Biotechnology

Supplier Quality Engineer, Europe (Regulated Industry) - GO/DJS/12631

Hamilton, Scotland | SALARY: Negotiable | Permanent

The Company:

Our client is firmly established as the market leader within their chosen field. Their products comprise of cutting edge medical device technologies used for the purpose of saving lives throughout the world. With operations in sixteen countries spanning three continents our client truly is a global player.

Their reputation for meeting their clients’ needs whilst delivering quality, safety and reliability is unrivalled. With a definite focus on developing their own people they value honesty and transparency within their organisation.


The Role:

An exciting opportunity has arisen for an experienced Supplier Quality Engineer to join their Quality Division.
The overall purpose of this role is quality support European Supplier and contract manufacturing programs.

Selected Key Responsibilities to Include:

• Inolvlement in Supplier Development Programs to include; Supplier Selection and Assessment, Supplier Performance Management, Procurement Specifications, Supplier Quality Issues Management and Approved Supplier List Management.
• Management of the Supplier Audit program.
• Ensure Supplier and Subcontract Manufacturer compliance to Quality Systems, standards and regulations through a process of monitoring (audit) and training.
• Ownership of the corporate Approved Supplier List, working with Supply Chain to add new suppliers and monitor existing suppliers.
• Development of effective assessment tools for supplier selection and supplier performance monitoring
• Support the development of a standardized Quality Management System structure for Europe.
• Provide audit support to the European Internal Audit Program
• Define key processes, process documentation and key performance indicators in conjunction with the process owners for the following areas: Supplier Selection, Approval and Management, European Logistics, European Distribution Centre activities, Returned Goods Activities, European Contract Manufacturing


The Candidate:

• Candidates will be degree qualified (or equivalent) in and Engineering or Quality discipline.

• Experience of working within a Supplier Quality role in the Medical Device industry is required (with knowledge of ISO 13485, 21CFR800, Medical Device Directive 93/42/EEC).

• Candidates with experience gained within highly regulated indsutries where similar regulations, standards or methods exist may be considered (i.e. cleanroom protocols, GMP, FDA regulated, etc).

• Experience of conducting external supplier/subcontractor audits is required. Lead auditor qualification would represent a distinct advantage. Experience within a similar role in a GMP regulated environment is required (i.e. medical device/ pharmaceutical/ food).

• Candidates must be willing to travel regularly within Europe (up to 25% time spent travelling).


Apply:

Apply today and work for a highly successful, market leading company whose products change and often save people’s lives.
Contact Dan Stewart on 01506 461445, email your CV to dan.stewart@go-escape.com or Send this job to a friend

Product Development Manager (Chemicals) - GO/DJS/12621

Glenrothes, Scotland | SALARY: Negotiable | Permanent

THE COMPANY:

Our client is a leading global manufacturer of chemicals with a presence across 3 continents. From their base near Glenrothes, they supply high quality products to a varied customer base.


THE ROLE:

Due to continued growth at their facility in Fife, they are looking for an experienced Product Development Manager. The overall purpose of this role is to develop new and existing products whilst managing laboratory staff.

Key Responsibilities to include:

• To develop new innovative products within the framework of ISO 14001/9001
• To meet customer requirements both in the development of new and existing products or the development of alternatives to a competitor product
• To manage pilot plant activities and the sampling department
• To run production trials on developed materials
• To deliver process improvements
• To develop and maintain a system of evaluation of new raw materials
• To evaluate laboratory equipment and suggest improvements
• To develop a team that is highly responsive to customer demands including an understanding of our commitment to customer satisfaction


THE CANDIDATE:

• Degree qualified (or equivalent) in a science discipline (preferably Chemistry)
• Proven track record in Product Development (formulating new products within chemicals / similar industry such as coatings, paints, plastics, pigments, etc – process methods may involve the likes of blending, milling, mixing or similar)
• ISO/quality experience
• Management/supervisory experience
Contact Dan Stewart on 01506 461445, email your CV to dan.stewart@go-escape.com or Send this job to a friend

Physical & Analytical Chemistry Manager - GO/MJ/12663

Edinburgh, Scotland | SALARY: Negotiable | Permanent

Physical & Analytical Chemistry Manager

My client is seeking a Manager to lead the Respiratory Technology team at their main facility. The successful candidate will supervise and co-ordinate the activities of up to 4 teams of Scientists & Technicians. These activities will include the conduct of analyses and data reporting in accordance with the requirements of project contracts and/or technical agreements assigned to the Analytical Chemistry Department.

The key responsibilities of this role are:

• To plan, prioritise, organise and execute the conduct of analytical work in accordance with the requirements of the client contract and/or technical agreement.
• To assist in production of costing and time lines for client projects.
• To maintain project time lines and budget, manage group capacity, and report revenue forecasts on a monthly basis.
• To assure the integrity and quality of analytical data produced by ensuring staff are adhering to all relevant in-house and client SOPs and methodologies and following the requirements of GMP and GLP.
• To ensure that safe working practices are adopted in the laboratory and to comply with in-house SOPs and other safety legislation (e.g. COSHH).
• To communicate effectively with both internal and external customers, peers and supervising managers to facilitate the smooth conduct of project activities.
• To establish and maintain technical communications with other corporate groups.
• To maintain awareness of modern techniques and their application to Pharmaceutical Sciences activities.

The ideal candidate will have a proven record in managing/supervising a team and have experience of working with external clients. A working knowledge of inhalation product development and analysis is desirable as is experience of working within a GMP regulated environment. Candidates will also have excellent communication skills, a proactive approach to problem solving and the ability to manage conflicting and changing priorities. The individual is required to be well organised, customer focused and a strong team, player.

If you have the relevant skills for this position please forward an up to date CV to moses.jow@go-escape.com or call me on 0141 410 9121.

Contact Moses Jow on 0141 410 9121, email your CV to moses.jow@go-escape.com or Send this job to a friend