Senior Production Manager

hace 4 semanas


Xico, México Dr. Reddy'S Laboratories Ltd A tiempo completo
{"title": "Production Operations Lead", "content": "Job Description

At Dr. Reddy's Laboratories Ltd., we are seeking a highly skilled Production Operations Lead to join our Global Manufacturing Organisation (GMO). This role will be responsible for overseeing the production operations of our injectable and oral solid dosage forms (OSDF) departments, ensuring compliance with current Good Manufacturing Practices (cGMP) and regulatory requirements.

Key Responsibilities:
  • Plan, allocate tasks, and supervise production personnel to ensure efficient production operations.
  • Coordinate with various departments, including Research and Development, Quality Assurance, and Engineering, to ensure seamless collaboration and alignment of activities.
  • Identify and address production-related issues promptly, initiate corrective and preventive actions, and facilitate investigations and CAPA closure to minimize disruptions and improve processes.
  • Ensure timely completion of calibration, preventive maintenance, production planning, and other operational activities.
  • Monitor and control the production environment, including temperature, humidity, and cleanliness, to ensure compliance with regulatory requirements.
  • Develop and implement process improvements to increase efficiency, reduce costs, and enhance product quality.
  • Collaborate with the Quality Assurance team to ensure compliance with regulatory requirements and industry standards.
  • Participate in self-inspection audits and provide support to the site investigation team as needed.
Requirements:
  • Master's degree in a relevant field, such as Pharmacy or a related discipline.
  • Minimum 8-12 years of experience in a production operations or quality assurance role in the pharmaceutical industry.
  • Strong leadership and communication skills, with the ability to motivate and guide a team.
  • Excellent problem-solving and analytical skills, with the ability to identify and address complex issues.
  • Knowledge of cGMP and regulatory requirements, with the ability to ensure compliance.
  • Ability to work in a fast-paced environment, with multiple priorities and deadlines.
What We Offer:
  • A competitive salary and benefits package.
  • Opportunities for career growth and professional development.
  • A dynamic and supportive work environment.
  • Recognition and rewards for outstanding performance.

We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and experienced professional looking for a new challenge, please submit your application, including your resume and a cover letter, to [insert contact information].

", "lang_code": "en-US"}

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