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Associate Scientist
2 weeks ago
Job Family:Biologist (Digital)Travel Required:Up to 25%Clearance Required:Ability to Obtain Public TrustWhat You Will Do:Develop downstream (purification) processes, under the oversight of a project lead scientist, for recombinant proteins, virus vaccines, and virus-like particles (VLP) that may be used as clinical candidates.Work collaboratively within the purification group to design, develop and optimize chromatography and filtration step unit operations to support process development of clinical trial vaccine candidates and mAb products.Purify research-phase recombinant proteins, virus vaccines and/or virus-like particles in support of other groups or external collaborators.Work to prepare necessary materials (buffers, packed columns, etc.) in support of downstream process activities.Utilize novel process monitoring technologies (e.g. PatFix or other point-of-use analytics) towards optimizing downstream process unit operations.Execute automated systems (e.g. Tecan Bioprocess Liquid Handlers, or similar) to perform parallel purification processes or development studies.Perform scale-down model qualification runs and associated studies to support viral clearance validation work.Support technology transfer of processes to Lab’s Pilot Plant for manufacture of clinical product through document generation and on-site support.What You Will Need:Bachelor’s degree in Bioengineering, Chemical Engineering, Biochemistry, or a related discipline is required.Minimum of (FOUR) 4 years of experience in recombinant protein purification development and/or related manufacturing of GMP clinical-phase products is required.Demonstrated knowledge of maintaining accurate and detailed records.Must be a team player who can effectively work with members from cross-functional departments.Strong oral and written communication skills.Familiarity with computer software including word processing and data evaluation.Must be able to OBTAIN and MAINTAIN a Federal or DoD "PUBLIC TRUST"; candidates must obtain approved adjudication of their PUBLIC TRUST prior to onboarding with Guidehouse. Candidates with an ACTIVE PUBLIC TRUST or SUITABILITY are preferred.What Would Be Nice To Have:Write and review technical protocols and reports.Analyze and compile data, present at various group/department meetings.Experience in a clinical research environment.The annual salary range for this position is $85,000.00-$141,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs.What We Offer:Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.Benefits include:Medical, Rx, Dental & Vision InsurancePersonal and Family Sick Time & Company Paid HolidaysParental Leave401(k) Retirement PlanGroup Term Life and Travel AssistanceVoluntary Life and AD&D InsuranceHealth Savings Account, Health Care & Dependent Care Flexible Spending AccountsTransit and Parking Commuter BenefitsShort-Term & Long-Term DisabilityTuition Reimbursement, Personal Development, Certifications & Learning OpportunitiesEmployee Referral ProgramCorporate Sponsored Events & Community OutreachEmployee Assistance ProgramSupplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)Position may be eligible for a discretionary variable incentive bonus
