Website:
Job details:
Company Description EUGIA SL is a Spain-based company headquartered on Avenida Basagoiti Etorbidea, 69, in Getxo, Vizcaya. While its origins are in the restaurant sector, the organization is expanding into the pharmaceutical industry, with a focus on injectable products. The company is building capabilities to support high-quality, compliant manufacturing operations. Team members can expect a growing, international environment with evolving processes and opportunities to contribute to new business lines. EUGIA SL values professionalism, safety, and adherence to industry standards as it develops its pharmaceutical portfolio.
Role Description This is a full-time, on-site role based in Hyderabad, focused on injectable pharmaceutical operations. The role involves supporting day-to-day manufacturing activities for injectable products, ensuring compliance with Good Manufacturing Practice (GMP) and internal quality standards. Responsibilities include coordinating with production and laboratory teams, assisting in process documentation, monitoring batch records, and participating in in-process checks to maintain product safety and efficacy. The position may also involve collaborating with quality assurance, regulatory, and supply chain teams to support smooth operations and readiness for audits and inspections. The role requires active participation in continuous improvement initiatives and effective communication with cross-functional colleagues.
Qualifications
- Candidates should possess strong domain knowledge in Pharmacy and Pharmaceuticals, including understanding of injectable formulations and dosage forms.
- Candidates should possess practical Laboratory Skills related to sterile manufacturing, basic analytical techniques, and documentation of test results.
- Candidates should possess a solid understanding of Good Manufacturing Practice (GMP) and other relevant regulatory and safety guidelines for injectable products.
- Candidates should possess Sales or commercial awareness skills to effectively support product positioning, customer interactions, or cross-functional collaboration with commercial teams, if required.
- Relevant qualifications such as a degree in Pharmacy, Pharmaceutical Sciences, or a related field; prior experience in injectable or sterile manufacturing is highly beneficial.
- Strong attention to detail, ability to follow standard operating procedures, good communication skills, and the capacity to work collaboratively on-site in a regulated environment.
- Comfort with using basic computer applications for record keeping and familiarity with quality systems or ERP tools is an advantage.
Click on Apply to know more.