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Vice President- Plant Operation

Experience: Min 10 Years

Qualification: Master Degree in Pharmacy (M. Pharm) and an MBA.

Key Responsibilities:

Strategic Leadership:

Develop and execute operational strategies that align with corporate goals, focusing on efficiency, quality, and innovation in LVP and SVP production.

Lead initiatives to enhance manufacturing processes, adapting to market changes and technological advancements.

Regulatory Compliance:

Ensure adherence to DDA regulations, GMP standards, and other relevant industry guidelines governing LVP and SVP manufacturing.

Manage the preparation and execution of regulatory inspections, audits, and submissions.

Operational Management:

Oversee day-to-day operations of the manufacturing facility, including production planning, scheduling, and resource allocation.

Optimize manufacturing workflows to improve productivity, reduce waste, and maintain high-quality standards.

Quality Assurance and Control:

Implement and manage comprehensive QA and QC systems to ensure product safety and efficacy.

Collaborate with QC teams to establish and monitor quality metrics, leading investigations into any deviations or non-conformances.

Budgeting and Financial Management:

Develop and oversee the plant’s operating budget, ensuring financial objectives are met.

Conduct cost analyses and implement cost-reduction strategies while ensuring compliance and product quality.

Cross-Functional Collaboration:

Partner with R&D, supply chain, and regulatory teams to facilitate seamless integration of product development and manufacturing processes.

Participate in product lifecycle management, supporting the introduction of new products.

Talent Development:
Mentor and develop plant leadership and operational staff, fostering a culture of performance and quality.

Identify training needs and promote continuous development within the QA and QC teams.

Safety Management:

Champion safety initiatives to ensure a safe working environment for all employees.

Conduct regular safety audits and ensure compliance with health and safety regulations.

Key Requirements:

Master’s degree in Pharmacy (M.Pharm) and an MBA.

Minimum of 10 years of experience in pharmaceutical manufacturing, particularly in LVP and SVP, with at least 7 years in a leadership role.

Strong background in Quality Control and Quality Assurance within the pharmaceutical industry.

Comprehensive knowledge of regulatory requirements and quality management systems.

Proven ability to drive operational improvements and manage complex projects effectively.

Excellent analytical, problem-solving, and decision-making skills.

Strong communication and interpersonal skills, with the ability to influence stakeholders at all levels.

How to apply:

ODI Nepal invites deserving and qualified candidates to submit their updated resume and cover letter, clearly specifying the position being applied for and including both current and expected remuneration. Please send your

application to: vacancy@odinepal.com or vacancyatodinepal@gmail.com at your earliest convenience.

Apply before: October 31, 2024 12:00 am

Company Name: Everest Parenterals Pvt. Ltd. , Factory at Chhatapipra, Bara, Simara

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