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Please Note: These job postings require all applicants to speak fluent spanish, and live in Santo Domingo, Dominican Republic.

 

Quality Assurance Manager

Responsibilities:

  • Develop and implement the quality assurance system.
  • Monitor compliance with BPMs.
  • Manage the quality assurance team.
  • Analyze quality control data and report results.
  • Manage quality deviations and corrective actions.
  • Collaborate with other departments to ensure product quality.
  • Maintain updated documentation.
  • Manage and implement changes and improvements.

Requirements:

  • Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, or related fields.
  • Minimum 2 years of experience in quality assurance in the pharmaceutical industry, with experience in team management.
  • Thorough knowledge of Good Manufacturing
  • Practices (BPM), ISO 9001:2008, laboratory equipment, and software management (Windows, Word, Excel, etc.).
  • Leadership skills, effective communication, project management, data analysis, problem-solving, and decision-making.
  • Knowledge of quality tools (charts, FMEA, Balanced Scorecard, among others).

Apply for this position by entering your email address and attaching your resume:

 

Pharmaceutical Production Manager

Responsibilities:

  • Supervise and coordinate pharmaceutical production processes, ensuring quality and efficiency.
  • Carry out the entire drug manufacturing process according to GMP, GPD, and GLP standards.
  • Formulate and reformulate weighing controls for manufacturing.
  • Manage production equipment, verifying the different areas and machinery.
  • Monitor the inventory of raw materials and finished products, ensuring proper production flow.
  • Prepare and document periodic reports on production area performance, process forms, and records of manufactured batches.
  • Supervise the work of the Production staff under their supervision during the manufacturing process.

Requirements:

  • University degree in Pharmacy.
  • Minimum of 1 year of experience in the pharmaceutical industry, preferably in production areas.
  • Knowledge of BPM and BPL regulations, and ISO 9001-2008 standards.
  • Knowledge of production machinery.
  • Proficiency in computer software (Windows, Word, Excel, Project Management, etc.).
  • Leadership and teamwork skills.

 

Apply for this position by entering your email address and attaching your resume:

 

Note: All other responsibilities and requirements will be specified during the interview.

 

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