Permanent Manufacturing Jobs in Falkirk

3 of 3 Permanent Manufacturing Jobs in Falkirk

Graduate Sales & Business Development Executive

G68, Banknock, Falkirk, Stirling and Falkirk, United Kingdom
DPS Group
literate – proficiency with Microsoft Office packages. Have a passion for digital transformation. Excellent communication skills, both written and verbal. Full UK Driving Licence. DPS – Who Are We? We solve manufacturing challenges through the intelligent use of technology. DPS Group is one of the UK’s leading integrated electrical, instrumental & control and compliance providers. We are trusted to deliver integrated solutions More ❯
Employment Type: Permanent
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Business Development Manager

Falkirk, Stirlingshire, United Kingdom
Hybrid / WFH Options
Wallace Hind Selection LTD
Manager, Technical Sales Manager - Plant Hire, Plant Sales, Equipment Rental, Specialist Machinery, Conveyors, Cement & Concrete, Timber, Steel & Foundry, Bulk & Minerals, Energy & Power, Building Materials, Pulp & Paper, Quarrying, & Aggregates, Asphalt Manufacturing, Power Stations, Grain Processing, Shotblasting, Insulation Manufacturing. INTERESTED? Please click apply. You will receive an acknowledgement of your application. Wallace Hind Selection, alongside our client embrace diversity, champion equality, and More ❯
Employment Type: Permanent
Salary: GBP 40,000 - 45,000 Annual
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Quality Assurance Officer (Pharma)

Grangemouth, Scotland, United Kingdom
Piramal Pharma Solutions
our QA department in Grangemouth. The Quality Assurance officer will act as the Quality Assurance representative for campaign projects, ensuring accuracy and compliance of procedures, quality management system records, manufacturing batch records and associated testing. Be the QA representative for new products and for change projects, dealing with aspects including review/approval of process instructions, change controls, deviations, investigations … internal and external stakeholders to ensure quality of all product related activities. Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures, Analytical Procedures and associated documentation. Participate in quality related investigations, assist in the development, approval and implementation of effective CAPA in order to resolve production, audit and customer issues. … Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical/production/packaging equipment and cleaning procedures Participate in the audits of suppliers and self-inspection of internal production and support functions as required Be involved in preparation for and successful completion of MHRA/FDA and other regulatory body audits. Coordinate quality More ❯
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