Production Technician
Production Technician
Posted on :
29-09-2025
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1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
29-09-2025
Job Description
Description:
Internal Client Title: Associate Specialist (Cell Therapy Manufacturing)
Location: Rockville MD
Address: Rockville MD 20850
Duration- 12 months (possibility to extend)
Working Hours/Schedule: 9-5pm
Interview Length: 30 min
Interview Location: Onsite
**In this role contractors must follow proper PPE guidelines outlined by Client.**
Jewelry (including apple watches and fitness bands) are not allowed.
Cosmetics are not allowed except non-pigmented/non-scented basic moisturizer and lip balm.
Nail polish artificial nails eyelash extensions etc are not allowed.
Contactors cannot have recent tattoos or piercings or open wounds.
Introduction:
Associate Specialist (Cell Therapy Manufacturing)
Do you have a passion for science Would you like to apply your expertise to impact a company that follows the science and turns ideas into life changing medicines Then Client might be the place for you!
At Client we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial thinking big and working together to make the impossible a reality. If you are swift to action confident to lead willing to collaborate and curious about what science can do then you re our kind of person.
Summary of the group:
Join the Clinical Manufacturing Cell Therapy Unit and be a part of producing Clients next- generation products as we launch our first wave of cell therapy clinical trials. This position will support the start-up and cGMP operation of the new cell therapy manufacturing facility. Collaboration is key and you will work together frequently with Process Development Clinical Operations Materials Management and Quality Teams.
Main Duties & Responsibilities:
Author and execute manufacturing batch records work instructions and/or SOPs with a focus right the first time . Author and maintain bill of materials. Assist with batch record
reconciliation and timely documentation. Documentation of all activities to meet cGMP
requirements. Assist with deviations/non-conformances/OOS investigations.
Routinely monitor clean prepare and operate sophisticated automated cell processing cell expansion and filling equipment in Grades A & B cleanroom environment.
Train other personnel on aseptic processing equipment operation cGMPs documentation technical theory or other tasks.
Review documentation (batch records SOPs Logbooks) for completeness clarity accuracy and submit edits to documents for revision as needed.
Participate in tech transfer activities. Support process development of platform processes contributing to the plans and designs of studies/experiments. May modify or improve processes and systems depending on purpose of experiments
Provides technical instruction to the team and allocates administrative work where possible assigning tasks to other manufacturing staff leading activities on manufacturing floor communicating to staff about product status at shift change troubleshooting processing and equipment issues.
Ensures a safe work environment in accordance with Client standards.
Weekend work may be required.
Education & Experience Requirements:
Education: Bachelor s or Master s degree in life sciences engineering or a related field
Experience: Bachelor s degree and 0-3 years of general cGMP manufacturing experience Master s degree and 0-2 years of general cGMP manufacturing experience
Required Skills:
Basic knowledge in biologics manufacturing process cell culture and/or vector products.
Technical proficiency in aseptic technique and working with manufacturing equipment in open and closed systems.
Working knowledge of automated manufacturing equipment and/or process analytical
technologies.
Proficiency in Microsoft Word Excel and data analysis.
Desired Skills:
Previous manufacturing or process development experience with cell therapy or vector
products.
Dynamic individual with the ability to communicate and engage others.
Independent and self-starting. Ability to work with minimal supervision.
Demonstrate flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.
Manager Top Must Haves:
Good communication skills (will be working in different rooms and cross functionally so this is really important for success)
Adaptability
Aseptic technique/On the floor manufacturing experience
Why Client
At Client when we see an opportunity for change we seize it and make it happen because any opportunity no matter how small can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we re opening new ways to work pioneering cutting edge methods and bringing unexpected teams together. Interested Come and join our journey.
Enable Skills-Based Hiring No Location: Rockville MD
Address: Rockville MD 20850
Duration- 12 months (possibility to extend)
Working Hours/Schedule: 9-5pm
Interview Length: 30 min
Interview Location: Onsite
**In this role contractors must follow proper PPE guidelines outlined by Client.**
Jewelry (including apple watches and fitness bands) are not allowed.
Cosmetics are not allowed except non-pigmented/non-scented basic moisturizer and lip balm.
Nail polish artificial nails eyelash extensions etc are not allowed.
Contactors cannot have recent tattoos or piercings or open wounds.
Introduction:
Associate Specialist (Cell Therapy Manufacturing)
Do you have a passion for science Would you like to apply your expertise to impact a company that follows the science and turns ideas into life changing medicines Then Client might be the place for you!
At Client we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial thinking big and working together to make the impossible a reality. If you are swift to action confident to lead willing to collaborate and curious about what science can do then you re our kind of person.
Summary of the group:
Join the Clinical Manufacturing Cell Therapy Unit and be a part of producing Clients next- generation products as we launch our first wave of cell therapy clinical trials. This position will support the start-up and cGMP operation of the new cell therapy manufacturing facility. Collaboration is key and you will work together frequently with Process Development Clinical Operations Materials Management and Quality Teams.
Main Duties & Responsibilities:
Author and execute manufacturing batch records work instructions and/or SOPs with a focus right the first time . Author and maintain bill of materials. Assist with batch record
reconciliation and timely documentation. Documentation of all activities to meet cGMP
requirements. Assist with deviations/non-conformances/OOS investigations.
Routinely monitor clean prepare and operate sophisticated automated cell processing cell expansion and filling equipment in Grades A & B cleanroom environment.
Train other personnel on aseptic processing equipment operation cGMPs documentation technical theory or other tasks.
Review documentation (batch records SOPs Logbooks) for completeness clarity accuracy and submit edits to documents for revision as needed.
Participate in tech transfer activities. Support process development of platform processes contributing to the plans and designs of studies/experiments. May modify or improve processes and systems depending on purpose of experiments
Provides technical instruction to the team and allocates administrative work where possible assigning tasks to other manufacturing staff leading activities on manufacturing floor communicating to staff about product status at shift change troubleshooting processing and equipment issues.
Ensures a safe work environment in accordance with Client standards.
Weekend work may be required.
Education & Experience Requirements:
Education: Bachelor s or Master s degree in life sciences engineering or a related field
Experience: Bachelor s degree and 0-3 years of general cGMP manufacturing experience Master s degree and 0-2 years of general cGMP manufacturing experience
Required Skills:
Basic knowledge in biologics manufacturing process cell culture and/or vector products.
Technical proficiency in aseptic technique and working with manufacturing equipment in open and closed systems.
Working knowledge of automated manufacturing equipment and/or process analytical
technologies.
Proficiency in Microsoft Word Excel and data analysis.
Desired Skills:
Previous manufacturing or process development experience with cell therapy or vector
products.
Dynamic individual with the ability to communicate and engage others.
Independent and self-starting. Ability to work with minimal supervision.
Demonstrate flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.
Manager Top Must Haves:
Good communication skills (will be working in different rooms and cross functionally so this is really important for success)
Adaptability
Aseptic technique/On the floor manufacturing experience
Why Client
At Client when we see an opportunity for change we seize it and make it happen because any opportunity no matter how small can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we re opening new ways to work pioneering cutting edge methods and bringing unexpected teams together. Interested Come and join our journey.
Additional Details
- Does the position allow for the worker to be virtual/remote : No
- Critical Position : Yes
- Career Level : B
- External Job Title : (No Value)
Employment Type
Full-time
Key Skills
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