Manufacturing Specialist

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USWM, LLC

Posted 3 months ago

Full Time

Philadelphia, Pennsylvania

In Person

Smart Summary

Responsibilities

The Manufacturing Specialist performs aseptic cell processing, media formulation, and product sampling within a cGMP cleanroom environment. They are also responsible for documenting production operations, maintaining batch records, and training junior staff on unit operations.

Qualifications

We are looking for a Manufacturing Specialist with a Bachelor's degree in cell biology, bioengineering, medical technology, or equivalent experience. The role involves performing cell processing activities, media formulation, and product sampling in an aseptic cGMP environment. Candidates should have at least 1 year of experience working with Advanced Cell Therapies within a cGMP environment and possess strong GMP/GDP understanding and excellent communication skills.

Job Description

This role exists to provide support for the 1st shift manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory.

DUTIES AND RESPONSIBILITIES:  

The following reflects management’s definition of essential functions for this job but does not restrict the tasks that may be assigned.  Management may assign or reassign duties and responsibilities to this job at any time due to reasonable accommodation or other reasons.

  • Performs cell manufacturing related activities while wearing clean room attire in an aseptic cGMP manner. SME on unit operations. Documents production operations in corresponding batch records and logbooks per established procedures ensuring accuracy and timely completion. Identifies real-time manufacturing issues (deviations and atypical results) and communicates them to Manufacturing Management and the Quality team in a timely manner.
  • Authors or edit SOPs, batch records, training records, logbooks, validation plans and technical reports as assigned. Handles human blood and human blood-based product intermediates; Helps with warehouse management, critical reagents and material inventory reports.
  • Work on project teams (continuous improvement initiatives)
  • Inputting and uploading of manufacturing data in real time to existing database.
  • Review of Batch Records and logbooks / comment resolution.
  • Train new or junior employees on equipment and unit operations.

QUALIFICATIONS: 

  • Bachelor’s degree in a cell biology, bioengineering or medical technology related field, or equivalent experience is required. 
  • Minimum 1 year working with Advanced Cell Therapies withing a cGMP environment 
  • Ability to work flexible hours with some night and weekend availability is required. This is a start-up situation so schedules and shifts will change over time. 
  • Demonstrated strong understanding of GMP/GDP (21 CFR Part 210/211 & 21CFR Part 11) 
  • Ability to stand for multiple hours and lift 20 pounds. 
  • Experience working in an aseptic cleanroom with full aseptic gowning. 
  • Excellent verbal and written communication skills are required. 
  • Computer literacy is required including Microsoft Outlook, Word, Excel and Power Point. 

COMPETENCIES:  

  • Adaptability - Adapts to changes in the work environment; Manages competing demands; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events.
  • Attendance/Punctuality - Is consistently at work and on time; Ensures work responsibilities are covered when absent; Arrives at meetings and appointments on time. 
  • Computer Skills – Skilled with computers; Takes advantage of new technology; Learns new tools quickly; Uses technology to enhance job performance.
  • Conflict Management – Good listener; Committed to finding solution to problems; Works well with people.
  • Dependability - Follows instructions, responds to management direction; Takes responsibility for own actions; Keeps commitments; Commits to long hours of work when necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan. 
  • Judgment - Displays willingness to make decisions; Exhibits sound and accurate judgment; Supports and explains reasoning for decisions; Includes appropriate people in decision-making process; Makes timely decisions.
  • Motivation - Sets and achieves challenging goals; Demonstrates persistence and overcomes obstacles; Measures self against standard of excellence; Takes calculated risks to accomplish goals.
  • Oral Communication - Speaks clearly and persuasively in positive or negative situations; Listens and gets clarification; Responds well to questions; Demonstrates group presentation skills; Participates in meetings. 

The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

PHYSICAL DEMANDS:

  • Frequently required to stand
  • Frequently required to walk. 
  • Frequently required to sit. 
  • Frequently required to talk or hear. 
  • Occasionally required to lift light weights (less than 25 pounds) 
  • Specific vision abilities required for this job include: close vision, color vision and ability to adjust or focus

WORK ENVIRONMENT: 

  • The noise level in the work environment usually is quiet.

Equal opportunity employer, and does not discriminate on the basis of race, color, religion, sex, pregnancy, national origin, disability, age, genetic information, veteran status, sexual orientation, gender identity or any other characteristic protected by federal, state or local law.

U

USWM, LLC

US WorldMeds is a specialty pharmaceutical company that develops, licenses, and brings to market unique healthcare products designed to improve the lives of patients with challenging conditions and unmet medical needs. Organized on March 23, 2001 by current CEO Paul Breckinridge "Breck"​ Jones, US WorldMeds holds true to Breck’s vision of creating a sustainable, privately held specialty pharmaceutical company known for agility and personal attention to its products and stakeholders. Our dedication to improving patients’ lives can be seen both in the products that we market and the therapies that are currently under development. Each day, we work diligently to bring new therapies and new indications to patients across multiple therapeutic areas. In addition to our dedication to serving patients, we embrace a culture that values honesty, creativity, and action, integrity in relationships, a passion for success, and good stewardship of Company resources. We offer our employees exciting challenges, unique opportunities, and a fast-paced environment that emphasizes innovation and achievement. Our headquarters are in Louisville, Kentucky, but you can find our team and partners throughout the U.S. and across the globe. To learn more about our mission and values, and for all US WorldMeds information, visit our site: http://www.usworldmeds.com. You can also follow us on Twitter at @USWorldMeds.
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