Manufacturing Chemist

Job Summary
We are currently recruiting for this position
Minimum Qualification:
OND
Experience Level:
Mid level
Experience Length:
5 years
Job Description
Essential Job Requirements
OND/B.Sc in Pharm tech, chemistry or related field
Minimum of 5 years working experience
Good communication skills
Meticulous attention to details
Critical thinker and problem-solving skills
Integrity and diligence to work
Computer literate
Ethical and highly coordinated
Experience in cGMP manufacturing
Excellent written and oral communication skills and ability to maintain good housekeeping
Flexibility of working hours based on business needs, may include some nights and occasional weekends
Detail-oriented with the ability to troubleshoot and resolve problems
Working knowledge, and progressive understanding of pharmaceutical raw material and production processes
Ability to communicate in a proactive and solution-focused manner, including keeping direct supervisor aware of potential issues
Job Description
Supervise workers during production activities to ensure compliance of laid down structures and guidelines for expected output
Interface with established authority, maintenance team, QA and warehouse personnel
Investigate causes of process failures and develop new procedures for problem-solving to produce a high-quality product and maximize output.
Worked independently performing troubleshooting, staff mentoring, and object-oriented research and analysis.
Ensure full-time compliance to cGMP and safety procedures before, during and after production
Developing relevant SOP’s and methods for production processes and checks
Maintain standard operation procedures to ensure compliance with cGMP.
Perform routine duties on bulk & in-process materials and finished goods.
Filling and recording checklists and logs pertaining to production
Contribute to the efficient production, transfer and release of products from start to finish.
Participate in cross-training with the warehouse, maintenance and QA departments.
Conduct investigations on questionable/problematic batches and document findings.
Follow detailed manufacturing instructions and SOPs to complete assigned production activities according to quality standards
Document and maintain records and notebooks in a neat, thorough, and accurate manner