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KS
Kelly Services
Senior Associate
Career Insights for Technical Sales Specialist
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Based on Michigan data
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What they do
A Technical Sales Specialist sells technology products or services for a company and provides specialized technical assistance for customers. May assist with product installation, training for users, maintenance and repairs or upgrades. May travel within a sales district or region to meet with business customers and maintain technology products or service contracts.
$95,357 / year median in Michigan
-15% projected decline
Job Description
Senior Associate Apply Now Applied To save a job sign in or get started
Job ID:
10350298 Posted today Back Troy, MI, US Electronic Assembly High School or equivalent Full Time, Temporary $36.54- 37.98/hour Experienced (Non-Manager) On-site Biotechnology/Pharmaceuticals Third Shift (Night) Troy, MI, US $36.54
- 37.98/hour Experienced (Non-Manager) Full Time, Temporary Biotechnology/Pharmaceuticals On-site Electronic Assembly High School or equivalent Third Shift (Night) Apply Now Applied Job details Senior Associate
Biomanufacturing, Downstream/mRNA Location:
Madison, WI (100% On-Site)Work Schedule:
10:00pm-8:00am (Sunday-Wednesday or Wednesday-Saturday)Compensation:
$76,000- 79,000/year (base hourly equivalent: $36.54
- 37.
Opportunity:
Join a leading global Contract Development and Manufacturing Organization (CDMO) in a cutting-edge 263,000 sq. ft. GMP facility specializing in mammalian cell line engineering, scalable biomanufacturing, and integrated analytical services.Position Summary:
The Senior Associate- Biomanufacturing, Downstream/mRNA provides advanced process and technical leadership for biopharmaceutical manufacturing within a clean room environment, focusing on mRNA production and downstream processing activities.
Key Responsibilities:
Execute and troubleshoot advanced downstream mRNA purification activities, including IVT reactions, chromatography, TFF, viral filtration, bulk drug substance filling, and column packing/qualification. Follow Batch Production Records (BPRs) and Standard Operating Procedures (SOPs) in full compliance with cGMPs, emphasizing right-first-time execution. Document all activities according to Good Documentation Practices (GDPs) in BPRs, forms, and quality documents. Identify and report procedure deviations; proactively recommend safety, quality, and efficiency improvements. Participate in and help lead Continuous Improvement (CI) activities, including "Just Do It" projects. Mentor junior team members and support onboarding; may serve as Certified Trainer. Interact with clients during Person In Plant (PIP) or virtual sessions to provide batch updates. Participate in shift huddles and lead shift exchanges. Perform general cleanroom housekeeping and maintain 5S standards. Other duties as assigned.Requirements:
High School Diploma or equivalent with at least 7 years of relevant experience; OR Associate's/Bachelor's degree in scientific or related discipline with 3+ years of experience; OR Master's degree in STEM with 1+ year of experience. GMP manufacturing experience preferred. Familiarity with Microsoft Word, Excel, and other business software systems required. Preferred experience with TrackWise, ComplianceWire, JD Edwards, DeltaV, and Unicorn. Ability to work in a cleanroom and meet outlined physical requirements.Benefits:
Clearly defined career path with ongoing feedback and annual reviews Diverse and inclusive work culture Career growth opportunities 152 hours PTO + 8 paid holidays Generous 401(k) match Medical, dental, and vision benefits Tuition reimbursement 10350298 Share this job Copied url To save a job sign in or get started To apply for this job email your details to I want more jobs like this in my inbox.GET JOB ALERTS
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