PRODUCTION & SUPERVISOR

Description

We are HIRING

PRODUCTION & SUPERVISOR

Location: Nairambi, Kenya

As a production supervisor, you will play a critical role in supporting the Head of Production, Pharmacist and wider production team in the preparation, manufacturing, and packaging of sterile products. You will be responsible for supervising daily-to-day manufacturing tasks in compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and regulatory requirements. You will be heavily involved in the preparation of production documents and work environments, and the quality of finished products and equipment. This hands-on role requires knowledge of GMP, ensuring quality, safety, and compliance, planning, and teamwork.

Key Responsibilities
- supervise sterile manufacturing operations, including batch processing, equipment setup, and line clearance activities
- oversee the preparation, cleaning, and sterilization of manufacturing equipment, tools, and consumables in line with validated procedures.
- supervise windowing, dispensing, and staging of raw materials, components, and consumables in compliance with GMP standards.
- monitor and maintain inventory of materials and consumables within the production arena; ensure cleanroom standards are upheld.
- accurately record complete production documentation including batch records, logbooks, equipment logs, and cleaning records.
- oversee warehouse operations including receipt, storage, issuance, and documentation of materials as per GMP and SOP requirements.
- ensure reusable records - records such as batch card, material issuance logs, and delivery notes - are updated accurately and promptly.
- support the Production Pharmacist in troubleshooting and resolving operational issues and deviations.
- actively participate in training sessions, continuing improvement initiatives, and regular team meetings to drive quality and efficiency.

Qualifications
- Diploma or equivalent in Pharmaceutical Science, manufacturing, or related field (or equivalent industry experience).
- minimum of 2 years of GMP participation / experience / training in manufacturing or a related field.
- Strong communication skills and ability to follow detailed instructions.
- reliable, organized, and able to work within a highly regulated environment.

Desirable Skills
- Experience working in a GMP pharmaceutical production facility (or similar non-sterile).
- Basic knowledge of OPCs and batch record completion and GMP documents
- GxP knowledge

Why Join Us?
At Tasa Pharma, you will gain hands-on experience in a high-class pharmaceutical manufacturing environment. We offer training and development opportunities to grow within production and quality functions. You will work under a supportive team with a focus to deliver operational excellence and contribute to the delivery of essential medicines for Kenya.

Send applications to info@taspaharma.com
Deadline: COB 4th August 2023
Successful candidates will be called for interview.