Representante Comercial Farmacéutico - Región Bajío

Dünnpharma S.A. De C.V.; León; On-site; MXN 350,000 - 520,000; Full time

Job summary

Dünnpharma S.A. De C.V. in León, Guanajuato, seeks a meticulous Ingeniero Químico de Control de Calidad to ensure product integrity and regulatory compliance throughout manufacturing.

You will develop, implement, and oversee QC procedures from raw materials to finished product release, with a strong emphasis on GMP/ICH standards and analytical testing. The ideal candidate holds a Bachelor's in Chemical Engineering, Chemistry or Pharmacy, with at least 3 years in pharma QC/QAS, proficiency in

Qualifications

• Bachelor's degree in Chemical Engineering, Chemistry, Pharmacy, or related field.
• Minimum 3 years in quality control or quality assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and other regulatory requirements.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Experience with laboratory information management systems (LIMS).
• Strong understanding of statistical analysis and data interpretation.
• Excellent attention to detail, accuracy, and documentation skills.
• Good communication and interpersonal skills.
• Ability to work effectively in a team and manage multiple tasks.

Responsibilities

• Develop and validate analytical methods for raw materials, in-process samples, and finished products.
• Perform quality control testing according to protocols and pharmacopeial standards.
• Ensure GMP compliance and participate in audits.
• Investigate deviations and CAPA implementation.
• Maintain detailed records of all quality control activities and results.
• Calibrate and maintain laboratory equipment to ensure accuracy and reliability.
• Collaborate with production and R&D teams to resolve quality-related issues.
• Stay updated on current trends and regulations in pharmaceutical quality control.
• Contribute to continuous improvement of quality systems and processes.

Skills

Quality control

GMP compliance

Analytical testing

Statistical analysis

Documentation

Teamwork

Communication

Education

Bachelor's degree in Chemical Engineering

Bachelor's degree in Chemistry

Bachelor's degree in Pharmacy

Tools

HPLC

GC

UV-Vis spectroscopy

Titration

LIMS

Job description

About the Role

Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Ingeniero Químico de Control de Calidad to ensure the highest standards in their product manufacturing. This role is based in León, Guanajuato, MX , and is crucial for maintaining product integrity and regulatory compliance. You will be responsible for developing, implementing, and overseeing quality control procedures throughout the manufacturing process, from raw material inspection to finished product release. The ideal candidate will have a strong background in chemical engineering or chemistry, extensive knowledge of quality assurance systems (GMP, ISO), and experience with analytical testing methodologies within the pharmaceutical industry. We are looking for a detail-oriented professional committed to upholding product quality and safety.

Key Responsibilities

• Develop and validate analytical methods for raw materials, in-process samples, and finished products.
• Perform quality control testing according to established protocols and pharmacopeial standards.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Investigate deviations and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPA).
• Maintain detailed records of all quality control activities and results.
• Calibrate and maintain laboratory equipment to ensure accuracy and reliability.
• Participate in internal and external audits as a quality control representative.
• Collaborate with production and R&D teams to resolve quality-related issues.
• Stay updated on current trends and regulations in pharmaceutical quality control.
• Contribute to the continuous improvement of quality systems and processes.

Requirements

• Bachelor's degree in Chemical Engineering, Chemistry, Pharmacy, or a related field.
• Minimum of 3 years of experience in quality control or quality assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Experience with laboratory information management systems (LIMS).
• Strong understanding of statistical analysis and data interpretation.
• Excellent attention to detail, accuracy, and documentation skills.
• Good communication and interpersonal skills.
• Ability to work effectively in a team environment and manage multiple tasks.

Benefits

Our client offers a competitive salary, a comprehensive benefits package, and significant opportunities for professional development within the pharmaceutical sector. You will work in a state-of-the-art facility with