Deputy Manager Production Manufacturing

Unichem Laboratories Ltd.; Ghaziabad District; In loco; INR 600.000 - 900.000; Tempo pieno

Descrizione del lavoro

Unichem Laboratories Ltd. in Ghaziabad, India is seeking a production supervisor to oversee the manufacturing department, ensuring efficient operations and adherence to production schedules.

You will coordinate with QA for self-inspections, manage SOPs, batch documentation, and training of personnel, while fostering teamwork and resolving issues with Quality Management. Experience in pharmaceutical manufacturing, especially Oral Solid Dosage forms, with regulatory exposure to USFDA, MHRA, EU,

Competenze

• Experience in the pharmaceutical industry, preferably in Oral Solid Formulations, with regulatory exposure to USFDA, MHRA, EU, TGA, etc.
• Leadership, teamwork, problem-solving, analytical thinking, and excellent verbal and written communication skills.

Mansioni

• Ensure the efficient functioning of the production department.
• Ensure the maintenance of production equipment and coordinate its installation and qualification.
• Ensure the timely preparation, initiation, and review of departmental SOPs.
• Ensure the timely closure of change controls and deviations.
• Provide necessary training to production department personnel on an ongoing basis.
• Ensure the timely completion of batch documents, such as MPCR-I and MPCR-II.
• Supervise production operations effectively and efficiently.
• Coordinate with QA for self-inspections and ensure compliance with audit observations.
• Foster a collaborative team environment within the department and resolve all issues in coordination with Quality Management.
• Coordinate with the warehouse for material issuance and ensure adherence to the production schedule.
• Ensure adherence to good documentation practices and maintain accurate, contemporaneous records.

Conoscenze

Pharma industry experience

Leadership & communication

Descrizione del lavoro

Responsibilities

• Ensure the efficient functioning of the production department.
• Ensure the maintenance of production equipment and coordinate its installation and qualification.
• Ensure the timely preparation, initiation, and review of departmental SOPs.
• Ensure the timely closure of change controls and deviations.
• Provide necessary training to production department personnel on an ongoing basis.
• Ensure the timely completion of batch documents, such as MPCR-I and MPCR-II.
• Supervise production operations effectively and efficiently.
• Coordinate with QA for self-inspections and ensure compliance with audit observations.
• Foster a collaborative team environment within the department and resolve all issues in coordination with Quality Management.
• Coordinate with the warehouse for material issuance and ensure adherence to the production schedule.
• Ensure adherence to good documentation practices and maintain accurate, contemporaneous records.

SKILLS

• The candidate should have relevant experience in the pharmaceutical industry, preferably in Oral Solid Formulations, with regulatory exposure to USFDA, MHRA, EU, TGA, etc.
• The candidate should demonstrate leadership, teamwork, problem-solving ability, analytical thinking, and excellent verbal and written communication skills.