Kevin Process Technologies
Website:
kevin.in
Job details:
Company Description Kevin Process Technologies is a specialized partner to pharmaceutical manufacturers, focused exclusively on granulation and coating in solid oral dosage production. With over thirty years of experience, the company supports critical stages where product quality is most often determined, including content uniformity, dissolution performance, and coating behavior. Kevin provides end-to-end process development services, working alongside client R&D and tech-transfer teams to develop, optimize, and scale robust processes. The company also designs and supplies cGMP-compliant, audit-ready equipment such as rapid mixer granulators, fluid bed processors, roll compactors, and tablet coaters. Kevin is known for engineering solutions around real manufacturing challenges to help clients achieve reliable, regulatory-compliant outcomes.
Role Description The QC Manager is a full-time, on-site role based in Ahmedabad, responsible for overseeing quality control activities for solid dosage process development and equipment manufacturing. This role includes planning, organizing, and supervising QC tests and inspections on raw materials, in-process samples, and finished products to ensure compliance with cGMP and internal quality standards. The QC Manager will review and approve analytical results, specifications, and COAs; investigate non-conformities; and coordinate corrective and preventive actions. The role involves close collaboration with production, R&D, and regulatory teams to support validation, tech-transfer, and audit readiness. The QC Manager will also train and mentor QC staff, maintain documentation and laboratory systems, and support continuous improvement of quality processes.
Qualifications
- Strong knowledge of pharmaceutical QC practices, cGMP requirements, and regulatory expectations for solid oral dosage forms.
- Experience with analytical testing methods relevant to granulation and coating processes, including dissolution, content uniformity, and related quality attributes.
- Proficiency in quality systems management, including documentation control, deviation handling, CAPA, change control, and audit preparation.
- Ability to lead and develop a QC team, allocate workloads, and ensure adherence to safety standards.
- Effective communication and collaboration skills for working with production, R&D, engineering, and regulatory stakeholders.
- Bachelor’s or Master’s degree in Mechanical, Production or a related scientific discipline.
- Relevant experience in pharmaceutical machine manufacturing or equipment-based process environments; exposure to solid dosage process development is an advantage.
- Strong attention to detail, problem-solving aptitude, and capability to make data-driven decisions under time constraints.
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