Job Description

Position: Temporary Assignment Production SupervisorIndustry: PharmaceuticalStart Date: September 1, 2023

Duration: Temporary assignment (specific duration to be determined)

Company Overview:Leading pharmaceutical company dedicated to improving global health through the development, manufacturing, and distribution of high-quality pharmaceutical products.

Job Overview: Our client is seeking experienced Production Supervisors to join their team on a temporary assignment basis. Production Supervisors will play a critical role in overseeing and managing production operations, ensuring compliance with industry standards, quality control, and safety regulations. The successful candidate must have a strong background in the pharmaceutical industry, with proven experience in production management and regulatory compliance.

Responsibilities:

• Lead and supervise production teams to ensure efficient and effective manufacturing processes.
• Plan and schedule production activities to meet production targets while optimizing resource utilization.
• Monitor production processes, identify areas for improvement, and implement corrective actions to enhance productivity and quality.
• Ensure strict adherence to GMP (Good Manufacturing Practices) and other relevant regulatory guidelines.
• Collaborate with cross-functional teams, including quality assurance, regulatory affairs, and maintenance, to achieve production goals.
• Conduct regular performance evaluations for production staff, provide feedback, and facilitate training as needed.
• Maintain accurate production records, batch documentation, and other necessary documentation.
• Identify and troubleshoot production issues, implementing solutions to minimize downtime and prevent future occurrences.
• Implement safety protocols and promote a culture of safety awareness among production staff.
• Support continuous improvement initiatives, driving operational efficiency and cost-effectiveness.

Qualifications:.

• Minimum of 1 years of experience in pharmaceutical production, with at least 1 years in a supervisory role.
• In-depth knowledge of GMP regulations, and other relevant pharmaceutical industry standards.
• Strong leadership and team management skills, with the ability to motivate and inspire production teams.
• Excellent problem-solving abilities and a proactive approach to identifying and resolving operational challenges.
• Effective communication skills, both written and verbal, to interact with various teams and stakeholders.
• Proficiency in using production management software and tools.
• Ability to work in a fast-paced environment, manage priorities, and adapt to changing circumstances.
• Attention to detail and a commitment to maintaining the highest standards of product quality.

Application Process:Interested candidates are requested to submit their updated resume along with a cover letter highlighting their relevant experience in the pharmaceutical industry. Shortlisted candidates will be contacted for further assessments and interviews.

Note: This is a temporary assignment with a specific duration. Compensation and benefits will be discussed during the interview process.

Application Deadline: 23rd August 2023

This job specification is intended to convey information essential to understanding the scope of the position and the general nature and level of work performed. It is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities, or working conditions associated with the position.

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