Key Responsibilities
? Execute manufacturing activities according to production plans, including non-routine runs.
? Manufacture validation, clinical, and commercial batch.
? Support ongoing improvement of existing manufacturing processes.
? Perform and support process validation activities.
? Maintain manufacturing documentation (SOPs, work instructions, batch records).
? Support deviation investigations and CAPA activities with QA.
? Monitor raw material and packaging inventory and initiate purchase requests.
? Support warehouse and documentation activities in accordance with ISO 13485.
? Work closely with R D, Engineering, Quality, and Regulatory teams.
Requirements: ? Bachelors degree in engineering (Chemical, Biotechnology, Materials, Industrial Engineering, or related field).
??2-3 years of experience in a Production / Process / Manufacturing Engineering role
? Experience as a Process / Manufacturing Engineer in a medical device company - advantage.
? Experience in process validation, deviation management, and documentation.
? Experience working under ISO 13485 - advantage.
? Experience manufacturing validation, clinical, or commercial batches - advantage.
This position is open to all candidates.