What are the responsibilities and job description for the Senior Scientist / Scientist, Quality Control Analytical Development position at JMD Technologies Inc.?
Title: Senior Scientist / Scientist, Quality Control Analytical Development
Location: Greater Milford Area, MA (Onsite)
Employment Type: Contract (6 months)
Status: Accepting Candidates
About the role
This position supports QC Analytical Development through analytical method qualification, validation, and assay execution for biologic drug substances. The role partners closely with development and QC teams to advance methods into GMP testing environments.
Key Responsibilities
• Perform analytical method qualification and validation for biologics and process-related impurities.
• Execute ELISA, qPCR, and potency assays supporting method lifecycle activities.
• Support method development, transfer, and technology transfer into QC laboratories.
• Prepare, review, and revise technical protocols, reports, and SOPs.
• Collaborate cross-functionally with QC and development teams to ensure method readiness.
• Provide training and technical guidance to team members when needed.
Qualifications
• Bachelor’s degree with 8 years, or Master’s with 5 years in Chemistry, Biology, or related field.
• Hands-on experience with ELISA, qPCR, immunochemistry, and biologics analytical characterization.
• Strong understanding of cGMP, pharmaceutical analytical development, and method lifecycle.
• Experience with SoftMax and plate-based analytical systems.
• Background with biologics, monoclonal antibodies, drug substances/products preferred.
• Excellent documentation, communication, and organizational skills.
Compensation (MA Pay Transparency):
• Estimated hourly range (Senior Scientist): $55–$65/hr (W-2).
• Final rate within this range will be based on skills, experience, and interview results.
Salary : $55 - $65