Piper Companies
Overview
Piper Companies is seeking a highly motivated and technically skilled
MS&T Scientist
to support the development, scale-up, and technology transfer of biopharmaceutical manufacturing processes for a well-established biopharmaceutical organization out of Frederick, MD. Responsibilities
Provide technical support for upstream and/or downstream manufacturing operations Analyze process data to identify trends, deviations, and opportunities for improvement Lead investigations into process deviations and implement CAPAs Support or lead technology transfer activities from development to clinical or commercial manufacturing sites Participate in process scale-up studies and validation campaigns Collaborate with cross-functional teams to ensure successful execution of process performance qualification (PPQ) and continued process verification (CPV) Prepare technical reports, presentations, and documentation for internal and regulatory use Qualifications
4+ years of experience working in upstream or downstream manufacturing operations Experience working in a GMP (Good Manufacturing Environment) MS&T experience highly desired for this role Strong understanding of biologics manufacturing processes including mammalian cell culture, purification, formulation scale up processes Experience with monoclonal antibodies and cell/gene therapies preferred Tech transfer across manufacturing sites would be ideal experience for candidate Bachelor’s degree in life science related field Compensation
Salary: Between $80,000 - $115,000 based on years of relevant experience Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO (Paid Time Off), Paid Holidays, Sick Leave as required by law This job opens for applications on 10/10/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords
Manufacturing, biopharmaceutical, MS&T, manufacturing science and technology, manufacturing science & technology, bioprocessing, upstream, downstream, cell culture, fermentation, mammalian, scale up, scale-up, protein purification, chromatography, filtration, process development, process scale-up, process optimization, process characterization, validation, PPQ, CPV, tech transfer, analytical method development, method development, analytical, formulation development, PAT, process analytical technology, qbd, quality by design, aseptic processing, laboratory, GMP, good manufacturing practice, biotechnology, biotech, single-use, bioreactor, CAPA, deviation, QA, quality assurance, ICH, FDA, EMA, change control, corrective and preventative actions, batch record, IND, BLA, NDA, regulatory, technical writing, LIMS, Python, TFF, tangential flow filtration, depth filtration, filtration, centrifugation, affinity, ion exchange, harvesting, ultrafiltration, diafiltration, UF/DF, viral clearance, column packing, scale-down modeling, HPLC, SDS-page, ELISA, DOE, design of experiment, CHO, microbial fermentation, HEK293, media preparation, single-use, stainless steel, seed train, pH, nutrient feeding, CPP, critical process parameter, CQA, critical quality attributes, GLP, good laboratory practice, manufacturing specialist, manufacturing associate, bioprocess associate, process development associate #LI-BN1 #LI-ONSITE
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Piper Companies is seeking a highly motivated and technically skilled
MS&T Scientist
to support the development, scale-up, and technology transfer of biopharmaceutical manufacturing processes for a well-established biopharmaceutical organization out of Frederick, MD. Responsibilities
Provide technical support for upstream and/or downstream manufacturing operations Analyze process data to identify trends, deviations, and opportunities for improvement Lead investigations into process deviations and implement CAPAs Support or lead technology transfer activities from development to clinical or commercial manufacturing sites Participate in process scale-up studies and validation campaigns Collaborate with cross-functional teams to ensure successful execution of process performance qualification (PPQ) and continued process verification (CPV) Prepare technical reports, presentations, and documentation for internal and regulatory use Qualifications
4+ years of experience working in upstream or downstream manufacturing operations Experience working in a GMP (Good Manufacturing Environment) MS&T experience highly desired for this role Strong understanding of biologics manufacturing processes including mammalian cell culture, purification, formulation scale up processes Experience with monoclonal antibodies and cell/gene therapies preferred Tech transfer across manufacturing sites would be ideal experience for candidate Bachelor’s degree in life science related field Compensation
Salary: Between $80,000 - $115,000 based on years of relevant experience Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO (Paid Time Off), Paid Holidays, Sick Leave as required by law This job opens for applications on 10/10/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords
Manufacturing, biopharmaceutical, MS&T, manufacturing science and technology, manufacturing science & technology, bioprocessing, upstream, downstream, cell culture, fermentation, mammalian, scale up, scale-up, protein purification, chromatography, filtration, process development, process scale-up, process optimization, process characterization, validation, PPQ, CPV, tech transfer, analytical method development, method development, analytical, formulation development, PAT, process analytical technology, qbd, quality by design, aseptic processing, laboratory, GMP, good manufacturing practice, biotechnology, biotech, single-use, bioreactor, CAPA, deviation, QA, quality assurance, ICH, FDA, EMA, change control, corrective and preventative actions, batch record, IND, BLA, NDA, regulatory, technical writing, LIMS, Python, TFF, tangential flow filtration, depth filtration, filtration, centrifugation, affinity, ion exchange, harvesting, ultrafiltration, diafiltration, UF/DF, viral clearance, column packing, scale-down modeling, HPLC, SDS-page, ELISA, DOE, design of experiment, CHO, microbial fermentation, HEK293, media preparation, single-use, stainless steel, seed train, pH, nutrient feeding, CPP, critical process parameter, CQA, critical quality attributes, GLP, good laboratory practice, manufacturing specialist, manufacturing associate, bioprocess associate, process development associate #LI-BN1 #LI-ONSITE
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