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CCP RECRUITMENT - Shift Production Supervisor
Shift Production Supervisor Job Description This position will report to the Process Shift Manager. The successful candidate will be part of the manufacturing shift team. Responsibilities will include maintaining the highest standards of safety and quality within the department. The person selected will work closely with the Process Shift Manager ensuring the smooth operation of the processing department. The main duties will consist of stock control, ingredient allocation, compliance, operator training and ensuring achievement of the production schedule. The successful candidate will have the opportunity to participate as a team member in process projects. The processing area operates 7 days a week 24 hours a day. This role will involve shift work. Skills/Experience Requirements The ideal candidate must have excellent communication skills, as well as analytical and problem solving skills. The successful candidate will work well on his/her own initiative, make sound decisions and have demonstrated ability to work in a team environment. Experience in a food, beverage or pharmaceutical industry with supervisory experience would be an advantage. Good computer skills will be required for this role

1st Pharma People - Senior Vendor Engineer
Key Accountabilities: • Lead a team comprising members from purchasing, supplier quality and business units responsible for all aspects of supplier management for plastics and packaging components. • Develop new supply sources with purchasing team - qualify components to specified parameters. • Contributes to the development, maintenance and improvements of supplier management policies and procedures. • Provides guidance to other functional areas in applying supplier management system requirements • Promoting the Quality System within the Supply Base - working with Purchasing, Supplier Quality Engineering, Receiving Inspection & the Value Streams to ensure that components meet our requirements. • Dealing with component specification/quality issues as they arise - work with quality and supply groups to disposition product. • Ensuring that adequate corrective action is put in place by suppliers and monitor effectiveness of same. • Assist maintenance of Approved Vendor list and Service Providers lists per agreed guidelines for approval. • Support supplier quality rating to a level which allows certification or dock to stock programs to be implemented. • Lead/work on Process Improvement teams relating to component usage or design. • Drive value improvement programmes with suppliers & support validation plans for new & substitute materials/suppliers • Work closely with suppliers globally and to execute Value Engineering/Component Engineering opportunities to take cost out of product. • Communicate any Transitions to all stakeholders and receive buy-in for implementation timeline. • Responsible for achieving business objectives: productivity, defect reduction, lead-time reduction, on-time delivery, and new supplier launches. • Assist in the negotiation process with suppliers by providing specific category technical expertise. Skills, Experience & Qualifications: • Bachelor's degree and minimum 3 years relevant work experience. • You will possess excellent communication skills and be looking for a challenging role. • Demonstrated track record in development of new supply sources will be a distinct advantage. • Project Management skills to manage supplier/material changes within the Company & with the Suppliers. • Six Sigma Black Belt or Green Belt certification is desired. • Lean working knowledge is desired. • Ability to work with minimum supervision. • Excellent interpersonal and communication skills. • Excellent team leadership skills and proven track record of technical leadership in the packaging and plastics supplier management.

1st Pharma People - Senior Quality Engineer-Operations
Key Accountabilities: • Selects appropriate techniques for problem solving and makes solid and consistent Engineering and Quality Assurance recommendations. • Demonstrates and actively promotes highest levels of professional QA engineering discipline. • Viewed as a leader in the areas of QSR and ISO/MDD standards, constantly promote awareness of best industry practices making appropriate decisions on a daily basis using the Quality Engineering Manager/Site QA Director as the final arbitrator on critical quality decisions. • Has significant expertise in validation engineering and is thoroughly familiar with all regulatory requirements. • Champions continuous improvement and innovation from a quality perspective within the department right from vendor selection/approval through to customer awareness/satisfaction. • Is an effective team member, fully motivated to achieve and demonstrate best practices in line with the department and LRP objectives. • Gives technical guidance to Quality Engineers, Associate Quality Engineers, technicians and inspection staff. • Works with EHS to identify significant environmental impacts of operations and to establish goals and targets around significant environmental impacts. Skills, Experience & Qualifications: • A graduate of Engineering, Sciences or equivalent experience with a minimum of 5 years experience in a healthcare environment or other similar environment. • Should be able to deal with suppliers, other engineering disciplines within and outside of Site and customers should the need arise. • People Management experience essential.

1st Pharma People - Instrument Service Engineer
Job Summary: • To service and repair a range of clinical analysers. • To create and maintain the preventive maintenance programme for analysers used for testing Reagent products. • To carry out mandatory updates to clinical analysers • To carry out instrument calibration. • To maintain records for all maintenance and calibration carried out. • Liaise with service engineers and U.S. counterparts to ensure systems are current with test specifications and procedures requirements. Job Function: • Purchases spare parts and maintains adequate stock for clinical analysers. • Liaise with Technical Operations on technical issues associated with instruments and/or the product testing. • Participates in the investigation of root cause analysis on reagent test issues, customer complaints and corrective actions. • Supports the introduction of new products. Provides technical support to laboratory technicians including training in system operation and routine maintenance. • Supports the development of in-house ranges for all chemistries. Maintains related standard operating procedures and supports validation efforts. • Involvement in team activity to support a programme of continuous process improvement. Education/Experience: • Third level qualification in Electronic Engineering or equivalent. • Minimum 3 years relevant experience in an Electronic or Electromechanical manufacturing environment. • Good knowledge of the repair and testing of Diagnostic Instruments and strong analytical and troubleshooting skills to identify problems and take corrective action. • A good knowledge of GMP, ISO/FDA requirements and computer literacy is required. Offer: • Defined benefit pension plan. • 100% health care plan for employee plus immediate family. • Profit share bonus scheme average yields 8.5% of annual salary. • Relocation fund is offered if required.

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