ZipRecruiter
Lead Purification Scientist - Bioprocess Development
ZipRecruiter, Framingham, Massachusetts, us, 01704
Overview
The Lead Purification Scientist will lead a team of scientists and analysts in executing small-scale purification studies to support biopharmaceutical manufacturing processes. This role combines hands-on technical expertise with leadership responsibilities, ensuring high-quality data, documentation, and cross-functional collaboration. The Group Leader will drive innovation, manage project timelines, and support technology transfer activities. Key Responsibilities
Technical Expertise: Design and execute small-scale purification studies using chromatography, ultrafiltration/diafiltration (UF/DF), tangential flow filtration (TFF), and sterile/depth filtration techniques. Operate and troubleshoot chromatography systems (e.g., AKTA) and associated software (Unicorn) for experimental purification runs. Perform essential lab support tasks, including solution preparation, sample submission, and equipment calibration. Analyze complex datasets using statistical tools and author detailed technical reports to support study conclusions. Present findings in cross-functional meetings and actively contribute to scientific and strategic discussions. Lead purification efforts for assigned projects, ensuring thorough planning, execution, and documentation. Collaborate with cross-disciplinary teams to align lab activities with broader project goals. Maintain compliance with GxP standards, GHS policies, and internal protocols. Manage multiple concurrent projects, prioritize tasks effectively, and communicate progress across teams. Leadership & Team Development: Supervise a team of analysts, ensuring timely and high-quality execution of laboratory work. Participate in recruitment efforts, including candidate interviews and hiring decisions. Lead onboarding and training initiatives for new team members; provide ongoing mentorship and skill development. Conduct performance evaluations and deliver constructive feedback to support professional growth. Monitor team workload and optimize resource allocation to meet project timelines. Engage in leadership development and foster a culture of continuous improvement and scientific excellence. Qualifications
Education & Experience: Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related field with 3+ years of relevant industry experience, or Master’s degree with 1+ years of experience. Hands-on experience with downstream purification processes in pilot-scale or R&D environments. Familiarity with AKTA systems and Unicorn software. Technical Skills: Strong documentation and organizational capabilities. Proficient in lab equipment operation and data interpretation. Experience troubleshooting downstream processes such as chromatography, UF/DF, and filtration. Exposure to scale-up, tech transfer, and GMP manufacturing support. Knowledge of upstream processing is a plus. Experience with tools such as Solo VPE, JMP, Viper, BioSMB, PALL System Software, Pendotech, and Microsoft Office. Additional Requirements: Excellent communication and time management skills. Comfortable working in both collaborative (60%) and independent (40%) settings. Physically capable of lifting/pushing up to 75 lbs, standing for extended periods, and working on platforms/ladders. Must be authorized to work in the United States indefinitely without restriction or sponsorship. Benefits
Medical Coverage: Comprehensive medical insurance options Dental & Vision: Full dental and vision coverage available Life & Insurance: Employer-sponsored plans Retirement: 401(k) plan with company match Paid Time Off: Vacation days, paid holidays, and additional PTO options Compensation: $42.00 - 47.00 per hour Annual equivalent: $87,360–$97,760 Note:
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
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The Lead Purification Scientist will lead a team of scientists and analysts in executing small-scale purification studies to support biopharmaceutical manufacturing processes. This role combines hands-on technical expertise with leadership responsibilities, ensuring high-quality data, documentation, and cross-functional collaboration. The Group Leader will drive innovation, manage project timelines, and support technology transfer activities. Key Responsibilities
Technical Expertise: Design and execute small-scale purification studies using chromatography, ultrafiltration/diafiltration (UF/DF), tangential flow filtration (TFF), and sterile/depth filtration techniques. Operate and troubleshoot chromatography systems (e.g., AKTA) and associated software (Unicorn) for experimental purification runs. Perform essential lab support tasks, including solution preparation, sample submission, and equipment calibration. Analyze complex datasets using statistical tools and author detailed technical reports to support study conclusions. Present findings in cross-functional meetings and actively contribute to scientific and strategic discussions. Lead purification efforts for assigned projects, ensuring thorough planning, execution, and documentation. Collaborate with cross-disciplinary teams to align lab activities with broader project goals. Maintain compliance with GxP standards, GHS policies, and internal protocols. Manage multiple concurrent projects, prioritize tasks effectively, and communicate progress across teams. Leadership & Team Development: Supervise a team of analysts, ensuring timely and high-quality execution of laboratory work. Participate in recruitment efforts, including candidate interviews and hiring decisions. Lead onboarding and training initiatives for new team members; provide ongoing mentorship and skill development. Conduct performance evaluations and deliver constructive feedback to support professional growth. Monitor team workload and optimize resource allocation to meet project timelines. Engage in leadership development and foster a culture of continuous improvement and scientific excellence. Qualifications
Education & Experience: Bachelor’s degree in chemistry, biology, pharmacy, engineering, or related field with 3+ years of relevant industry experience, or Master’s degree with 1+ years of experience. Hands-on experience with downstream purification processes in pilot-scale or R&D environments. Familiarity with AKTA systems and Unicorn software. Technical Skills: Strong documentation and organizational capabilities. Proficient in lab equipment operation and data interpretation. Experience troubleshooting downstream processes such as chromatography, UF/DF, and filtration. Exposure to scale-up, tech transfer, and GMP manufacturing support. Knowledge of upstream processing is a plus. Experience with tools such as Solo VPE, JMP, Viper, BioSMB, PALL System Software, Pendotech, and Microsoft Office. Additional Requirements: Excellent communication and time management skills. Comfortable working in both collaborative (60%) and independent (40%) settings. Physically capable of lifting/pushing up to 75 lbs, standing for extended periods, and working on platforms/ladders. Must be authorized to work in the United States indefinitely without restriction or sponsorship. Benefits
Medical Coverage: Comprehensive medical insurance options Dental & Vision: Full dental and vision coverage available Life & Insurance: Employer-sponsored plans Retirement: 401(k) plan with company match Paid Time Off: Vacation days, paid holidays, and additional PTO options Compensation: $42.00 - 47.00 per hour Annual equivalent: $87,360–$97,760 Note:
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
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