The Goodkind Co. (Manufacturing)

End-to-end contract manufacturer for personal care

Director of Compounding

Machine & Process OperationConfirmed live in the last 24 hours

Full-timeRound Rock, TX, USANo salary listed

About the Job

Requirements

A bachelor's degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences, or a related field, or equivalent experience.
At least 10 years of experience in cosmetic, personal care, over-the-counter, or pharmaceutical batch manufacturing.
At least 5 years of management experience leading a compounding or manufacturing function with multiple direct reports.
Hands-on commercial-scale experience with hot-pour or anhydrous stick products and emulsions, including process sensitivities of waxes, fatty alcohols, and glycol-based systems.
Working knowledge of current Good Manufacturing Practices (21 CFR 210/211) and ISO 22716, with experience hosting or supporting FDA and customer audits.
A proven record of improving yield, right-first-time performance, and schedule attainment in a contract manufacturing or multi-SKU environment.
Experience with scale-up and technology transfer from research and development to production.
Ability to read and interpret formulas, batch records, certificates of analysis, and specifications, and troubleshoot batches on the production floor.
Experience in a fast-paced, high-volume organization requiring quick decision-making and effective communication.
Ability to operate computers and software applications, including enterprise resource planning systems, Google Suite, Microsoft Office, Asana, and Slack.
Strong written, verbal, and interpersonal communication skills to communicate and collaborate across organizational levels.
Ability to influence others positively and handle difficult situations tactfully and confidently.
Consistency and organization in maintaining accurate and timely records.
Ability to work onsite at the Austin-area facility, including daily time on the production floor around hot equipment and chemical handling.

Responsibilities

Direct and optimize compounding operations, including raw material staging, weigh-up, batching, in-process testing, and bulk transfer to filling, to meet schedule, yield, quality, and cost targets.
Run hot-pour, emulsion, and cold-process batching across kettles, mixers, and transfer systems; set and enforce parameters for temperature profiles, mixing speed and time, order of addition, and cooling and hold conditions.
Deliver batches that meet specifications on the first attempt; own batch adjustment, rework, and scrap rates and reduce them.
Ensure every batch record is complete, accurate, and reviewed in real time.
Lead deviation investigations, root cause analysis, and corrective and preventive action in partnership with Quality, and close actions on time.
Keep the compounding area inspection-ready every day under current Good Manufacturing Practices (21 CFR 210/211), ISO 22716, and customer audit standards; represent compounding in FDA, client, and third-party audits and respond to findings with durable corrective actions.
Own compounding standard operating procedures, work instructions, cleaning and sanitization procedures, and equipment logs; keep them current, trained, and followed.
Partner with Research and Development and Process Engineering on scale-up and technology transfer of new formulas; confirm process parameters before the first commercial batch.
Own equipment readiness and utilization for compounding assets; partner with Maintenance on preventive maintenance, calibration, and capital requests.
Build and maintain a documented training and qualification program for every compounding role so that employees only run processes for which they are qualified.
Ensure compounding operations comply with safety standards, including hot surfaces, chemical handling, personal protective equipment, and lockout/tagout, and maintain a safe, organized, and efficient working environment.
Define, track, and report compounding key performance indicators, including schedule attainment, yield, right-first-time performance, deviations, and safety, and use them to prioritize improvement work.
Analyze volume, throughput, and capacity to develop labor, equipment, and shift plans that support business growth.
Manage the department budget, associated costs, and resources.
Participate as a member of the operations team in cross-functional operational decisions.
Collaborate with Planning, Filling and Packaging, Quality, Research and Development, Supply Chain, and Project Management to meet customer commitments.
Select, evaluate, develop, and manage compounding supervisors, leads, and technicians across shifts to ensure efficient operation of the function.
Identify and resolve complex technical, operational, and organizational problems.

Desired Qualifications

Previous experience in contract manufacturing serving multiple brand customers.
Over-the-counter drug manufacturing experience, such as antiperspirant, sunscreen, or similar monograph products.
Experience implementing or operating an electronic batch record or electronic quality management system.
Lean or Six Sigma training with examples of applied improvement work.

Director of Compounding

The Goodkind Co · Round Rock, United States · Full-time · Posted 2026-10-29

Workplace: on_site

Department: Compounding

Description

Overview

Reporting to the Senior Director, Process Engineering, the Director of Compounding is responsible for the oversight of all compounding and batch manufacturing activities in the company. This includes direction, management, and oversight of raw material staging and weigh-up, hot pour (anhydrous) and emulsion batching, in-process control, batch record execution, and release of bulk to filling and packaging. Ensures every batch is made right the first time, on schedule, and in full compliance with cGMP and customer requirements, with the compounding area ready for an unannounced FDA or client audit at all times. Reports operational and quality performance on a regular and timely basis to management. Submits capital purchases and significant proposed actions for approval. Handles special projects as required. The ideal candidate will have deep experience in personal care/cosmetics batch manufacturing with specific hands-on experience in hot pour products such as natural deodorant.

About Us

Founded in 2010 and based in the Austin area, Goodkind is a leading manufacturer of clean and green personal care and beauty products. Goodkind specializes in natural deodorant, skincare, and facial care products. The company has a wealth of experience in the formulation of these products and can develop according to a variety of guidelines from consumer organizations such as Ecocert to EWG, to retailers such as Credo or Sephora.

Goodkind is a certified B Corporation. As such, we balance purpose and profit, considering the impact of decisions across associates, customers, suppliers, community, and the environment. Goodkind believes by following this central multi-stakeholder approach, we are creating optimal value for each stakeholder while leaving the world a better place.

What You'll Do

Direct and optimize all compounding operations, including raw material staging, weigh-up, batching, in-process testing, and bulk transfer to filling, to meet schedule, yield, quality, and cost targets
Run hot pour, emulsion, and cold-process batching across kettles, mixers, and transfer systems; set and enforce process parameters such as temperature profiles, mixing speed and time, order of addition, and cooling and hold conditions
Deliver batches that meet specification on the first attempt; own batch adjustment, rework, and scrap rates and drive them down
Ensure every batch record is complete, accurate, and reviewed in real time, not after the fact
Lead deviation investigations, root cause analysis, and CAPA for compounding events in partnership with Quality, and close actions on time
Keep the compounding area inspection-ready every day under cGMP (21 CFR 210/211), ISO 22716, and customer audit standards; represent compounding in FDA, client, and third-party audits and respond to findings with durable corrective actions
Own compounding SOPs, work instructions, cleaning and sanitization procedures, and equipment logs; keep them current, trained, and followed
Partner with R&D and Process Engineering on scale-up and tech transfer of new formulas; confirm process parameters before the first commercial batch
Own equipment readiness and utilization for compounding assets; partner with Maintenance on preventive maintenance, calibration, and capital requests
Build and maintain a documented training and qualification program for every compounding role so that no one runs a process they are not qualified on
Ensure compounding operations comply with safety standards, including hot surfaces, chemical handling, PPE, and lockout/tagout, and maintain a safe, organized, and efficient working environment
Define, track, and report compounding KPIs (schedule attainment, yield, right-first-time, deviations, safety) and use them to prioritize improvement work
Analyze volume, throughput, and capacity to develop labor, equipment, and shift plans that support business growth
Manage department budget, associated costs, and resources
Participate as a member of the operations team in making cross-functional operational decisions
Collaborate with Planning, Filling and Packaging, Quality, R&D, Supply Chain, and Project Management to keep customer commitments
Select, evaluate, develop, and manage compounding supervisors, leads, and technicians across shifts to ensure the efficient operation of the function
Identify and resolve complex technical, operational, and organizational problems

Requirements

Bachelor's Degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences, or related field, or equivalent experience
Minimum of 10+ years experience in cosmetic, personal care, OTC, or pharmaceutical batch manufacturing
5+ years of management experience leading a compounding or manufacturing function with multiple direct reports
Hands-on experience with hot pour / anhydrous stick products and emulsions at commercial scale, including the process sensitivities of waxes, fatty alcohols, and glycol-based systems
Working knowledge of cGMP (21 CFR 210/211) and ISO 22716; experience hosting or supporting FDA and customer audits
Proven record of improving yield, right-first-time, and schedule attainment in a contract manufacturing or multi-SKU environment
Experience with scale-up and tech transfer from R&D to production
Ability to read and interpret formulas, batch records, COAs, and specifications, and to troubleshoot a batch on the floor
Previous experience in contract manufacturing serving multiple brand customers a plus
OTC drug manufacturing experience (antiperspirant, sunscreen, or similar monograph products) a plus
Experience implementing or operating an electronic batch record or eQMS system a plus
Lean or Six Sigma training with examples of applied improvement work a plus
Experience in fast-paced, high-volume organization, which mandates quick decision making and effective communication
Continuous improvement attitude; ability to suggest and implement best practices
Highly fluent in computer operation with experience with various software applications (ERP, Google Suite, Microsoft Office, Asana, Slack, etc)
Excellent written, verbal, and interpersonal communication skills; ability to communicate and collaborate across all levels of the organization
Demonstrated ability to positively influence others and to deal tactfully and confidently with difficult situations
Highly consistent and organized, with the ability to maintain accurate and timely records
Ability to work onsite at the Austin-area facility, including daily time on the production floor around hot equipment and chemical handling

Benefits

Competitive salary
3 weeks Paid Time Off annually
11 paid holidays annually
Medical, Vision, and Dental 100% paid by the company
401k with company match
Paid parental leave

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About the Company

The Goodkind Co. (Manufacturing)

End-to-end contract manufacturer for personal care

Goodkind Co. provides contract manufacturing and formulation services for personal care brands, handling strategy, custom formulations, manufacturing, and fulfillment. It specializes in anhydrous, water-light products like natural deodorants, serums, and cleansers to boost efficacy and reduce water use and preservatives. It differentiates itself with a focus on anhydrous formulations, strong customer service rooted in founders’ consumer-brand experience, and a sustainability-focused, B-Corporation certified operation with ISO 22716 and cGMP compliance in an 80,000-square-foot facility. Its goal is to be a trusted partner for clean beauty brands, offering reliable, scalable product development and manufacturing from concept to market.

Company size: 51-200
Company stage: Not listed
Total funding: Not listed
Headquarters: Round Rock, TX
Founded: 2019

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