Research Associate II (Onsite) at Partner Therapeutics

, Washington, United States -

Full Time

Start Date

Immediate

Expiry Date

01 Jul, 26

Salary

92500.0

Posted On

02 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Downstream Purification Processes, Semi-Preparative Chromatography, Membrane Technology, Low-Pressure Chromatography, Protein Analytical Methods, Data Analysis, Project Management, Communication Skills, Technical Support, Process Development, Continuous Process Improvement, Collaboration, Laboratory Methods, Experimental Design, Statistical Analysis, Technology Transfer

Industry

Biotechnology Research

Description

The Downstream (purification) Process Science team is a group of Scientists and Subject Matter Experts who specialize in the development, optimization, remediation, and transfer of the downstream processes used in cGMP commercial manufacturing of drug substance. This position is primarily a lab-based role which requires hands-on execution of downstream development, optimization and characterization experiments using small-scale chromatography models, along with analysis and interpretation of experimental data. PRIMARY RESPONSIBILITIES Supports and contributes to laboratory experiments related to the development, optimization, characterization and scale-up of downstream protein purification processes. Executes assigned experiments that support process development activities and project goals using semi-preparative chromatography, membrane technology and low-pressure chromatography (ion exchange, affinity, size exclusion). Quantify and characterize protein targets and impurities using typical protein analytical methods (HPLC, DSD-PAGE, western blotting, UV-VIS spectrophotometry, etc.) Analyze data, interpret results, form conclusions, and assist in planning future studies in a collaborative environment. Provides downstream technical support for cGMP manufacturing operations by contributing insights to solve routine technical issues. Provides support for technology transfer of downstream processes to a cGMP facility. Actively participate in idea generation including identification and optimization of alternative laboratory methods and/or equipment in support of continuous process improvement and process life cycle management objectives. Communicates work through oral presentations and written documentation, including technical reports. Author/review development protocols, development reports, SOP’s and batch records Uses professional concepts to complete data entry, data analysis and maintenance of accurate experimental records. Collaborates with key partners (upstream scientists, analytical scientists, and manufacturing and quality colleagues). KNOWLEDGE, SKILLS, ABILITIES Required: Working experience with typical downstream purification processes, including semi-preparative chromatography, membrane technology (TFF) and low-pressure chromatography (ion exchange, affinity, size exclusion). Working experience with fundamental protein analytical methods Demonstrated strong organizational, interpersonal and project management skills. Ability to work independently and provide training to junior team members. Ability to independently make decisions based on data, scientific knowledge, and sound judgement. Excellent communication skills both written and oral. Maintain a safe work environment in accordance with policies, procedures, and regulations. Preferred: Experience with peptide mapping and LC/MS desirable Understanding of ICH and FDA guidelines Working knowledge of statistical analysis techniques (standard deviation, t-test, p-value), Design of Experiments (DOE), and associated software (JMP, etc.). EXPERIENCE & EDUCATION Required: B.S. in a scientific or engineering discipline and a minimum of 2+ years related experience; or a M.S. and 0-2 years. Knowledge of scientific principles and concepts. Preferred: B.S. or M.S. in Bioengineering, Chemical Engineering and Chemistry. PTx is committed to the principles of competitive and pay equity for all of our Partners. The current pay range for this position is $74,000 - $92,500: Offers are made within the base pay range applicable at the time. Your salary will vary depending on several factors including your qualifications and experience. In addition to medical, dental, vision, FSA/DCA, HRA, disability, and life insurance coverage, all full-time, regular Partners enjoy a casual, and Hybrid or Remote workplace program for many roles. We offer a terrific compensation/benefits/perks package which includes an annual cash bonus, 401k matching, free parking or Seattle-area ORCA pass, tuition assistance, plus rewards for achievement and contribution. To support a healthy work-life balance we also provide a gym subsidy, wellness participation programs, and a generous vacation, sick, and holiday paid time off program in addition to a paid shutdown between the Christmas and New Year’s holidays. Partner Therapeutics is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, age, national origin, veteran status, marital status, sexual orientation, gender identity, disability or any other category prohibited by local, state, or federal law. This policy applies to all aspects of employment, including recruitment, placement, promotion, transfer, demotion, compensation, benefits, social and recreational activities, and termination.

Responsibilities

The Research Associate II will support laboratory experiments related to the development and optimization of downstream protein purification processes. They will analyze data, interpret results, and assist in planning future studies while providing technical support for cGMP manufacturing operations.