Introduction
Werfen is a growing family-owned innovative company founded in 1966 in Barcelona Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis Acute Care Diagnostics Transfusion Autoimmunity and Transplant. Through our Original Equipment Manufacturing (OEM) business line we research develop and manufacture customized assays and biomaterials. We operate directly in 30 countries and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe and our workforce is more than 7000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas our commitment to customers and our dedication to innovation and quality. Were passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care
Overview
We are looking to hire a Biologics Procurement Manager who will manage all tasks and functions associated with Biologics Procurement and Manufacturing Training. This includes managing the supply of red blood cells and other blood products needed for Werfens Red Cell and Capture product line. This person will also manage activities associated with training new employees and cross-training or re-training current employees as needed for Red Cell Processing Monoclonal Production Production Support Controlled Components Solid Phase Vialing and Packaging. If youve got the necessary skills and experience to excel in this position we want to hear from you. Apply today!
This position is not eligible for sponsorship for work authorization by Immucor Inc. Therefore if you will require sponsorship from us for work authorization now or in the future we cannot consider your application at this time.
Manager Biologics Procurement and Manufacturing Training
Responsibilities
As the Manager Biologics Procurement and Manufacturing Training you will be responsible for managing the process for securing the supply of red blood cells and other blood products needed for Immucors Red Cell and Capture product line and ensuring all products meet stringent specifications. You will ensure all new hire training and cross-training or re-training for current employees are compliant within GMP/Quality. Regulatory training areas. You will assist in the design development and execution of manufacturing process training for manufacturing personnel. You will support corporate expectations while maintaining compliance with GMP Quality and Regulatory guidelines for the medical device industry.
Your essential duties and responsibilities include:
- Ensures the continued maintenance of inventory levels for red blood cells and other blood products needed to meet production needs.
- Provides direct supervision scheduling of department staff and manages all daily activities of the departments.
- Ensure that the activities of each department are organized timely and completed according to department procedures or protocols. Ensure all departmental scheduling meets company requirements.
- Completes timely review of department and staff records and ensures department records are legible complete and stored according to company procedures.
- Performs and documents department employee training and competency assessment in a timely manner.
- Make daily decisions with regard to the operations of the Biologics Procurement and Manufacturing Training department.
- Conduct interviews for new hires and provide feedback and evaluations for current staff including disciplinary actions when required.
- Maintains departmental procedure manuals and completes required reviews of SOPs and other controlled documents as required by company policy.
- Maintain thorough understanding of and ensures staff adherence to all required safety standards/regulations and bio-hazardousdisposal procedures in accordance with Safety and Environment regulations.
- Understands GMP and ISO 13485 requirements for the manufacture of in vitro Diagnostic Devices and standards relating to large scale cell culture processes for the manufacture of IVDDs.
- Ensures staff compliance with applicable company policies procedures and regulatory requirements.
- Maintains an active commitment to continuing education (attending national state or local meetings or completing courses) not including attending in-house education functions and independent study sessions.
- Understands the source composition and characteristics of raw materials components final products and associated chemical and biosafety hazards for Red Cell and Capture Products.
- Understands Biologics Procurement lab processes and equipment including required maintenance cleaning and operational procedures necessary to maintain GMP compliance.
- Ensures staff compliance with all company required safety practices.
- Responsible for the planning development and incorporation of new and improved processes applicable to the department including deviation management.
- Maintains a general understanding of the activities of all company departments.
- Ensures the continued maintenance of neat organized clean departments. Maintains organized documentation and files.
- Interacts cooperatively and positively with co-workers and the employees of other departments and receives direction well from superiors.
Employee Competency Assessment:
- Manage activities associated with assessing competency of incumbent employees in manufacturing on an annual basis.
- Responsible for documenting all competency assessments and submitting training records to L&D in a timely manner.
- Responsible for maintaining his/her own competency for all required processes and procedures.
Manager Biologics Procurement and Manufacturing Training
Qualifications
We are looking for a Manager Biologics Procurement and Manufacturing Training who will manage 4-6 employees organize schedule and supervise the daily operationsof the Biologics Procurement department including Survey Production. Manager or assists in all areas of the Biologics Procurement lab ensure appropriate completion of departmental equipment quality control validation studies process improvement and ongoing assessment for department trainers assessing competence and submitting training records to L & D in a timely manner.
Specific qualifications for the role include:
- Bachelors degree (BS/BA) with emphasis in Biology Microbiology or Chemistry from four-year college or university; or equivalent combination of education and experience.
- Minimum 1-3 years experience in a GMP environment required.
- MT/CLS/Blood Bank Reference Lab/SBB preferred.
- 2-3 years Transfusion Service or science degree with industry experience preferred
- Previous supervisory experience in manufacturing or Quality Control experience preferred
- Must be available to work irregular hours including weekends and overtime as necessary to meet company requirements and production demands. May be required to cover additional responsibilities and/or provide consultation and/or assistance in off-hours.
- Experience with extended red cell antigens and their characteristics preferred
- Strong attention to detail and ability to summarize and communicate at all levels of the organization.
- Experience with Excel SharePoint Outlook preferred
- Facilitation experience
Manager Biologics Procurement and Manufacturing Training
Closing
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination harassment or retaliation based upon an individuals race color religion gender sexual orientation gender identity/expression national origin/ancestry age mental/physical disability medical condition marital status veteran status or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process please contact for assistance.
We operate directly in over 30 countries and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7000 employees around the world comprise our Werfen team.
Required Experience:
Manager
IntroductionWerfen is a growing family-owned innovative company founded in 1966 in Barcelona Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis Acute Care Diagnostics Transfusion Autoimmunity and Transplant. Through our Original Equipment Manufacturing (OEM) busin...
Introduction
Werfen is a growing family-owned innovative company founded in 1966 in Barcelona Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis Acute Care Diagnostics Transfusion Autoimmunity and Transplant. Through our Original Equipment Manufacturing (OEM) business line we research develop and manufacture customized assays and biomaterials. We operate directly in 30 countries and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe and our workforce is more than 7000 strong.
Our success comes from a specific focus in these rapidly evolving diagnostic areas our commitment to customers and our dedication to innovation and quality. Were passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care
Overview
We are looking to hire a Biologics Procurement Manager who will manage all tasks and functions associated with Biologics Procurement and Manufacturing Training. This includes managing the supply of red blood cells and other blood products needed for Werfens Red Cell and Capture product line. This person will also manage activities associated with training new employees and cross-training or re-training current employees as needed for Red Cell Processing Monoclonal Production Production Support Controlled Components Solid Phase Vialing and Packaging. If youve got the necessary skills and experience to excel in this position we want to hear from you. Apply today!
This position is not eligible for sponsorship for work authorization by Immucor Inc. Therefore if you will require sponsorship from us for work authorization now or in the future we cannot consider your application at this time.
Manager Biologics Procurement and Manufacturing Training
Responsibilities
As the Manager Biologics Procurement and Manufacturing Training you will be responsible for managing the process for securing the supply of red blood cells and other blood products needed for Immucors Red Cell and Capture product line and ensuring all products meet stringent specifications. You will ensure all new hire training and cross-training or re-training for current employees are compliant within GMP/Quality. Regulatory training areas. You will assist in the design development and execution of manufacturing process training for manufacturing personnel. You will support corporate expectations while maintaining compliance with GMP Quality and Regulatory guidelines for the medical device industry.
Your essential duties and responsibilities include:
- Ensures the continued maintenance of inventory levels for red blood cells and other blood products needed to meet production needs.
- Provides direct supervision scheduling of department staff and manages all daily activities of the departments.
- Ensure that the activities of each department are organized timely and completed according to department procedures or protocols. Ensure all departmental scheduling meets company requirements.
- Completes timely review of department and staff records and ensures department records are legible complete and stored according to company procedures.
- Performs and documents department employee training and competency assessment in a timely manner.
- Make daily decisions with regard to the operations of the Biologics Procurement and Manufacturing Training department.
- Conduct interviews for new hires and provide feedback and evaluations for current staff including disciplinary actions when required.
- Maintains departmental procedure manuals and completes required reviews of SOPs and other controlled documents as required by company policy.
- Maintain thorough understanding of and ensures staff adherence to all required safety standards/regulations and bio-hazardousdisposal procedures in accordance with Safety and Environment regulations.
- Understands GMP and ISO 13485 requirements for the manufacture of in vitro Diagnostic Devices and standards relating to large scale cell culture processes for the manufacture of IVDDs.
- Ensures staff compliance with applicable company policies procedures and regulatory requirements.
- Maintains an active commitment to continuing education (attending national state or local meetings or completing courses) not including attending in-house education functions and independent study sessions.
- Understands the source composition and characteristics of raw materials components final products and associated chemical and biosafety hazards for Red Cell and Capture Products.
- Understands Biologics Procurement lab processes and equipment including required maintenance cleaning and operational procedures necessary to maintain GMP compliance.
- Ensures staff compliance with all company required safety practices.
- Responsible for the planning development and incorporation of new and improved processes applicable to the department including deviation management.
- Maintains a general understanding of the activities of all company departments.
- Ensures the continued maintenance of neat organized clean departments. Maintains organized documentation and files.
- Interacts cooperatively and positively with co-workers and the employees of other departments and receives direction well from superiors.
Employee Competency Assessment:
- Manage activities associated with assessing competency of incumbent employees in manufacturing on an annual basis.
- Responsible for documenting all competency assessments and submitting training records to L&D in a timely manner.
- Responsible for maintaining his/her own competency for all required processes and procedures.
Manager Biologics Procurement and Manufacturing Training
Qualifications
We are looking for a Manager Biologics Procurement and Manufacturing Training who will manage 4-6 employees organize schedule and supervise the daily operationsof the Biologics Procurement department including Survey Production. Manager or assists in all areas of the Biologics Procurement lab ensure appropriate completion of departmental equipment quality control validation studies process improvement and ongoing assessment for department trainers assessing competence and submitting training records to L & D in a timely manner.
Specific qualifications for the role include:
- Bachelors degree (BS/BA) with emphasis in Biology Microbiology or Chemistry from four-year college or university; or equivalent combination of education and experience.
- Minimum 1-3 years experience in a GMP environment required.
- MT/CLS/Blood Bank Reference Lab/SBB preferred.
- 2-3 years Transfusion Service or science degree with industry experience preferred
- Previous supervisory experience in manufacturing or Quality Control experience preferred
- Must be available to work irregular hours including weekends and overtime as necessary to meet company requirements and production demands. May be required to cover additional responsibilities and/or provide consultation and/or assistance in off-hours.
- Experience with extended red cell antigens and their characteristics preferred
- Strong attention to detail and ability to summarize and communicate at all levels of the organization.
- Experience with Excel SharePoint Outlook preferred
- Facilitation experience
Manager Biologics Procurement and Manufacturing Training
Closing
If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV.
Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination harassment or retaliation based upon an individuals race color religion gender sexual orientation gender identity/expression national origin/ancestry age mental/physical disability medical condition marital status veteran status or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process please contact for assistance.
We operate directly in over 30 countries and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7000 employees around the world comprise our Werfen team.
Required Experience:
Manager
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