Formulation Chemist Salary at Particle Sciences BETA

Job Description Job Description Department: Quality Assurance Job Title: Technical Writer FLSA Status: Exempt 1. Role Purpose: Primary responsibility is the preparation of technical documents, including Standard Operating Procedures, Manufacturing Batch Records, Protocols, and Reports. Additional responsibilities may include investigating and documenting all deviations and customer related complaints related to the Manufacturing, Packaging and Shipping/Receiving departments by reviewing all related documents, and interviewing relevant personnel so as to identify the root cause and corrective actions required. Also, to change or correct any related documents pertinent to the conclusion of the investigation (i.e., SOP’s) while maintaining compliance with cGMP requirements, FDA, OSHA, EPA, and DEA. 2. Key Duties & Responsibilities: Prepare and review Master production and packaging batch records Prepare and review Validation Protocols and reports Prepare Quality Event Records (including d

Job Description Job Description Department: Quality Assurance Job Title: Technical Writer FLSA Status: Exempt 1. Role Purpose: Primary responsibility is the preparation of technical documents, including Standard Operating Procedures, Manufacturing Batch Records, Protocols, and Reports. Additional responsibilities may include investigating and documenting all deviations and customer related complaints related to the Manufacturing, Packaging and Shipping/Receiving departments by reviewing all related documents, and interviewing relevant personnel so as to identify the root cause and corrective actions required. Also, to change or correct any related documents pertinent to the conclusion of the investigation (i.e., SOP’s) while maintaining compliance with cGMP requirements, FDA, OSHA, EPA, and DEA. 2. Key Duties & Responsibilities: Prepare and review Master production and packaging batch records Prepare and review Validation Protocols and reports Prepare Quality Event Records (including d

Job Description Job Description Department Technical Services Job Title Technical Services Supervisor FLSA Status Exempt Role N/A Sub Role (If any) N/A Reports To Director of Operations 1. Role Purpose: The Supervisor of Technical Services is responsible for department activities in providing technical and proposal writing for the organization. This includes writing Standard Operating Procedures, Technical Transfer Documents, Validation Reports, Manufacturing Batch Records, Protocols, Pre-Development and Pharmaceutical Development Reports, investigations and other various documents. Additionally, the position will assist with the development and delivery of process records for production. Technical Services role requires preparation of process validation protocols, process validation reports, and commercial batch records preparation. Manages documentation compliance and change control for R&D. Execute all functions in accordance with current FDA regulations, ICH guide lines, USP method

Industrial Formulation Chemist/Product Development/Lab Manager DESCRIPTION Ardex Labs is an industry-leading manufacturer of automotive detailing products, established in 1949. We are a family-owned and operated organization. Ardex formulates and produces an extensive array of professional automotive detailing products in our Philadelphia-based plant. Drawing on decades of experience, we supply everything from the from economical and volume oriented products, to the high end boutique detail world. Ardex Labs strives for constant innovation and improvement of current products and processes. RESEARCH & DEVELOPMENT Ardex Labs employs an in‐house, full-time, industrial formulation chemist who, working in conjunction with our extensive salesforce and customers, creates products that fulfill all of the industry’s needs in an ever-changing environment. Our company is driven by our passion for success and founded on strong teamwork and family values. JOB RESPONSIBILITIES The Formulation Chemis

SUMMARY The Research Fellow, Formulation Development Scientist provides scientific leadership for, and actively contributes to, the early- and late-stage formulation and process development of oral drug products. This position also contributes to drug product development and life cycle management by designing and developing formulations and processes for preclinical & clinical evaluations as well as for commercial technology transfer. This position works cross-functionally with internal departments and external partners on formulation and process development related activities and issues. The Research Fellow, Formulation Development supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. RESPONSIBILITIES Independently designs studies and conducts risk assessments as per target product profiles to build in quality-by-design (QbD) during formulation and process development. Independently develops robust formulations and manu

Who we are: The Secant Group is an advanced technology biomaterials company headquartered in Telford, Pennsylvania, with manufacturing facilities in Quakertown and Perkasie, Pennsylvania. Secant provides innovative solutions through next-generation materials, structures, textile designs, and process technologies for the medical device, pharmaceutical, aerospace and energy markets. What we are looking for: Based in our Telford, PA facility, the Staff Scientist is responsible for driving innovation and development of polymeric biomaterials in the controlled release field. The Staff Scientist will primarily work in a laboratory-based role innovating and formulating polymer drug products for our controlled release platform. The Staff Scientist is responsible for designing and conducting experiments to create next-generation drug-loaded polymer products for the Translational Product Development team. The Staff Scientist will have daily exposure to chemical lab environment, and exposure to m

Job Description Job Description Job Title: Associate Product Development Scientist Location: Penn Life Sciences, Langhorne, PA Department: Research & Development Job Summary: Penn Life Sciences is seeking an experienced Associate Product Development Scientist to lead the formulation and process development of sterile pharmaceutical products (including injectables). This role requires a deep understanding of sterile product development, aseptic processing, and regulatory compliance to drive innovation and commercialization efforts. The ideal candidate will have significant experience in formulation science, process optimization, and regulatory strategy, with the ability to lead cross-functional teams and support regulatory submissions. Key Responsibilities: Formulation & Process Development: Design, optimize, and implement robust pharmaceutical formulations for sterile injectable products to ensure stability, bioavailability, and manufacturability. Analytical Testing & Evaluation: Overs

Accupac seeks to hire a Research and Development Formulation Manager to join our team in Mainland, PA! Position Summary: As Manager, R&D Formulation, you will lead the day-to-day operations of the formulation lab and manage a team of chemists and technicians responsible for developing personal care products (e.g., skincare, haircare, oral care, etc). You will oversee project execution across categories, manage lab operations, and ensure formulation readiness from initial brief to customer delivery. You’ll serve as the key link between lab execution and strategic innovation by supporting customer projects, managing testing documentation, and driving lab-based initiatives including safety and sustainability. Key Responsibilities (Updated & Integrated): Team & Lab Leadership Direct lab activities and supervise a team of chemists and technicians across multiple personal care categories. Lead onboarding and formulation briefing of new project wins across skin, hair, and oral care. Manage st