Qureos Mentor

KBI Biopharma

<div><div>Job Summary:</div><div>
The Sr. Manufacturing Associate I/II is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment. The Sr. Manufacturing Associate I/II must follow the instructions depicted in SR&rsquo;s, EPR&rsquo;s, BR&rsquo;s, SOP&rsquo;s and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including &lsquo;Right the First Time&rsquo; (RFT). Identify possible process and record improvements and communicate this to the appropriate personnel.</div><div>
The ideal candidate will be both technically sound and have a quality mindset. The candidate will use and demonstrate their past experiences and knowledge of cell culture Upstream or Downstream fundamentals in cell culture media preparation, shake flask operations, seed expansion, bioreactor setup and operations, cell culture harvest setup and operations, aseptic technique, chromatography, ultrafiltration, and drug substance filling operations; as well as in analytical tools and general biotechnology auxiliary equipment (pumps, sterile tubing welders and sealers, pH/Conductivity/osmolarity meters) to teach, troubleshoot and continuously improve the daily operations of manufacturing. The Sr. Manufacturing Associate I/II will promote and enforce precise and compliant operations.</div><div>
The Sr. Manufacturing Associate I/II will maintain a sense of ownership of the production processes, manufacturing environment and facility. Following task execution, the Sr. Manufacturing Associate I/II will review the executed production records (SR&rsquo;s, ERP, and BR&rsquo;s) to ensure a comprehensive and accurate set of actions have occurred. It is management&rsquo;s expectation that any deviations/events are documented and escalated to the Management and Quality system according to KBI internal notification processes.</div><div></div><div>
The normal work hours for this position are 7:00 pm - 7:00 am. on a 3 - 3 -2 work schedule.</div><div></div><div>
Job Description</div><div>
Manufacture cell culture products per manufacturing batch records and in compliance with quality standards, company policies and current regulations. Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.</div><div>
Document each task involving manufacturing procedures (i.e. SR&rsquo;s, EPR&rsquo;s and BR&rsquo;s) following GDP at the time of execution. Utilize and perform maintenance on equipment per applicable SOP. Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR). Demonstrate, apply and ensure understanding of current Good Manufacturing Practices and how they apply to specific tasks and responsibilities. Participate and be accountable for room 5S. Provide direction/guidance to Manufacturing Associate I and Manufacturing Associate II, Senior Manufacturing Associate I and Senior Manufacturing Associate II. Help supervisor to distribute the workload and ensure others understand the requirements of their tasks.</div><div></div><div>
Education / Previous Experience:</div><div>
Sr. Manufacturing Associate I</div><ul><li><div>
Bachelor&rsquo;s degree in a related scientific or engineering discipline with 4-6 years&rsquo; experience in related GMP manufacturing operations; or high school diploma with 7-10 years&rsquo; experience in related GMP manufacturing operations.</div></li></ul><div></div><div>
Sr. Manufacturing Associate II</div><ul><li><div>
Bachelor&rsquo;s degree in a related scientific or engineering discipline and 5+ years&rsquo; experience in related GMP manufacturing operations; or high school diploma with 10+ years&rsquo; experience in related GMP manufacturing operations.</div></li></ul><div></div><div>
Knowledge, Skills, Abilities:</div><ul><li><div>
Demonstrated knowledge of cell culture, fermentation or purification unit operation is preferred. Experience in single-use platform technology is preferred.</div></li><li><div>
Excellent written and verbal communication skills are required.</div></li><li><div>
Energetic, motivated and dynamic individual.</div></li><li><div>
Must be organized and able to focus in a face-paced, multi-tasked environment and maintain operational efficiency and positive demeanor.</div></li></ul><div></div><div>
Language Ability</div><ul><li>
Fluent in English language both reading and writing.</li><li>
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, procedure manuals, batch and production records.</li><li>
Ability to write routine reports and correspondence.</li><li>
Ability to speak effectively before groups of customers or employees of organization.</li></ul><div></div><div>
Reasoning Ability</div><ul><li>
Ability to solve practical problems and deal with a variety of concrete variables in</li><li>
situations where only limited standardization exists. Ability to interpret a variety of</li><li>
instructions furnished in written, oral, diagram, or schedule form.</li></ul><div></div><div>
Math Ability</div><ul><li>
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.</li><li>
Ability to compute rate, ratio, and percent and to draw and interpret graphs.</li></ul><div></div><div>
Physical Demands</div><ul><li>
Standing and sitting for long periods of time may be required at times.</li><li>
Lifting, pushing, and pulling may be required for stocking and movement of equipment.</li><li>
The use of ladder may be required when setting up bioreactors.</li></ul><div></div><div>
Computer Skills</div><ul><li>
Knowledge or and experience using MS Office, ERP, EDMS, production equipment software</li></ul><div></div><div>
Equipment Use</div><ul><li>
Experience or knowledge using equipment - (Examples include Biosafety Cabinets, Incubators, Single Use Bioreactors, Chromatography Columns/Skids, Ultrafiltration Skids, Filling systems, Peristaltic Pumps and Other Single Use pumps, Automated Cell Counters, Blood Gas Analyzers, Metabolite Analyzers, Scales and Balances, pH and Osmolality meters, other lab, production, and office equipment.)</li></ul><div></div><div>
Working Schedule: - 7PM -7AM / 2-2-3 schedule</div><ul><li>
The normal working hours for this position are 7:00 pm - 7:00 am.</li><li>
The job requires working 12-hour shifts which may include working overnight.</li><li>
The job's schedule is a rotating 3-3-2 work schedule.</li></ul><div></div><div>
Working Conditions:</div><ul><li>
The job requires working within a cGMP manufacturing biotechnology facility which requires clean room operations. Clean room operations require donning clean room attire when entering clean room areas and maintaining good personal hygiene.</li><li>
While performing the duties of this job the employee regularly utilizes equipment and materials which include mechanical hazards, chemical hazards, , electricity hazards, and tripping and falling hazards.</li><li>
The noise level in the environment is moderate to high.</li></ul><div></div><div>
KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching, and employee recognition programs.</div><div>
About KBI:</div><div>
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit <div>www.kbibiopharma.com</div>.</div><div></div><div><i>
KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds &ndash; regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status &ndash; and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.</i></div><div></div><div><i>
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.</i></div><div></div><div><i>
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.</i></div><div></div><div><i>
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.</i></div></div>

Senior Manufacturing Associate 1 / II

<div><div>Job Summary:</div><div>
The MQA Manager/Sr. Manager is responsible for supervising the MQA team who supports the Manufacturing Process and Areas as part of a GMP Contract Manufacturing Organization. MQA Manager/Sr. Managers are expected to provide sound guidance to internal MQA team and customers with respect to process, SISPQ of product, and risk. The MQA Manager/Sr. Manager&rsquo;s team shares responsibility for the inspection readiness of the site. MQA Manager/Sr. Manager routinely work on the cleanroom floor directly with the MQA and Manufacturing team to provide real time guidance and support. The Manager/Sr. Manager must adhere to procedures and policies to work on the Manufacturing floor. MQA Manager/Sr. Manager routinely collaborates with Manufacturing and work on team initiatives. The MQA Manager/Sr. Manager is responsible for coaching and mentoring their teams as needed to foster a GMP compliant site.</div><div></div><div>
Job Responsibilities:</div><ul><li>
Lead, assess, mentor, and develop departmental associates. Level load work across team to ensure timely review/approval of Quality items in support of manufacturing and batch release timelines. Manage performance; ensure team meets expectations and meets objectives; guide the professional growth of team members by providing personal guidance and training relative to responsibilities. Coach QA Specialists to achieve proficiency for the process execution, reviewing/approving executed process records SOPs, DTRs and Deviations.</li><li>
Manage the process proficiency for the site. Oversee MQA support of Manufacturing. Work directly with functional areas to review and approve process procedures. Report KPI&rsquo;s and collaborate with functional areas to improve the Site Quality Systems and streamline processes.</li><li>
Coordinate client communications for batch record comment resolution. Address client comments with internal SMEs and driving client approvals. Represent Quality in required client meetings, which includes obtaining client metrics and presenting in client meetings.</li><li>
Attend relevant operational meetings in support of Manufacturing Operations and disposition activities.</li><li>
Support Client Audits and Regulatory Inspections as required.</li></ul><div></div><div><br>
Minimum Requirements:</div><div>
Knowledge, Skills, Abilities</div><ul><li>
BS and 10+ years&rsquo; experience (Manager), MS and 8+ years&rsquo; experience (Sr Manager) in a QA or cGMP environment in Biopharmaceuticals or equivalent.</li><li>
Experience in providing Quality guidance to manufacturing to include Deviations/CAPAs and Change Controls, with 4+ years of supervisory experience.</li><li>
Demonstrates strong interpersonal skills, ability to work in a team environment, attention to details, and excellent problem resolution skills.</li><li>
Strong understanding of FDA, EU, and ROW cGMP regulations.</li><li>
Experience and knowledge of worldwide regulatory requirements with emphasis on regulatory requirements for biotechnology-derived product.</li></ul><ul><li>
Experience managing data, metrics, and presenting to senior management.</li><li>
Demonstrate strong interpersonal skills, ability to work in a team environment, attention to details, and excellent problem resolution skills.</li><li>
Demonstrated track record in the following key areas:</li></ul><ul><li>Strong orientation for Quality and Customer Service</li><li>Demonstrated level of respect for individuals</li><li>High level of integrity and personal responsibility</li><li>Record of innovation</li><li>Strong collaboration and team building skills.</li></ul><div></div><div>
Language Ability</div><ul><li>
Ability to read, analyze, and interpret English documents.</li><li>
Ability to respond effectively to the most sensitive inquiries or complaints.</li><li>
Ability to write technical correspondence that is easy to follow and understand.</li><li>
Ability to make effective and persuasive presentations on controversial or complex topics to senior management peer group, employee groups, and customers.</li></ul><div>
Reasoning Ability</div><ul><li>
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.</li><li>
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.</li></ul><div>
Math Ability</div><ul><li>
Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems.</li><li>
Ability to deal with a variety of abstract and concrete variables in situations where only limited standardization exists.</li></ul><div>
Physical Demands</div><ul><li>
Use of hands and fingers to manipulate office equipment is required. Position may require sitting or standing for long hours of time.</li><li>
Support manufacturing and warehouse operations to include movement, gowning, and/or lifting</li></ul><div>
Computer Skills</div><ul><li>
Proficient in Microsoft Excel, Microsoft Word, Outlook, PowerPoint, and Internet.</li><li>
Ability to use enterprise software, such as Document Management Systems, Learning Management Systems, Asset Management Systems, Electronic Lab Notebooks, Enterprise Resource Planning systems or similar programs.</li></ul><div>
Equipment Use</div><ul><li>
Knowledge of and experience using a Computer, Telephone, Copier, Printer, Scanner</li></ul><div></div><div><i>
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.</i></div><div></div><div><i>
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.</i></div><div></div><div><i>
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.</i></div></div>

KBI: US - Manager, QA

<div><div>Job Summary:</div><div>
Responsible for providing Quality Assurance support to Manufacturing Process Operations. Performs document review and approval of Master Batch Records, SOP&rsquo;s and Technical Documents. Collaborate directly with MS&amp;T and Manufacturing to support BOM review and approvals to meet timelines.</div><div></div><div>
Job Responsibilities:</div><ul><li>
Supports BOM review, approval, and release within ERP system</li><li>
Reviews and approves Technical Documents associated with process validation and manufacturing operations, including but not limited to the following document types: Process Characterization, Process Performance Qualification, Resin and Membrane Qualifications, and Non-routine Sample Plans.</li><li>
Provides general QA support to manufacturing operations, which includes deviation investigations, CAPAs, procedures and change control assessments, as required.</li><li>
Performs compliance review of executed batch records and internal support records, as needed.</li><li>
Attend relevant project and operational meetings. Support client audits, client meetings, regulatory inspections, and process improvement projects, as required.</li><li>
Supports training and mentoring of other Quality department staff to perform quality duties, as needed.</li></ul><div></div><div>
Minimum Requirements:</div><div>
Knowledge, Skills, Abilities</div><ul><li>
BS and 10+ years&rsquo; experience or equivalent or MS and 8+ years&rsquo; experience in a QA cGMP regulated environment within Biopharmaceuticals or equivalent.</li><li>
Experience in a QA role supporting Manufacturing Process Operations and validations is required.</li><li>
Knowledge of US, EU and cGMP guidelines is required.</li><li>
Working knowledge of electronical management systems,</li><li>
Operational Excellence tools and ERP systems is desired.</li></ul><div></div><div>
Language Ability</div><ul><li>
Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.</li><li>
Ability to write reports, business correspondence, and procedure manuals.</li><li>
Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.</li></ul><div></div><div>
Reasoning Ability</div><ul><li>
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.</li><li>
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.</li></ul><div></div><div>
Math Ability</div><ul><li>
Basic math skills are required.</li><li>
Ability to apply concepts of basic algebra and statistics.</li></ul><div></div><div>
Physical Demands</div><ul><li>
Be able to sit for long periods of time.</li><li>
Be able to lift 20 pounds.</li></ul><div></div><div>
Computer Skills</div><ul><li>
Knowledge of and experience using word processing, databases, spreadsheets, PowerPoint, Excel, internet, e-mail, calendar management, Teams and Sharepoint.</li></ul><div></div><div>
Equipment Use</div><ul><li>
Knowledge of and experience using a computer, and a telephone</li></ul><div></div><div><i>
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.</i></div><div></div><div><i>
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.</i></div><div></div><div><i>
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.</i></div></div>

KBI: US - Principal QA Specialist - Product Support

<div><div>At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact.</div><div></div><div><br>
Position Summary:</div><div>
Effectively leads a team within Program Management or large Project Management function, ensures appropriate development and control of related processes and systems. With personal responsibility for a portfolio, the role holder is the primary client account and relationship manager for KBI PMO, driving business delivery and exemplary client service to maximum benefit for the company in a sustainable manner. The incumbent may provide training and mentorship to others.</div><div></div><div><br>
Responsibilities:</div><div>
Client Management</div><ul><li><div>
Oversees increased complexity in demand of projects, such as government- supported programs (BARDA, DOD etc), high profile clients of strategic importance.</div></li></ul><ul><li><div>
Responsible for relationship and account management for assigned clients/portfolios plus oversight of projects managed by direct reports.</div></li></ul><ul><li><div>
Provides sound judgments and technical / regulatory recommendations on drug development to clients.</div></li></ul><ul><li><div>
Cultivates Client relationship. Provides timely and appropriate reporting of Issues/Risks to leadership.</div></li></ul><ul><li><div>
Manages client expectations efficiently. Maintains strong working relationships with all client representatives. Able to mend and/or develop client relationships.</div></li></ul><ul><li><div>
Supports PM-VOC process; recommends and/or implements initiatives to identify and address opportunities to improve client service.</div></li></ul><ul><li><div>
Primary point of contact for all Client communications and coordination of third- party vendor and project needs.</div></li></ul><div>
Program Management</div><ul><li><div>
Manages project timelines through all phases of development, from project award and kick-off through close-out.</div></li></ul><ul><li><div>
Ensures that projects are conducted on time, within scope and budget, and meet Client agreed- upon quality standards and expectations through cross- functional project team alignment.</div></li></ul><ul><li><div>
Develops, manages, and updates project plans in a timely manner. Communicates project status, progress, timelines, changes in schedule, scope changes, technical and/or quality issues to all relevant personnel in the company, and with the Client.</div></li></ul><ul><li><div>
Schedules, facilitates and documents program related client team meetings, including issuance of agenda, action items, meeting minutes, client communications, etc.</div></li></ul><ul><li><div>
Leads cross-functional teams without direct authority by casting a clear vision of project objectives/priorities and motivate the team to achieve them. Able to resolve conflict and foster collaborative partnerships with others to achieve peak performance with minimal assistance from manager or delegate.</div></li></ul><ul><li><div>
Analyzes risk, establishes contingency plans and identifies trigger events and responsibility for initiating mitigating action. Gathers stakeholder input and ranks the top project risks in terms of total impact.</div></li></ul><ul><li><div>
Facilitates discussion regarding portfolio priorities (resolving resource conflicts).</div></li></ul><ul><li><div>
Participates in strategic initiatives for PMO and Clients. Able to suggest and champion the implementation of improvements to systems and processes.</div></li></ul><ul><li><div>
Promotes KBI capabilities and manages business discussions.</div></li></ul><div>
Staff Management</div><ul><li><div>
May have up to 4 direct reports which may include leadership levels that also have direct reports.</div></li></ul><ul><li><div>
Monitor and manage staff compliance to PMO project delivery processes.</div></li></ul><ul><li><div>
Support appropriate development of staff providing training and mentoring in line with their role and experience.</div></li></ul><ul><li><div>
Accurately evaluate the performance levels of direct reports and communicate openly with constructive feedback to develop potential.</div></li></ul><ul><li><div>
May participate in panel interviews of Program Manager candidates.</div></li></ul><div>
Business/Financial Management</div><ul><li><div>
Schedules and facilitates strategic client discussions and Joint Steering Committee meetings as required with Senior/Executive Leadership participation and support. Generates meeting minutes and actions items for follow-up.</div></li></ul><ul><li><div>
Manages the technical and strategic development of the program drawing on relevant Technical leadership from across the organization. This process includes generating and presenting resulting proposals and change orders to the client as appropriate.</div></li></ul><ul><li><div>
Directs and supports the client with project strategy. Able to suggest and be involved in the implementation of improvements to systems and processes; support PMO with PLF readiness as required.</div></li></ul><ul><li><div>
Manages all contractual and financial aspects of the project, including finalization of change order and subsequent amendments, monthly budget reviews, forecasting, materials review, assessment of work performed and appropriate Client invoicing and vendor payments.</div></li></ul><ul><li><div>
Oversees timely revenue management and forecasting; identifies opportunities for gap closure within team and executes accordingly.</div></li></ul><ul><li><div>
Assists Business Development Department in development of proposals as needed.</div></li></ul><div>
PMO Support</div><ul><li><div>
Acts as a contributing member of Program Management Organization.</div></li></ul><ul><li><div>
Leads or contributes to departmental initiatives as appropriate, including procedure development and improvement.</div></li></ul><ul><li><div>
Cross-site portfolio leadership OR process ownership; work with PMO and local team to continuously improve PM and project delivery practices. May own a PMO process, responsible for training tools and associated change management.</div></li></ul><ul><li><div>
Own and manage the site goals and objectives (Balanced Score Card) for self and team.</div></li></ul><ul><li><div>
Represent or deputize for PMO senior staff as required.</div></li></ul><ul><li><div>
Other duties as required.</div></li></ul><div></div><div><br>
Requirements:</div><ul><li><div>
Minimum bachelor&rsquo;s degree required, preferably in science or related discipline MBA or advanced degree a plus.</div></li></ul><ul><li><div>
PMP certification (current or planned in the immediate future).</div></li></ul><ul><li><div>
Minimum 10 years industry experience, with 5 years or more direct project management experience Prior experience effectively managing projects in pharmaceutical or biotech company, CDMO, CRO or related experience required.</div></li></ul><ul><li><div>
Previous personnel management is a plus.</div></li></ul><ul><li><div>
Demonstrated experience in building project management tools/templates, improving project systems and implementing best practices.</div></li></ul><ul><li><div>
Adaptability and flexibility including the ability to manage deadline pressure, ambiguity and change Ability to build teams and generate a spirit of collaboration while coordinating diverse activities and groups.</div></li></ul><ul><li><div>
Familiarity with Good Manufacturing Practices.</div></li></ul><div></div><div><br>
Salary Range: $160,000 - $190,000</div><div>
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate&rsquo;s qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.</div><div>
About KBI:</div><div>
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit <div>www.kbibiopharma.com</div>.</div><div></div><div><i><br>
KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds &ndash; regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status &ndash; and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.</i></div><div></div><div><i>
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.</i></div><div></div><div><i>
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.</i></div><div></div><div><i>
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.</i></div></div>

Associate Director, Program Management

Join KBI Biopharma and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

KBI Biopharma

ABOUT_COMPANY

Senior Manufacturing Associate 1 / II

KBI: US - Manager, QA

KBI: US - Principal QA Specialist - Product Support

Associate Director, Program Management