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Rekrutacje prowadzone przez firmę:
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Recruitment Consultant
Lublin
Wygasła: 21.12.2023
full-time
umowa o pracę
kontrakt B2B
full office work
hybrid work
specialist (Mid / Regular)
Obowiązki:
As a Recruiter , you will: Identify Top Talent: Utilize diverse channels to source and engage potential candidates, ensuring a seamless recruitment process
Collaborate for Success: Partner with hiring managers to understand their specific talent needs, providing expert guidance throughout the recruitment journey
Elevate Candidate Experience: Ensure candidates have a positive experience, from initial contact to seamless onboarding
As a Recruiter , you will: Identify Top Talent: Utilize diverse channels to source and engage potential candidates, ensuring a seamless recruitment process
Collaborate for Success: Partner with hiring managers to understand their specific talent needs, providing expert guidance throughout the recruitment journey
Elevate Candidate Experience: Ensure candidates have a positive experience, from initial contact to seamless onboarding
You will be supervising the Quality Technicians and Quality Engineers
You will be responsible for driving and implementing process improvements to ensure predictable processes across all product lines (e.g. Risk Reduction, Yield improvements, Customer complaint reduction, Error proofing, Cost Reduction initiatives, Process Automation activities)
You will provide effective and responsive QA support to Operations to meet their area’s objectives of quality, cost and output
Ensure all process variables and their interactions are adequately defined. Ensure all failure modes in process have been identified and addressed. (e.g. Use of DOE studies, FMEA’s)
You wil be responsible for ensuring Regulatory compliance in area of responsibility to cGMP’s of all medical device regulatory agencies (e.g. FDA and TUV)
You will define process and product validation requirements, preparation and approval of Master Validation Plans, protocols and reports approval
You will be reviewing MRB trends and identification of appropriate corrective actions when required
You'll be required to perform internal quality audits
Provide effective and responsive QA support to Operations to meet their area’s objectives of quality, cost and output
Ensure all process variables and their interactions are adequately defined. Ensure all failure modes in process have been identified and addressed. (e.g. Use of DOE studies, FMEA’s)
Ensure Regulatory compliance in area of responsibility to cGMP’s of all medical device regulatory agencies (e.g. FDA and TUV)
Identification and implementation of appropriate statistical techniques to monitor process performance (e.g. SPC, CpK analysis, sampling techniques)
Approval of change requests for product, process and quality system changes
Validation: Define process, product and test method validation requirements, preparation and approval of Master Validation Plans, protocols and reports approval
Compilation of required Regulatory documentation
Perform internal quality audits
Transfer and implement product and processes from development or from another manufacturing facility
This newly created job is an excellent opportunity to join the high performing Life Sciences team in Lublin (Poland) & Cork (Ireland)
Influencing and guiding candidates and clients on the trends across the Life Sciences sector
Candidate management and tracking, including all administration, payroll tasks, compliance and reference checks
Maintaining a full and active pipeline of talent for speculative selling and job filling – candidate sourcing, screening, interview preparation and coaching through the process
You will be responsible for negotiation of rates and business terms with new clients
Pitching the Sigmar Recruitment service offering and presenting this to current and prospective clients
Playing a vital role in increasing the team’s revenue potential by winning new jobs and delivering on the service offering
New and regeneration business development activities including market mapping, prospecting clients, and maintaining consistent communication
Provide effective and responsive QA support to Operations to meet their area’s objectives of quality, cost and output
Ensure all process variables and their interactions are adequately defined. Ensure all failure modes in process have been identified and addressed. (e.g. Use of DOE studies, FMEA’s)
Ensure Regulatory compliance in area of responsibility to cGMP’s of all medical device regulatory agencies (e.g. FDA and TUV)
Identification and implementation of appropriate statistical techniques to monitor process performance (e.g. SPC, CpK analysis, sampling techniques)
Approval of change requests for product, process and quality system changes
Validation: Define process, product and test method validation requirements, preparation and approval of Master Validation Plans, protocols and reports approval
Compilation of required Regulatory documentation
Perform internal quality audits
Transfer and implement product and processes from development or from another manufacturing facility