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Remote Good Molecules Jobs in Wisconsin (NOW HIRING)

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Remote Good Molecules information

What is a remote Good Molecules job?

Remote Good Molecules jobs refer to employment opportunities with Good Molecules, a skincare brand, that allow employees to work from locations outside of the company's physical offices. These roles may include positions in customer service, marketing, research, product development, or other functions that can be performed remotely. Working remotely for Good Molecules typically requires strong communication skills, self-motivation, and the ability to collaborate with team members online. Benefits may include flexible working hours and the ability to maintain a better work-life balance.

What skills and qualifications are needed to thrive as a remote Customer Service Representative at Good Molecules?

To thrive as a Remote Customer Service Representative at Good Molecules, you need excellent communication abilities, problem-solving skills, and prior experience in customer support or a related field. Familiarity with customer relationship management (CRM) tools, help desk software, and basic office applications is typically required. Strong empathy, patience, and time management enable representatives to connect with customers and resolve issues efficiently while working independently. These skills ensure high-quality service, customer satisfaction, and effective remote collaboration in a fast-paced e-commerce environment.

How does working remotely at Good Molecules affect daily communication and collaboration with colleagues?

As a remote team member at Good Molecules, you'll find that daily communication relies heavily on digital tools such as Slack, Zoom, and project management platforms. Team members often participate in regular virtual meetings to ensure alignment and maintain a collaborative work environment. You'll be expected to proactively communicate your progress, ask questions, and share feedback to foster transparency. While remote work offers flexibility, it also requires strong self-discipline and time management to meet deadlines and contribute effectively to team goals.

What is the difference between Remote Good Molecules vs Remote Cosmetic Chemist?

AspectRemote Good MoleculesRemote Cosmetic Chemist
CredentialsTypically requires a background in chemistry or cosmetic scienceRequires a degree in chemistry, chemical engineering, or related field
Work EnvironmentRemote, often in product development or formulationRemote or hybrid, focused on formulation and product testing
Industry UsageSkincare, beauty, and cosmetic product companiesCosmetic and personal care product companies
Search & Comparison IntentPeople comparing roles in skincare product formulationProfessionals seeking formulation or development roles in cosmetics

Remote Good Molecules and Remote Cosmetic Chemist roles both involve formulation and product development in the beauty industry. While they share similar credentials and work environments, the term 'Remote Good Molecules' often refers to roles within the skincare brand itself, whereas 'Remote Cosmetic Chemist' is a broader industry term for professionals working on cosmetic formulations across various companies.

What are the most commonly searched types of Good Molecules jobs in Wisconsin?

The most popular types of Good Molecules jobs in Wisconsin are:

What are popular job titles related to Remote Good Molecules jobs in Wisconsin?

For Remote Good Molecules jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Remote Good Molecules jobs in Wisconsin look for?

The top searched job categories for Remote Good Molecules jobs in Wisconsin are:

What cities in Wisconsin are hiring for Remote Good Molecules jobs?

Cities in Wisconsin with the most Remote Good Molecules job openings:

Remote Good Molecules jobs near you
Infographic showing various Remote Good Molecules job openings in Wisconsin as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 4% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Senior QA Specialist - Supplier Quality

Arrowhead Pharmaceuticals

Madison, WI • On-site, Remote

$83K - $114K/yr

Full-time

Posted 12 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial 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

The Senior Specialist, Quality Agreements is a member of the Supplier Quality team and is responsible for the development, negotiation, execution, and lifecycle management of Quality Agreements (i.e. QTAs, QAAs, etc.) with raw material suppliers, contract manufacturing organizations (CMOs/CDMOs), contract testing laboratories, distributors, and other external partners in the pharmaceutical supply chain supporting clinical and commercial programs at Arrowhead Pharmaceuticals.

This role ensures that quality and compliance responsibilities are clearly defined, aligned with applicable regulatory requirements (FDA, EMA, ICH, ISO), and fully integrated with the broader Supplier Quality Management program — including supplier qualification, risk classification, performance monitoring, and periodic review. The ideal candidate combines strong technical writing skills, GMP/regulatory knowledge, and cross-functional collaboration experience to ensure every supplier and partner relationship has clear, current, and enforceable quality terms.

Responsibilities

  • Draft, review, revise, and finalize Quality Agreements with raw material suppliers, CMOs/CDMOs, contract testing laboratories, distributors, and other GMP-relevant external partners, in collaboration with Legal, Procurement, Regulatory Affairs, and Operations.
  • Serve as the Supplier Quality team's primary point of contact for Quality Agreement negotiations, ensuring roles and responsibilities are clearly delineated (e.g., batch/lot release, deviation and CAPA ownership, change control notification, complaint handling, audit and inspection rights, sub-tier supplier oversight).
  • Own and maintain the master Quality Agreement tracker/inventory within the Supplier Quality program, including renewal dates, amendments, expiration alerts, and linkage to supplier risk tier.
  • Ensure Quality Agreements align with current Good Manufacturing Practice (cGMP), applicable global regulatory requirements, and internal quality policies/SOPs.
  • Integrate Quality Agreement requirements into the full Supplier Quality Management lifecycle, including new supplier qualification, risk classification, periodic/annual supplier review, and supplier scorecards.
  • Collaborate with Supplier Quality team members to ensure Quality Agreement terms are reflected in supplier audit scope and are verified during on-site or remote assessments.
  • Coordinate cross-functional review and approval workflows, drive agreements to closure within established timelines and escalate stalled negotiations as needed.
  • Identify gaps, inconsistencies, or outdated terms in existing agreements (e.g., following organizational, regulatory, or product changes) and lead remediation and re-negotiation efforts.
  • Support internal and external audits and regulatory inspections by providing Quality Agreement documentation and responding to related findings or observations.
  • Track and report Supplier Quality Agreement metrics to Supplier Quality leadership.
  • Contribute to continuous improvement of Quality Agreement templates, workflows, and the associated Supplier Quality Management System (QMS) procedures, as well as overall QMS programs and procedures.
  • Assist with QA duties as needed.

Requirements

  • Bachelor's degree in a scientific, technical, or related field (e.g., Life Sciences, Chemistry, Pharmacy, Engineering) or equivalent experience
  • Minimum of 8 years of quality assurance experience in a pharmaceutical or biotechnology quality, with 4+ years in supplier quality.
  • Demonstrated experience drafting and/or negotiating Quality Agreements with suppliers, CMOs/CDMOs, or contract testing laboratories.
  • Solid working knowledge of cGMP requirements and global regulatory frameworks (FDA 21 CFR Parts 210/211, EU GMP Annex 16, ICH Q7/Q9/Q10).
  • Excellent written and verbal communication skills, with strong attention to detail and technical writing ability.
  • Proven ability to manage multiple priorities and stakeholders in a cross-functional, matrixed environment.
  • Proficiency with document management/QMS platforms and standard office software.

Preferred

  • Direct experience as part of a Supplier Quality or Vendor Management team, including supplier audits or assessments.
  • Familiarity with API, excipient, or component supplier quality requirements.
  • Strong negotiation and stakeholder-management skills
  • Organized, with strong follow-through on deadlines and deliverables
  • Excellent interpersonal, verbal, and written communication skills.
  • Ability to consistently communicate with external parties in a professional manner.
  • Ability to work independently with minimal supervision as well as manage priorities within a face paced environment.
Wisconsin pay range
$90,000—$110,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.   

Candidates must have current, valid authorization to work in the country where this role is located.

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