Associate Manufacturing Scientist III (3rd shift) at Arrowhead Pharmaceuticals

Verona, Wisconsin, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Dec, 25

Salary

90000.0

Posted On

20 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Oligonucleotide Synthesis, GMP Compliance, Process Improvement, Analytical Thinking, Team Collaboration, Documentation, Equipment Operation, Training, Safety Protocols, Batch Record Preparation, LCMS Analysis, Vendor Communication, Raw Material Tracking, Problem Solving, Critical Thinking

Industry

Biotechnology Research

Description

Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position This position will involve assisting in the synthesis and subsequent purification steps of large scale oligonucleotides. The operator must comply with GLP/GMP protocols and be able to follow all association SOPs and work instructions when performing and documenting operations. This is a 3rd shift position, working four 10-hour shifts Monday - Thursday. This role is eligible for a 15% shift differential. Responsibilities Prepare batch records, SOPs, and work instructions to detail Document all operations in batch records and notebooks Experience in investigating and closing deviations Ability to identify, design, and implement process improvements Comply with GMP protocols Operate large scale oligonucleotide manufacturing equipment (i.e. oligonucleotide synthesizer, purification skid, tangential flow filtration system, lyophilizer, ChemGlass reactors, pH/conductivity meters, peristaltic pumps, ) Lead and provide support to other chemists within the CMC group during synthesis and purification of oligonucleotides including: Reagent solution preparation Mobile phase preparation Column Packing Fraction collection Develop and optimize test methods for oligonucleotide/intermediate analysis via LCMS Assist in scale up/process development from small/mid-scale chemistry Contact vendors for purchasing manufacturing equipment/performing routine maintenance and repair, and assist with FATs for equipment as needed Maintain a clean work space Maintain safety by wearing required personal protective equipment Maintain safety by wearing required personal protective equipment Track and update raw material usage in D365 ERP software Act as production campaign lead Assist with new personnel training Address and resolve production challenges proactively, utilizing analytical and critical thinking skills Requirements: Bachelors degree in a scientific field 5-10 years experience in a similar position Experience working in a GMP setting and controlled documentation Ability to move and lift up to 50 pounds Good verbal and written communication skills Ability to work in a team environment Ability to pay attention to detail Wisconsin pay range $78,000—$90,000 USD Arrowhead provides competitive salaries and an excellent benefit package. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Responsibilities

The position involves assisting in the synthesis and purification of large scale oligonucleotides while complying with GLP/GMP protocols. The role includes documenting operations, leading production campaigns, and supporting other chemists in the CMC group.