Rivpra Walk-In QA, QC, Production, F&D, ADL, IPQA

Rivpra Formulation Pvt. Ltd., a WHO-cGMP certified pharmaceutical company, is conducting a walk-in drive for multiple vacancies across IPQA, QA, QC, Production, F&D, and ADL departments. The company is hiring both freshers and experienced professionals for roles such as Trainee, Officer, Sr. Executive, and Assistant Manager. Candidates from B.Pharm, M.Pharm, B.Sc, Microbiology, and B.Tech backgrounds are eligible. This hiring drive will take place on 12th April 2026 at Haridwar, offering excellent opportunities for candidates looking to build a stable career in pharmaceutical manufacturing and research.

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Company Overview

Rivpra Formulation Pvt. Ltd. is a rapidly growing pharmaceutical manufacturing company with a WHO-cGMP compliant facility located in Haridwar. The company is known for delivering high-quality pharmaceutical formulations while maintaining strict adherence to global regulatory standards.

With a strong focus on innovation, compliance, and operational excellence, Rivpra provides a dynamic work environment where professionals can gain hands-on exposure to advanced manufacturing systems, analytical laboratories, and formulation development processes.

The company continues to expand its footprint in regulated and semi-regulated markets, contributing to global healthcare by ensuring safe, effective, and affordable medicines.

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Job Role & Responsibilities

Rivpra is hiring across multiple departments, each offering specialized roles in pharmaceutical manufacturing, quality assurance, and research.

Production Department (Trainee – Freshers)

• Assist in manufacturing of oral solid dosage forms
• Support granulation, compression, and coating processes
• Follow GMP guidelines and SOP compliance
• Maintain batch manufacturing records (BMR)
• Ensure cleanliness and safety in production areas

Quality Assurance (QA – Trainee)

• Assist in documentation and quality systems (QMS)
• Support IPQA activities and compliance checks
• Maintain SOPs and validation records
• Participate in audits and regulatory inspections

IPQA (Officer)

• Monitor in-process quality checks
• Ensure compliance with cGMP standards
• Perform line clearance and documentation verification

Quality Control (QC – HPLC / Microbiology)

• Perform analysis using HPLC and other analytical instruments
• Conduct microbiological testing and environmental monitoring
• Maintain GLP compliance and documentation
• Handle calibration and maintenance of lab instruments

F&D (Formulation & Development)

• Develop and optimize pharmaceutical formulations
• Conduct trials for product development and scale-up
• Prepare development reports and regulatory documents

ADL (Analytical Development Lab)

• Develop analytical methods for drug products
• Perform validation and stability studies
• Support regulatory submissions with analytical data

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Eligibility / Qualifications

Educational Qualification:

B.Pharm, M.Pharm, B.Sc (Chemistry, Life Sciences), Microbiology, B.Tech

Experience:

• Freshers: Eligible for Production and QA Trainee roles
• 1–3 Years: IPQA Officers, F&D Trainee/Officer, ADL roles
• 2–4 Years: QC HPLC roles
• 4–6 Years: Senior roles in F&D and ADL

Required Skills:

• Knowledge of pharmaceutical manufacturing and quality systems
• Understanding of GMP, GLP, and regulatory compliance
• Experience with analytical instruments like HPLC
• Strong documentation and data handling skills
• Ability to work in a team-based pharma environment

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Location & Salary

Job Location:

Rivpra Formulation Pvt. Ltd., Haridwar, Uttarakhand

Salary:

Compensation will be offered based on experience and industry standards. Freshers can expect structured training programs along with career growth opportunities in pharmaceutical production and quality functions.

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Application Process

Candidates can attend the walk-in interview directly or explore company details through the official website.

Walk-In Details:

• Date: 12th April 2026 (Sunday)
• Candidates are advised to check timing details with HR or website
• Location: Haridwar (WHO-cGMP Facility)

Documents Required:

• Updated Resume
• Educational Certificates
• ID Proof
• Experience Certificates (if applicable)

Contact / Website:

• Website: rivpraformulation.com

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Why Join Rivpra Formulation Pvt. Ltd.

Rivpra offers a strong platform for both freshers and experienced professionals to grow in the pharmaceutical industry. Employees gain exposure to modern manufacturing practices, regulatory compliance, and analytical research, which are critical for building long-term careers.

Key benefits include:

• WHO-cGMP certified manufacturing facility
• Fast-growing pharma company with expansion plans
• Learning-driven work culture
• Exposure to advanced pharmaceutical technologies
• Opportunities in QA, QC, Production, and R&D

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Frequently Asked Questions (FAQs)

1. Who can apply for Rivpra jobs?

Candidates with B.Pharm, M.Pharm, B.Sc, Microbiology, or B.Tech qualifications can apply.

2. Are freshers eligible?

Yes, freshers can apply for Production and QA trainee roles.

3. What is the selection process?

Candidates need to attend the walk-in interview with required documents.

4. What departments are hiring?

IPQA, QA, QC, Production, F&D, and ADL departments.

5. Is experience mandatory for all roles?

No, some roles are open for freshers, while others require 1–6 years of experience.

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Summary

Company	Rivpra Formulation Pvt. Ltd.
Vacancies	Trainee, Officer, Sr. Executive, Assistant Manager (QA, QC, Production, F&D, ADL, IPQA)
Required Education	B.Pharm, M.Pharm, B.Sc, Microbiology, B.Tech
Experience	Freshers to 6 Years