Role Specific Requirements:
- Conduct incoming inspections of labeling materials and packaging components.
- Perform initial inspection of the packaging lines to ensure compliance to company Standard Operating Procedures.
- Review equipment cleaning and usage logs.
- Write, review, and revise Standard Operating Procedures.
- Support Continuous Improvement program throughout the company.
- Review batch documentation for GMP Compliance. .
- Conducts the annual inspection of retained samples and investigates any discrepancies.
- Interface with FDA compliance officers during facility inspections.
- Performs final reconciliation of raw materials and finished packaged products to ensure all material is accounted for within established limits.
- Prepares raw materials and finished product samples for submission to the Quality Control laboratory. Releases acceptable lots.
Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve.
Essential Requirements:
- Practical experience with GMPs within a regulated environment.
- High school diploma or equivalent.
- Strong problem identification and problem resolution skills.
- High level of proficiency with Microsoft Office.
- Excellent written and verbal communication skills.
- Physical ability to maneuver 100 pound roll stock rolls.
- Ability to bend, squat, and lift 25 pounds.
- Highly motivated and self-directed capable of multi-tasking, and able to work with minimal supervision.
- Extremely detail-oriented and analytical thinker.
- Strong work ethic and positive team attitude.
Desirable Requirements:
- Experience in an FDA, Canadian Health, and or EU regulated pharma manufacturing environment.
- Minimum 6 months of experience in pharma or food manufacturing or Quality Assurance.
- Bachelor’s Degree.
- Experience and knowledge with Continuous Improvement programs.
Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve.
Bimeda is a leading global innovator, manufacturer and marketer of veterinary pharmaceuticals and animal health products and has over half a century’s experience in providing science-driven solutions to optimise the health, wellbeing and productivity of the world’s animals.
Bimeda’s global innovation programme sees six state-of-the art R&D centres across four continents collaborate on an enviable product development pipeline which anticipates the ever-evolving needs of the animal health industry.
Bimeda’s nine manufacturing facilities across seven countries allow the company to manufacture a broad range of preventative, curative and nutritional products including sterile injectables, vaccinations, nutritional boluses, feed additives, tablets, water-soluble powders, pastes and non-sterile liquids.
Globally, the company focuses on the development, manufacture and commercialisation of quality Bimeda-branded products while also being the partner of choice for contract manufacturing and R&D services for prominent companies within the animal health industry.
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