Pharmaceutical Production Supervisor Job Vacancy in Xai-Xai, Mozambique – Pharmaceutical Manufacturing

Job Description

Position: Pharmaceutical Production Supervisor

Company: Novartis

Location: Xai-Xai, Mozambique

Experience: 5+ years in pharmaceutical manufacturing

Education: Bachelor’s degree in Pharmacy, Chemical Engineering or related field

Employment Type: Full-time

Industry: Pharmaceutical Manufacturing

Department: Production

Salary: 800,000 – 1,200,000 SSP per month

Vacancies:1

Company Overview

Novartis is a global leader in innovative medicines, vaccines, and consumer health products, operating in more than 150 countries worldwide. In Mozambique, Novartis has established a strong presence through partnerships with local distributors, government health programs, and research institutions. The company is committed to improving health outcomes, fostering sustainable development, and investing in local talent. By leveraging cutting‑edge technology and a robust quality management system, Novartis delivers high‑quality pharmaceutical products that meet stringent international standards. The Xai‑Xai production hub plays a strategic role in serving the southern region of Mozambique, supporting both domestic demand and regional export initiatives. This environment offers a dynamic platform for professionals seeking to contribute to life‑saving medicines while advancing their careers in a globally recognized organization. Mozambique Jobs, Jobs in Mozambique, and Career Opportunities in Mozambique are integral to Novartis’ growth strategy, emphasizing local employment and skill development.

Job Overview

The Pharmaceutical Production Supervisor will lead a team of operators and technicians in the manufacturing of solid oral dosage forms, ensuring compliance with Good Manufacturing Practices (GMP), safety regulations, and production targets. This role is pivotal in maintaining product quality, optimizing process efficiency, and driving continuous improvement initiatives. The supervisor will coordinate with quality assurance, engineering, and supply chain departments to guarantee seamless operations. As part of a forward‑thinking organization, you will have access to state‑of‑the‑art equipment, robust training programs, and a collaborative culture that values innovation. For more information about our global career portal, visit https://mozambiquejobsearch.com.

Explore related opportunities in neighboring markets at https://malawijobsearch.com/job-vacancy-in-malawi/.

Additional regional insights are available at https://zimbabwejobsearch.com/.

Key Responsibilities

• Supervise daily production activities for tablet and capsule lines, ensuring adherence to batch records and SOPs.
• Monitor critical process parameters, troubleshoot deviations, and implement corrective actions promptly.
• Coordinate with Quality Assurance to conduct in‑process testing, release decisions, and investigations of non‑conformances.
• Lead shift handovers, communicate production status, and update management on key performance indicators.
• Drive continuous improvement projects using Lean Six Sigma methodologies to enhance yield, reduce waste, and improve cycle times.
• Ensure compliance with health, safety, and environmental regulations, conducting regular safety briefings and audits.
• Maintain equipment logs, schedule preventive maintenance, and liaise with Engineering for equipment qualification.
• Develop and mentor production staff, providing coaching, performance feedback, and career development plans.

Required Skills

• Strong knowledge of GMP, FDA, and WHO pharmaceutical manufacturing standards.
• Proficiency in batch record review, deviation management, and change control processes.
• Excellent leadership and team‑building abilities with a focus on safety culture.
• Analytical mindset with capability to interpret process data and drive data‑based decisions.
• Effective communication skills in English and Portuguese, both written and verbal.
• Experience with ERP systems such as SAP or Oracle for production planning.
• Problem‑solving aptitude and ability to work under pressure to meet tight deadlines.

Education

A Bachelor’s degree in Pharmacy, Chemical Engineering, Pharmaceutical Sciences, or a related discipline is required. Advanced certifications in GMP, Lean Six Sigma, or Production Management are considered an advantage.

Experience

Minimum of five years of hands‑on experience in pharmaceutical manufacturing, with at least two years in a supervisory or lead role. Experience in solid dosage form production is highly preferred.

Salary

The position offers a competitive salary ranging from 800,000 to 1,200,000 SSP per month, commensurate with experience and qualifications. Performance‑based bonuses and annual salary reviews are part of the compensation package.

Benefits

• Comprehensive health insurance covering employee and dependents.
• Retirement savings plan with company matching contributions.
• Paid annual leave, sick leave, and public holidays.
• Transportation allowance for commuting to the Xai‑Xai facility.
• Employee assistance program and wellness initiatives.

Training

• On‑boarding program covering GMP, safety, and company policies.
• Continuous professional development through internal workshops and external certifications.
• Leadership development tracks for high‑potential supervisors.

Working Environment

The Xai‑Xai production site is a modern, climate‑controlled facility equipped with advanced manufacturing lines, clean rooms, and robust quality control laboratories. The workplace promotes a culture of safety, collaboration, and innovation, encouraging employees to share ideas and contribute to process enhancements. Flexible shift patterns are available to support work‑life balance while meeting production demands.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining relevant experience through the Novartis careers portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be contacted for a virtual interview followed by an on‑site assessment. Please ensure all documents are in PDF format and clearly indicate the job title in the subject line.

Equal Opportunity Statement

Novartis is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, regardless of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic. Employment decisions are based solely on qualifications, merit, and business needs.