Partner Therapeutics

Research Associate II (Onsite)

Partner Therapeutics  •  $74k - $93k/yr  •  Lynnwood, WA (Hybrid)  •  2 days ago
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Job Description

Location: Lynnwood,Washington,United States

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.

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Partner Therapeutics

About Partner Therapeutics

WE'RE ALL IN FOR FIGHT AGAINST CANCER

Partner Therapeutics is devoted to developing and commercializing cancer medicines and combination therapies that can make a meaningful difference in the lives of cancer patients. We are united in our passion for improving the treatment of cancer and our desire to make a meaningful contribution to outcomes.

THE PATIENT IS NUMBER ONE

We believe that being a cancer company begins and ends with the patient. We strive to support patient needs throughout their treatment journey to help them make the treatment choices that are right for them and their loved ones.

FIGHTING CANCER IS TEAM SPORT

We believe that cancer is a complex, dynamic disease that requires a multi-faceted, multi-disciplinary approach to tackle. We believe in teamwork at each stage of a therapy’s development, and seek to build teams of experts, both internally and externally, that cover the breadth and depth of the complex problem that is cancer.

We work with leading companies and investigators to ensure that our products are tested in the best settings, and in combination with highest potential regimens to maximize benefit to patients and to advance the understanding of cancer treatment.

We seek to engage all members of the cancer treatment team as well as thought-leading physicians and patient advocacy organizations to ensure that clear, complete and balanced information about our products is proactively communicated and readily available. We work to support the extraordinary dedication of the medical teams that represent the front lines in the war on cancer.

OUTCOMES ARE OUR YARDSTICK

We believe that innovation is not enough. In the challenging world of today’s healthcare climate, we strive to develop and assess our products based on the real-world impact they have in improving the quality and duration of our patients’ lives. We measure our success in the birthdays, anniversaries and other important life moments that our patients are able to enjoy.

Industry
Biotech & Life Sciences
Company Size
51-200 employees
Headquarters
Lexington, Massachusetts
Year Founded
2017
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