Description
Job Summary:
A professional to support quality assurance, ensuring compliance and continuous improvement of Pharmédice’s processes — a leader in sterile drug compounding.
Key Highlights:
1. Work for a leading company in sterile drug compounding.
2. A team of champions with excellence embedded in its DNA and a focus on access to medications.
3. A top-tier professional ready to make a difference in national growth.
**About the Company**
**If you are an energetic, determined professional who loves challenges, join Pharmédice — a leader in sterile drug compounding.**
Founded in Minas Gerais, Pharmédice Manipulações Especializadas redefines excellence in sterile drug compounding for human health. Pharmédice not only meets the industry’s highest compounding standards but elevates them to a new level. We combine regulatory rigor, intelligent use of data, and unmatched expertise to deliver sterile medications rapidly and with exceptional quality.
A team of champions carrying excellence in their DNA — composed of pharmacists specialized in various fields, technicians, specialists, engineers, analysts, supervisors, IT professionals, commercial staff, logistics and procurement personnel. All united by a single purpose: **ensuring market access to hard-to-obtain medications.**
**So, if you believe you are a top-tier professional ready to make a difference in our structure and national growth, join us!**
**Job Description**
Support the organization’s processes, products, and services in meeting quality requirements established by internal standards, applicable legislation, and current certifications; manage documentation control and monitor key performance indicators, ensuring compliance and continuous process improvement.
**Responsibilities and Duties**
* Physicochemical analyses of raw materials, finished products, and packaging materials;
* Water analysis;
* Preparation of reagent solutions and analytical standards;
* Sampling of raw materials and packaging materials;
* Recording, evaluating, and reporting analytical results;
* Assisting in deviation investigations, Out-of-Specification (OOS) results, and nonconformities.
**Requirements and Qualifications**
**Education:** Technical-level qualification (Pharmacy, Chemistry, Biotechnology, or related fields). Pursuing a bachelor’s degree (up to sixth semester preferred). Solid experience with HPLC.
**Experience:** Prior experience in Quality Assurance, preferably in industrial or pharmaceutical companies.
**Technical Knowledge:**
* Quality Management Systems (ISO 9001, GMP, HACCP, or equivalents)
* Quality Tools (5W2H, PDCA, Ishikawa, MASP, Pareto, etc.)
* Document control and audits
* Interpretation of applicable standards and legislation
* Microsoft Office Suite (intermediate to advanced level)
* Mandatory HPLC equipment experience — data evaluation and processing using Empower software (Waters)
**Benefits**
* Meal Allowance: BRL 23.00/day
* Transportation Allowance / Fuel Allowance
* UsiSaúde Health Plan (no monthly fee, only co-payment)
* Dental Plan: BRL 26.00/month (optional)
* Working hours: 08:00–17:48, Monday to Friday
* SESC and Pharmacy Agreements
Employment Type: Permanent CLT
Working Hours: Monday to Friday, 08:00–17:48
Employment Type: Full-time
**Required Experience:**
* Operation of HPLC equipment (Mandatory)
* Minimum 3 years in a compounding laboratory (Mandatory)
Employment Type: Full-time, Permanent CLT
Salary: BRL 2,594.00 – BRL 2,600.00 per month
Work Location: On-site