Quality Control Officer

The Quality Control Officer will be responsible for performing analysis of raw materials, in-process samples, and finished products, ensuring compliance with GMP and GLP standards. The involves maintaining laboratory documentation, handling analytical instruments, and supporting quality investigations and audits. The candidate will work closely with QA and production teams to ensure consistent product quality and regulatory compliance.

Roles and Responsibilities:

• Perform analysis of raw materials, in-process samples, and finished products as per specifications.
• Conduct routine and non-routine laboratory testing using standard analytical methods.
• Operate and maintain laboratory instruments such as HPLC, GC, UV, and other equipment.
• Ensure compliance with GMP, GLP, and regulatory quality standards.
• Maintain accurate laboratory records, test reports, and documentation.
• Perform calibration and routine maintenance of laboratory instruments.
• entify out-of-specification (OOS) results and assist in investigations and root cause analysis.
• Coordinate with QA and production teams to resolve quality-related issues.
• Monitor environmental conditions within the laboratory as per required standards.
• Ensure proper handling, storage, and disposal of chemicals and samples.
• Participate in internal audits and support external regulatory inspections.
• Maintain inventory of laboratory reagents, chemicals, and consumables.
• Follow safety protocols and ensure a safe working environment in the laboratory.
• Support stability studies and method validation activities.
• Contribute to continuous improvement initiatives for quality and efficiency.

Stivaph Healthcare Pvt. Ltd. is an Indian pharmaceutical manufacturer and supplier based in Ahmedabad, Gujarat. Established in December 2019, the company specializes in third-party manufacturing and global exports, delivering a wide range of affordable and effective medicinal formulations.

Our Story

Since its inception, Stivaph Healthcare has focused on building a strong presence in pharmaceutical manufacturing by combining quality-driven processes with global compliance standards. With a commitment to affordability and accessibility, the company has expanded its reach to over 15 countries across Africa, Southeast Asia, the Middle East, and Latin America.

Our Mission

• To deliver affordable and effective pharmaceutical formulations globally
• To maintain high standards of quality, safety, and compliance
• To support partners with reliable contract manufacturing solutions
• To expand access to essential medicines across international markets

Our Vision

To be a trusted global pharmaceutical manufacturing partner known for quality, reliability, and innovation.

Our Services / What We Offer

Stivaph Healthcare provides comprehensive pharmaceutical solutions, including:

• Third-party (contract) manufacturing for domestic and international clients
• Loan license manufacturing services
• P2P (Product-to-Product) manufacturing solutions
• Export of pharmaceutical products to global markets

Our Product Portfolio

The company offers a diverse range of formulations:

• Solid Orals – Tablets and capsules
• Liquid & Topical – Liquid orals, ointments, and creams
• Specialized Segments – Antibiotics, anti-emetics, and skincare products

Why Choose Us

• WHO-GMP, EU-GMP, and PIC/S compliant manufacturing facility
• Presence in 15+ international markets
• Wide range of pharmaceutical formulations
• Strong focus on quality, safety, and regulatory compliance
• Experienced leadership with expertise in regulatory affairs
• Reliable and scalable contract manufacturing capabilities

Our Team

Stivaph Healthcare is led by Mr. Varun Bhupendrakumar Doshi, Managingector, who brings over 18 years of experience in regulatory affairs. The organization is supported by a team of approximately 50–100 professionals dedicated to quality manufacturing and global compliance.

Infrastructure / Technology

The company operates a modern manufacturing facility spread across 56,000 sq. ft. in Sanand GIDC II near Ahmedabad. The infrastructure is designed to meet international quality standards and is equipped to support large-scale pharmaceutical production.

Compliance & Certifications

Stivaph Healthcare adheres to global regulatory standards and holds multiple GMP certifications, including approvals from:

• Philippines FDA
• Regulatory authorities in Kenya, Yemen, Cambodia, and Nigeria

Our Commitment

Stivaph Healthcare Pvt. Ltd. is committed to delivering high-quality, safe, and effective pharmaceutical products. By combining advanced infrastructure, regulatory expertise, and a global outlook, the company ensures consistent value for its partners and customers.