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Manufacturing Technical Specialist

๐ŸŒŸ Job Opportunity: Manufacturing Technical Specialist ๐ŸŒŸ

๐Ÿ“ Location: Harmans, MD

๐Ÿง‘โ€๐Ÿ”ง Position: 1

๐Ÿ“† Duration: Approximately 2 months

๐Ÿ’ต Pay Rate: $17 to $21/hr (No expenses included)

โœ… Open to locals and USA citizens

๐Ÿข Work Type: 100% ONSITE

๐Ÿ•’ Shift: Mondayโ€“Friday, 8:00 AMโ€“5:00 PM


๐Ÿ’ผ Job Summary

Our client is seeking a Manufacturing Technical Specialist to play a vital role in supporting manufacturing management and associates. This role is critical to ensure batch record reviews, root cause investigations, and GMP document revisions align with patient safety and lot release schedules. Your work will contribute directly to manufacturing life-saving medicinesโ€”prioritizing quality, safety, and on-time delivery.


๐ŸŒŸ Key Responsibilities

โœ”๏ธ Initiate and manage quality records, including deviation investigations, to meet industry standards.

โœ”๏ธ Lead or support investigations using root cause analysis and assess product impact in collaboration with various departments.

โœ”๏ธ Develop, execute, and oversee CAPAs to address process deviations effectively.

โœ”๏ธ Provide technical leadership to ensure investigations meet quality expectations and drive effective corrective actions.

โœ”๏ธ Monitor critical process parameters and provide process monitoring support as needed.

โœ”๏ธ Revise and manage GMP documents such as SOPs and Manufacturing Batch Records.

โœ”๏ธ Drive continuous improvement projects within the manufacturing environment.

โœ”๏ธ Conduct data gathering, trending, and analysis to support investigations.

โœ”๏ธ Offer real-time, on-the-floor support for operational deviations and complete initial event reports.


๐Ÿงช Candidate Qualifications


๐Ÿ“š Education & Experience:

  • Bachelor's degree in a science or engineering field.
  • 4+ years of technical experience in biopharmaceutical manufacturing in a GMP-compliant environment.
  • Hands-on experience with equipment such as incubators, single-use bioreactors, filtration skids, and chromatography skids.\


๐Ÿ›  Skills & Expertise:

  • 3+ years of experience in process deviation investigations and remediation.
  • Strong familiarity with root cause analysis and conducting interviews.
  • Proficiency in authoring and revising technical documents.
  • Ability to support or lead system troubleshooting efforts.


๐ŸŒŸ Key Leadership Attributes:

  • Leads with integrity and respect.
  • Delivers results.
  • Demonstrates business acumen.
  • Fosters collaboration and teamwork.
  • Champions change and innovation.
  • Engages and inspires colleagues.
  • Coaches and develops talent.


โœจ Position Benefits

๐ŸŽฏ Career Growth Potential within a rapidly expanding team.

๐Ÿ“ˆ Defined career path with an annual performance review and feedback process.

๐Ÿ”„ Cross-Functional Exposure to other areas within the organization.

๐Ÿงฌ Gain experience in the cutting-edge gene therapy space.


๐ŸŒŸ This is a unique opportunity to contribute to life-saving therapies while advancing your career in the exciting world of biopharmaceutical manufacturing. If you meet the qualifications and are passionate about making a difference, we encourage you to apply inside the job description!


๐Ÿ“ฉ Submit your updated resume today to be considered for this impactful role.


โœจ Together, letโ€™s make a difference!


Thank you. We will be in contact soon.

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