Formulator Salary at Tatua BETA

Formulation Scientist - Sun Care QUALIFICATIONS: Minimum education required for competent performance: BS Degree in applicable field 2+ years of experience in measurement sciences & test method development Instrumentation experience with SPF In vitro testing background Minimum experience (number of month/years and type of work experience beyond formal education) required for competent performance: 2-4 years of experience preferred, 1-2 years of sun care formulation testing preferred eg. Labsphere Lab experience and measurement science is a must-have Experience in Analytical AOX assays preferred Able to test formulations to screen new technologies Process and analyze data from the measurements Able to execute experiments independently Manage laboratory samples Execute physical testing of samples, competitive analysis Ability to handle and prioritize multiple tasks/deliverables Adhere to safety procedures of laboratory Working knowledge of standard instrumentation (pH meter, viscometer,

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

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

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

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

Insight Global is looking for a Formulation Scientist to join the team Research and Development organization of a large consumer healthcare company. This individual will be responsible for batching, stability testing, and compliance documentation within electronic systems. They will be supporting an ongoing compliance initiative and will be focusing on laboratory activities including formulation and testing. The ideal candidate will have industry experience within the personal care or cosmetics industry in a laboratory environment. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin,

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