Date Posted: 07/27/2026
Hiring Organization: Rose International
Position Number: 504710
Industry: Medical Equipment & Supplies
Job Title: Manufacturing Technologist - GMP Production
Job Location: Sparks, MD, USA, 21152
Work Model: Onsite
Shift: FRIDAY, SATURDAY AND SUNDAY 6AM TO 6PM
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 13
Min Hourly Rate($): 26.86
Max Hourly Rate($): 26.86
Must Have Skills/Attributes: Manufacturing, Pipetting, Scientist
Experience Desired: Weigh and measure raw materials experience (0-2 yrs); Pipette experience (0-2 yrs); Filtration and dilation experience (0-2 yrs)
Required Minimum Education: High School Diploma or equivalent
Preferred Education: Associate’s Degree
**C2C is not available**
Job Description
Required Equipment:
• Safety Shoes (steel, composite)
Required Education:
• High School degree required
Preferred Education:
• Associates degree with a scientific degree and no experience.
Required Skills and Experience:
• 2 years relevant experience in a regulated environment
• Experience in a regulated environment
• Can effectively work in a team setting and communicate effectively across the department
• Strong attention to detail
• Ability to be punctual in order to ensure production
• Ability to work on assignments that are semi-routine in nature with the skill to recognize any deviations from specification
• Ability to operate independently within the constraints of approved process-related documentation
• Must be proficient in English with the ability to read, write, analyze/evaluate charts, follow simple diagrams and perform basic arithmetic
• Basic proficiency with PCs (Personal Computers) and basic use of a Windows environment
Manufacturing Technologist Responsibilities:
Responsibilities and Duties
• Responsible for manufacturing and assembling clinical and commercial products. Operates production equipment.
• Weighs, measures and checks raw materials to ensure batches manufactured contain proper ingredients and quantities.
• Assists with in-process testing to ensure batches meet specifications.
• Responsible for validating processes and equipment that are directly related to filtration, cleaning and sterilization. Responsible for the removal and disposal of waste chemicals, solvents and acids.
• Creates solutions, powders, and liquids for batches to meet specifications
• Provides training support for on-boarding and/or new procedureso Provides support to the lead/supervisor when necessary
• Provides continuous improvement recommendations and/or solutions to support overall operational efficiency
• Demonstrates the ability to follow established procedures according to Good Manufacturing Practices (GMP)
• Must follow all housekeeping policies and procedures
• Must follow all safety policies and procedures
Must be able to work flexible and/or extended hours and report to work on a regular, punctual basis. Ability to get along with people and be able to work in a team environment. Willingness to rotate into different tasks and responsibilities.
- **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
Rose International maintained good communication during assignments and are very informative through email and phone calls.
Sade, Consultant
It was great working for Rose International. Everyone was extremely helpful.
Rosann, Consultant
I had a very positive experience working for Rose. The entire process is very efficient and easy.
Joanne, Consultant
Your team at Rose International is always very helpful and responsive.
Barbara, Consultant
It is a great pleasure being a part of the Rose International Team.
Toni, Consultant
EMPLOYEE COMMENTS