Team Lead, Quality Control (In-Process Controls & Validations) at Arrowhead Pharmaceuticals

Verona, Wisconsin, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Dec, 25

Salary

100000.0

Posted On

20 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Leadership, Analytical Techniques, cGMP Requirements, ICH Guidelines, Analytical Instrumentation, Method Validation, Data Interpretation, Training, Mentoring, Collaboration, Problem Solving, Technical Documentation, Communication, Workflow Management, Project Management, Quality Control

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 falls within the Quality Control structure, under the Quality Assurance Organization. The Team Leader, IPCs & Validations will manage chemists and help to support the analytical testing of pharmaceutical in process manufacturing samples, and validation (analytical methods and computer systems) activities for drug substances and drug products while carrying out a supervisory function. They will work cross-functionally to identity and resolve any issues that arise. They will have the opportunity to hold leadership functions for project support personnel. The Team Leader IPCs & Validations will manage, and support testing required. The Team Leader is expected to be proficient in analytical techniques and capable of making independent scientific decisions. They will assist in the drafting and maintenance of study documents (testing directives, methods, reports) and manage deadlines. The position also requires the ability to lead and mentor chemists who are new to the industry. This position reports to QC Laboratory Senior Management. Responsibilities Management Provide leadership and guidance to a team of QC chemists, ensuring their professional growth and development. Set clear performance expectations, provide regular feedback, and conduct performance evaluations. Foster a collaborative and inclusive work environment that encourages teamwork, creativity, and innovation. Attend and contribute to regular leadership meetings between cross-functional departments. Scientific/Laboratory Fully knowledgeable of cGMP requirements and ICH guidelines Frequently works independently to meet project timelines and deliverables with minimal supervision to no supervision Collaborates with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols Proficient with various analytical instrumentation theory and practice Executes training requirements for assigned SOPs and participates in department specific training Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in analyst training on instrumentation as Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization Works closely with QA, Analytical Development and/or Manufacturing personnel for efficient project execution and timely/accurate deliverables Trains and mentors both entry chemists as well as mid-level chemists Ability to track/trend data and interpret degrative changes to the product on stability Leads and assists in scientific technical discussions and brainstorming sessions Identifies and troubleshoots analytical method issues with instrumentation, general chemistry, test methodology and sample product Communicates laboratory testing issues or challenges to senior laboratory management Maintains a clear, concise, and accurate notebook Drafts technical documents such as OOS/atypical investigations, deviations and CAPAs Possesses clear written and verbal communication skills Embraces cGMP and ICH requirements for all associated work Calibration, maintenance, and troubleshooting of analytical equipment in collaboration with metrology Routinely makes sound, scientific decisions and serves as a back-up to Senior Laboratory Management Other Skills and Abilities Must be able to work with people at various levels of the organization. Must have basic knowledge of computers and PC's. Ability to use windows-based software including MS Office and chromatography data collection software. Must be able to solve practical problems. Must be able to interpret a variety of instructions furnished in written, oral, diagram or schedule form. Must be able to perform complex mathematical calculations, compute ratios, rate, and percent. Must be able to draw and interpret graphs and charts. Ability to read, analyze and interpret SOPs, test methods, procedural guides and associated technical documents. Ability to write in a clear and concise manner. Ability to effectively present/communicate information and respond to questions from management, peers and colleagues. Requirements: Master's in Chemistry (or related field) with 5+ years relevant laboratory experience Bachelor's in Chemistry (or related field) with 7+ years of relevant laboratory experience Fully knowledgeable of cGMP and ICH laboratory requirements and operations Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices Wisconsin pay range $85,000—$100,000 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 Team Leader will manage chemists and support analytical testing of pharmaceutical in-process manufacturing samples and validation activities. They will work cross-functionally to identify and resolve issues while mentoring new and mid-level chemists.