Research Associate Salary at Act Research BETA

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packagin

**DESCRIPTION** Ensure Quality Control: Youll monitor production processes to ensure products meet Cummins high-quality standards. Optimize Efficiency: By identifying and implementing process improvements, youll help increase manufacturing efficiency. Support Safety Initiatives: Youll actively participate in safety programs and ensure compliance with safety regulations. Collaborate with Teams: Working closely with other departments, youll help streamline operations and solve production issues. Maintain Equipment: Regular maintenance and troubleshooting of manufacturing equipment will be part of your role to minimize downtime. Document Processes: Youll keep accurate records of production activities, contributing to better tracking and analysis. Train New Employees: Sharing your knowledge and skills, youll help train new team members to ensure they are well-prepared. Drive Continuous Improvement: Youll be involved in continuous improvement initiatives, aiming to enhance overall productio

Starting at $11 per hour!!! The Retail Associate assists the store management team in reaching the operational goals of the site by functioning in various capacities within the retail location. The titles of the various jobs the Retail Associate may be called upon to learn and work include: Cashier, Textiles or Wares Producer, Donation Door Attendant, eCommerce Producer, e-Books Producer, and Rack or Cart Runner. Example Duties and Activities Cashier: Rings up customer orders, maintains a balanced drawer, and follows all cash handling procedures and protocols. Provides general information about Goodwill programs to educate customers and answer questions. Directs all higher-level questions to the appropriate associate or manager. Maintains cleanliness of the sales floor (purge, size, run racks, and merchandise). Textiles or Wares Producer: Sorts product to identify quality and value (checks for holes, missing buttons, defective zippers, or stains and cleans as needed) and properly barbs

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packagin

Vaccine Clinical Research Associate 3 to 5 protocols 5 to 8 sites 8 to 10 days on-site per month Therapeutic areas: Vaccines trials. Vaccine trials are fast-paced with quick database cleaning demands. Requirements: Must have a four-year degree, completed all visits independently and have two years of independent monitoring. Open to any therapeutic experience. What will you be doing? As a Clinical Research Associate, you will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. Applies knowledge of ICONs policies and procedures Demonstrates excellent written and oral communication Demonstrates excellent knowledge of ICH/GCP Displays ability to manage investigative sites to facilitate trial deliverables Demonstrates ability to escalate issues appropriately Conducts monitoring to

Your Role at Client s part of the sustaining engineering team, you will be responsible for design changes for medical device products such as hospital beds and equipment. The engineering design changes may be related to design improvements, new compliance requirements, or supply chain support. What you'll be doing s a packaging engineer on the team, you will be responsible for performing design analysis and engineering releases for small to medium projects or participate in portions of larger complex projects. The projects will primarily involve product and accessory packaging design and development but may also include labeling, documentation, or other more general product updates. Perform root cause analysis to investigate product damaged during shipping and develop corrective actions. Develop verification and validation plan for new packaging design pply new technical tools and concepts as needed with support from other team members. Implement design changes for product and accessor

JOB DESCRIPTION: The Team Leader oversees, monitors, and coordinates production team activities, giving importance to individual members and overall team's achievement of established goals. Ensures teams goal is aligned with and representative of the overall company's directive. Acts as a liaison between team members and the rest of the organization. Must be familiar with standard concepts, practices, and procedures within a particular field. Relies on limited experience and judgment to plan and accomplish goals. Performs a variety of tasks. Typically reports to a manager or supervisor and assumes supervisory duties in their absence. A certain degree of creativity and latitude is required. ESSENTIAL DUTIES AND RESPONSIBILITIES: Maintain time and production records Responsible for the JD Edwards system Read standards Run lines as needed Assist with investigating quality issues (5-Why) Check under machine for things that should not be there (parts or components) Check all emergency stop

JOB DESCRIPTION: Fully responsible for accurately translate all official documents like operational work instructions, visual aids, medical forms, HR presentations, etc. into Spanish. The candidate also will need to do live translations during meetings, trainings or emergency medical situations. ESSENTIAL DUTIES AND RESPONSIBILITIES: Ensure translated content conveys original meaning and tone Cross-reference specialized dictionaries and translation tools to check quality of translation Proofread translated texts for grammar, spelling and punctuation accuracy Follow up with production team members to ensure translation meets their needs and that they are clear and understandable Edit content with an eye toward maintaining its original format (e.g. font, format, structure, etc.) REQUIRED KNOWLEDGE, SKILLS, EDUCATION, AND ABILITIES: Proven work experience as a Translator, Interpreter or similar role Fully Bilingual English/Spanish (read, write and speak) Excellent Attitude, attendance and