Description
Job Summary:
Quality Inspector for a veterinary pharmaceutical laboratory, responsible for inspecting routines, documents, equipment, and processes to ensure compliance and continuous improvement.
Key Highlights:
1. Working within a leading group in veterinary pharmaceutical compounding
2. Focus on ensuring unmatched rigor and precision in sterile compounding
3. Opportunity to ensure quality and compliance in the laboratory
**Atlas Pharma S.A.** is a leading group and holder of **major brands**, specialized in the pharmaceutical compounding market.
Its founding brand is **DrogaVET**, recognized as Brazil's pioneering, leading, and largest network of compounding pharmacies **exclusively dedicated to veterinary medicine**. Its mission is clear: to provide the most effective treatment for animals and ensure maximum confidence and peace of mind for their caregivers, elevating standards in veterinary compounding.
Completing its portfolio, **Neuvye** originated in ophthalmology, which led it to develop an **exceptional level of rigor and precision in sterile compounding**. This quality methodology permeates every stage—from the rigorous selection and qualification of raw materials to final quality control—ensuring the highest degree of care and attention in each product.
**What’s the opportunity?**
Quality Inspector \- Campo Largo
**What will you do?**
* Conduct routine inspections across all laboratory processes, ensuring adherence to SOPs and internal standards.
* Verify records, results, reports, and documents to ensure traceability and compliance.
* Monitor equipment usage, cleaning, and calibration.
* Inspect raw materials, supplies, and laboratory materials, evaluating integrity, batch number, expiry date, and compliance.
* Assess execution of processes such as weighing, preparation, fractionation, analyses, and internal testing.
* Track and document non-conformities (NCRs), participate in root cause investigations, and support corrective/preventive actions.
* Audit compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and biosafety regulations.
* Monitor and track departmental quality indicators.
* Train and guide staff on standards, protocols, and quality requirements.
* Ensure compliance during internal and external audits.
* Support validations, equipment qualification, and continuous process improvement.
**If this interests you, check whether you meet the requirements:**
* Completed High School education.
* Preferred: Technical degree in Chemistry, Pharmacy, Biotechnology, Quality Control, or related fields.
* Experience in laboratories, quality control, or inspection will be considered an advantage.
**Requirements:**
* Experience in laboratories, quality control, or inspection will be considered an advantage.
* Knowledge of Good Laboratory Practices.
* Basic knowledge of metrology and equipment calibration.
* Basic computer skills (spreadsheets, traceability systems, and recordkeeping).
**Learn more about this position:**
Work schedule: Monday to Friday, from 8:00 AM to 12:00 PM and from 1:00 PM to 5:48 PM.
**Benefits:**
Meal or food allowance of R$ 1\.100,00 per month, with a R$ 10,00\ deduction.
Unimed health insurance after 3 months.
Emotional well-being program \- OPTUM.
SESC membership.
Discount on compounded medications.
Birthday day off, subject to eligibility criteria.
USP and FATEC partnership agreements.
Christmas kit.
Commemorative gifts.
Childcare reimbursement.
Online DrogaVET store discount.