consultant.
B.Sc. Pharmaceutical ChemistryD.Pharm — Ayurveda3+ Years QA ExperienceSurat · Gujarat · India
Real QA Experience
Built from real QA work.
Qorivara is built on practical Quality Assurance experience across pharmaceutical environments. The work is grounded in records, review discipline, SOP control and the follow-through that manufacturing quality systems actually need.
Next
Unilever
Quality Assurance Officer
~6 months
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Quality Assurance Executive
Today
Qorivara Life Sciences
Founder & Lead QA Consultant
Surat, Gujarat
Documentation
The work is often in the details.
Qorivara supports the documents that slow teams down when they are outdated, incomplete or difficult to defend during review.
BMR / BPRSOPCOASpecificationsSTP / TDSBatch Record Review
Quality Systems
Quality systems need follow-through.
Internal audits, self-inspections, change-control records and monitoring documents all need disciplined closure, not just good intentions.
Internal AuditSelf InspectionChange ControlArea Monitoring
Services
Precise support for documentation-heavy QA work.
An editorial service list keeps the work scannable: numbers, thin dividers and expandable detail for the support a manufacturing team may actually need.
01BMR / BPRPreparation · Review · Revision
Support for batch manufacturing and packing records where accuracy, traceability and final-review confidence matter.
02SOPPreparation · Review · Revision
Practical cleanup and revision support so procedures stay current, readable and easier for teams to follow.
03Change ControlDocumentation · Structure · Follow-through
Help with change-control records and supporting documentation where scattered details need a clearer controlled path.
04Internal Audit & Self-InspectionGap review · Preparation · Action points
Focused review before pressure builds, turning visible gaps into practical follow-through actions.
05Specifications / STP / TDSTechnical consistency · Review · Cleanup
Review support for technical documents that need clearer wording, stronger consistency and fewer avoidable corrections.
06COA Preparation & ReviewCertificate review · Detail checks · QA handover
Preparation and review support for COAs where data presentation and quality review discipline need attention.
07Batch Record Final ReviewBacklog · Missing-entry checks · Release confidence
A disciplined second pass for teams that need batch records checked carefully without stretching internal QA further.
08Area Monitoring & QA DocumentationRecords · Logs · Quality-system support
Scoped support for area monitoring records and the supporting QA documentation that keeps quality systems traceable.
Industries
For regulated manufacturing businesses where quality records matter.
The strongest fit is a team that needs practical QA documentation support, sharper review discipline or temporary bandwidth around a clear requirement.
PharmaceuticalAyurvedic / HerbalNutraceuticalCosmetic / Related ManufacturingThird-Party / Private Label
Founder
Meet Saumya.
Founder & Lead QA Consultant
B.Sc. Pharmaceutical ChemistryD.Pharm — Ayurveda3+ Years QA Experience
Saumya's career began in hands-on QA roles and now continues through Qorivara Life Sciences in Surat. Her work is practical, document-aware and strongest where a business needs clear support without adding a large consulting layer.
Why Qorivara
A focused partner for the work that needs attention.
Direct Access
Clients work directly with Saumya Dubey, the founder and QA professional behind the work.
Focused Scope
Engagements stay close to the real bottleneck: records, SOPs, review pressure, audits or quality-system follow-through.
Practical Experience
The support is built from hands-on QA work across real manufacturing environments, not borrowed consulting theatre.
How It Works
Simple enough to start quickly. Structured enough to be useful.
Discuss
Start with the bottleneck, document type and business context.
Review
Review documents, records or quality-system areas creating friction.
Support
Revise, review or structure the work agreed at the start.
Deliver
Close with cleaned outputs, open issues and sensible next actions.
Remote Support
Documentation and review work that can often be handled digitally.
Useful for scoped SOP, BMR/BPR, COA, specification, STP/TDS and quality-system record review when secure document sharing is practical.
Hybrid Support
Assignments that may benefit from periodic site visits.
Some quality-system and audit-readiness requirements are better discussed with site context, depending on location, scope and confidentiality needs.
Contact
Have a QA requirement?
Tell Qorivara what you are working on and what support you need.
Surat · Gujarat · India