About GELIKAPS LIFESCIENCES LTD.

Gelikaps Lifesciences Ltd. , formerly known as Dinesh Remedies Limited , is a GMP-certified manufacturer of Empty Hard Gelatin Capsules , serving customers across the pharmaceutical, nutraceutical, herbal, and healthcare industries.

We are seeking a Junior QA Assistant to support our Quality Assurance function and contribute to maintaining GMP compliance, accurate documentation, and effective quality-system practices across our manufacturing operations.

About the Role The Junior QA Assistant will support the Quality Assurance team in routine GMP compliance, quality documentation, record review, shop-floor QA activities, and coordination with other departments .

The position offers an opportunity to develop practical experience in Quality Assurance within a regulated manufacturing environment.

Key Responsibilities

- Support day-to-day Quality Assurance activities under the direction of the QA team.
- Assist with preparation, review, and maintenance of quality-related documentation and records.
- Review assigned Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), logbooks, checklists, and related documents for completeness and accuracy.
- Support routine GMP compliance activities within manufacturing and operational areas.
- Assist with line clearance, in-process checks, area inspections, and shop-floor QA activities , as assigned.
- Maintain and update QA registers, records, formats, and controlled documents.
- Assist with documentation related to deviations, CAPA, change controls, incidents, and other quality-system activities .
- Coordinate with Production, QC, Warehouse, Engineering, and other departments on routine QA requirements.
- Assist the QA team in preparing documentation and records for internal, customer, and regulatory audits.
- Follow approved SOPs, procedures, documentation practices, and applicable GMP requirements.




- Identify documentation discrepancies and escalate quality-related issues to the appropriate QA personnel.
- Maintain proper organization, traceability, and confidentiality of quality records.
- Perform other QA responsibilities assigned by the QA management team.

Required Qualifications & Skills
- Bachelor's degree in Pharmacy, Chemistry, Microbiology, Life Sciences, or a related discipline .
- Relevant experience in Quality Assurance, Quality Control, pharmaceutical manufacturing, or a related regulated manufacturing environment will be an advantage.
- Basic knowledge of GMP, Good Documentation Practices (GDP), SOPs, and pharmaceutical quality systems .
- Strong attention to detail and accuracy in documentation.
- Positive written and verbal communication skills.
- Basic proficiency in MS Office, particularly Microsoft Word and Excel .
- Ability to follow established procedures and maintain accurate records.
- Ability to coordinate effectively with cross-functional teams.
- Willingness to work on-site at Padra, Gujarat .

Preferred Qualifications
- Practical or academic exposure to pharmaceutical manufacturing and QA activities.
- Familiarity with BMR/BPR review, deviations, CAPA, change control, SOPs, line clearance, and GMP documentation .
- Previous experience in pharmaceutical, nutraceutical, healthcare, chemical, or other regulated manufacturing environments.
- Candidates who can join immediately or within 15 days will be preferred.

What We Offer An opportunity to develop practical expertise in GMP compliance, Quality Assurance systems, pharmaceutical manufacturing documentation, audit readiness, and cross-functional quality operations within a growing manufacturing organization.

Application

Interested candidates may share their updated CV with:

- Current CTC, if applicable
- Expected CTC
- Notice period
- Current location
- Availability for an interview

Location: Padra, Gujarat, India Workplace: On-site

- Employment Type: Full-time

📌 Junior QA Assistant (Padra)
🏢 Gelikaps lifesciences
📍 Padra