Production Support Specialist

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 optimize the health, wellbeing and productivity of the world’s animals. 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 commercialization 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.

**About the role**:
Reporting to the Plant Manager, the primary role and tasks for the Production Support Specialist Level 1 is to perform and coordinate all aspects of investigations of production/manufacturing related incidents and deviations to ensure compliance with pharmaceutical products manufacturing and cGMP. A detailed oriented individual will conduct root cause investigations, close deviations on time, support assignment of proper corrective actions, and facilitate the implementation of corrective actions for manufacturing and operating processes. Using a hands-on approach, the specialist actively executes the deviation investigations, effective and efficient investigation writing, corrective and preventive actions development & implementation with production and supporting stakeholders. The Specialist will work closely with all in compliance with current FDA and Health Canada regulations, cGMP and GDP practices. Participation in Regulatory Agency inspections/activities required as needed.

**What you'll do**:
**Deviation Investigations & Writing**
- Work hands on with production and quality, on the manufacturing floor to collect and collate all required information, data and facts at the point of issue and deviation occurrence.
- Meet and exceed performance and deliverable expectations of completing investigations and writing investigations on time as laid out by the plant manager.
- Review batch documentation, testing results, training records, calibration records, policies, standard operating procedures, regulatory policies, testing and manufacturing specifications, validation documents, and other technical documents to support the deviation investigations and writing.
- Lead the investigation closure of manufacturing compliance-related documents using quality and statistical tools to identify and implement proper corrective and preventative actions to manufacturing non-compliance on time.
- Write deviations investigations using the right writing and compliance practices. Writing should be SMART - Specific & Situational, Measurable & Methodical, Actionable & Accurate, Realistic and Timely.

**Continuous Improvement**
- Engages and performs deviation investigations process by understanding the current state of process, sequence of flow, breaking down the problem into what, where, when, who, how: determines the point of cause, analyses and determines the real root causes by using various problem solving tools - Cause and Effect, 6M -Fishbone Analysis, 5 Whys, Pareto and Graphical Analysis, Process Capability Methods; and Right Countermeasure Development.
- Use A3-8 Step problem solving methodologies to facilitate investigations. Work with production and supportive stakeholders to determine possible countermeasures for CAPAs.

**Training**
- Deliver training programs designed to enable staff to consistently execute all manufacturing processes with strict compliance to cGMPs, EHS regulations and any other CAPA improvements related training.
- Identify and implement process improvements to drive success in the areas of quality, compliance, throughput flow, workplace safety, cost-effectiveness, and product lead time through CAPAs
- Keep current with new guidelines and Health Canada and FDA inspectional and scientific trends; and adjust CAPA procedures appropriately.
- Work with management team to improve the quality of the process and the procedures.
- Any other tasks and duties as assigned

**What you bring to the role**:
**Essential**:

- Prior experience in an aseptic manufacturing environment required;
- Training and knowledge of Good Manufacturing Practice regulations and standards;
- Bachelor’s Degree in Life Sciences Microbiology or equivalent degree/diploma required
- Direct knowledge of cGMP regulations;
- Able to develop, review and maintain metrics and quality audits;
- Ability to prioritize and manage multiple tasks to demanding deadlines;
- Able to interface directly with cross-functional teams;
- High level of personal motivation;
- Extremely detailed oriented and analytical thinker with strong problem-solving ability;
- Excellent written and verbal co