Production / Warehouse

Catalent are currently recruiting for a Quality Specialist II to join the Bathgate site. The Quality Specialist will carry out functions relevant to the Quality (GMP) objectives and policies of Catalent. This role will see you join the dedicated and Quality function that are an integral part of our success here at Catalent. In this role you will be responsible for the movement, control and tracking of documentation to adhere to the production schedule. The Role: To be responsible for the movement, control and tracking of documentation, ensuring a timely flow to adhere to the production schedule. Review and approve Material Specifications to ensure compliance with pharmacopoeia and client requirements. To review and approve Incoming Bulk, Intermediate and Finished Materials to ensure compliance with pharmacopoeia and client requirements Review and approve Randomisations to ensure compliance with GMP and client requirements Review and approve GMP information to ensure accuracy

Primary duty is to diagnose complex electronic assemblies down to component level on failing products and recommend appropriate corrective actions. Perform functional testing of electronic assemblies to required contractual, quality and schedule requirements. Diagnose test equipment related faults. Execution of preventative maintenance and calibration plans for test equipment. Record accurate test records and provide requested yield & failure reports. Assist engineering with any ongoing investigations / initiatives. Aid the continual improvement of efficiency in designated test area(s)

Pro-actively managing Health & Safety Leading and driving standards of quality, food safety, hygiene and housekeeping within your area through Good Manufacturing Practice (G.M.P.) Managing performance of your teams Owning the training & development of all levels of team including managers. Managing the NPD process within your area Challenging and introducing new KPIs to drive performance. Planning, organising and measuring labour and material requirements Managing the communication process to ensure that the workforce in their area is well informed on relevant business news Supporting and encouraging the Bakkavör values and a positive culture within your area, whilst fostering good employee relations The recruitment of direct reports and an involvement in all staff recruitment within your area

Your duties as a Picker Packer will include ensuring customer orders are accurately fulfilled and are packed to a high standard prior to shipment. Combined with: Using warehouse machinery to move goods from storage areas to packaging areas Inspecting goods for damage or faults prior to shipment Loading packaged goods into containers for shipping Completing paperwork or entering data into tracking software Ensuring that storage areas are kept fully stocked at all times Following H&S policies and procedures Other general production and warehouse duties

As a Quality Control Operative, you'll ensure that production standards are met and maintained for all goods. Performing checks on random samples from a production line to ensure all products, labelling and packaging meets customer specifications. Other duties and responsibilities include: Conducting quality inspections, assessing quality and ensuring compliance to customer and product specifications Recording results and allocate according to the customer requirements Labelling and packaging checks to ensure accuracy and compliance Producing detailed reports on quality issues found, and communicating to managers Calibrating production equipment

Key Responsibilities: As a Process Engineer, you will: Support the development of a new manufacturing site. Identify and implement strategies to optimise production processes and reduce costs. Plan, execute, and analyse experiments, reporting results effectively. Collaborate with external design and engineering firms. Assist in developing process designs and optimising selected designs. Lead projects related to production scale-up and process improvements. Address plant issues and coordinate solutions. Supervise and mentor team members. Promote a safe, hygienic working environment, adhering to health, safety, and food quality standards.

Build, maintain and motivate a team capable of efficiently setting up Client studies to ensure effective operational execution meeting the Client needs for study design in scope to the contract. Build a team who can manage achieving all documentation and technical targets and training requirements to service customers on time and right first time. Manage work allocation, planning of all tasks proactively, managing the plan, making independent leadership decisions to mitigate risks daily to ensure successful delivery Resource Plan, using data, and S&OP data to ensure resource requirements are met, and constraints identified Mentor, train and coach staff in establishing effective studies with appropriate risk management Work directly with Quality Assurance, Engineering, and Project Management functional areas to plan and implement documentation and training requirements for GMP (Good Manufacturing Practice) activities in manufacturing for clinical packaging operations.

Day shift: 07:00 to 19:00 @ £12 per hour OR Night shift: 19:00 to 07:00 @ £12.60 per hour

Picking and packing products Conducting quality checks Keeping your work area clean and tidy Storing items within the warehouse reporting any issues to your supervisor Meeting production targets to company standard General production and warehouse duties