Location: Sumter, SC
Unparalleled schedule flexibility and supportive company culture Dynamic company partnerships to ensure career stability Meaningful work-life balance with flexible schedules Highly competitive rates + 401K Plan with company match Healthcare benefits package Online CEU Credits Promotion / Advancement / Transfer Opportunities Referral bonus program eligibility Employee Assistance Program Excellent management and support team Student mentor program We offer additional benefits and perks, please reach out today About Us: Tender Touch Rehab is part of Enhance Therapies , a family of therapy companies with more than 30 years of industry leading experience.
With over 7,000 therapists in 28 states
and growing, we provide quality rehabilitation services to homecare, sub-acute, long-term care, outpatient, hospital, and assisted living facilities throughout the nation.
Why become a Physical Therapist with Tender Touch Rehab? Company Culture - Become part of a close-knit team of passionate clinicians who strive to professionally develop and grow together through collaboration. Compensation Package - Competitive rates, full benefits package, 401k plan, continuing education allowance and much more. Clinical Advancement - Additional training, mentorship, and direct support to help develop your career. Opportunities - Focus on the setting YOU are passionate about! Upward Mobility/Leadership
Oversight - A focus on promoting success through therapists invested in leadership roles and internal promotions.
Quality Care Starts with US - We demonstrate empathy and compassion to all team members and patients whom we treat. Ways to Get Involved - Clinical mentorship and community outreach opportunities. Qualifications: Physical Therapist provides a comprehensive physical therapy evaluation based on MD’s orders. Physical Therapist provides comprehensive treatment plans including long and short-term goals, frequency, duration, and treatment modalities. PT ensures MD orders are obtained for evaluations, treatments, re-certifications, and discharges.
PT Provides comprehensive treatment to patients utilizing modalities and modify patient treatment as indicated while adhering to precautions. Physical Therapist completes all required documentation Requirements: Graduate of an accredited university with a B. S. Doctorate, MA, or MS in Physical Therapy that the APTA recognizes PT holds a current license and/or registration as a Physical Therapist in-state (as applicable)#TT1 Pay Range: USD $39.00 - USD $55.00 /Hr. For more details: jobs-search. org/physical-therapist_sumter-c446314/job_i1965995493
Analytical Chemistry (AC) Management. Performs Quality Control testing and data review to support timely release of product in weekly basis. Effective development, optimization, and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products, and stability studies.
Proficient in Empower Software and other laboratory software use in QC environment for chromatographic, spectroscopic methods as well as wet chemistry. backss testing methodologies and their application to different sample matrix, instrumentation and will include evaluation of testing results from contract laboratories to be sure that the agreed methods and
testing parameters were properly followed. Maintains current knowledge of latest technological and scientific trends and serves as an analytical science resource for the rest of the group.
Mentor and train chemists in the proper execution, including interpretation of validation studies. Responsible for producing hazardous waste from it point of generation. Managing all produced in accordance with RCRA and SCDHEC regulations to include: proper containers, accumulation, labeling, marking, and storage. Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives. Communicate effectively with other
departments within the organization and function within a team environment.
Regular attendance is required. Minimum Requirements: Able to develop analytical methods for chromatographic, spectroscopic, titrimetric, and wet chemistry analyses. Must be proficient on laboratory instrument trouble shooting. In-depth knowledge of strategies of analytical method development and specification setting for raw materials and finished products. Knowledge i n most of laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS, GC-MS, ICP-MS, HPTLC and test methods. Knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods, and Mass spectrometry.
Proficient in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner. Experience in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation, and mechanical manipulation. Knowledge of statistical techniques, such as data trend analysis and design of experiments, is highly desirable. Proficiency in reviewing and interpretation of laboratory data.
Detailed knowledge of principles of routine laboratory operations. Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to medical and/or nutritional supplement GLP/GMP is strongly desired. Demonstrated aptitude to function in a dynamic fast-paced environment. Education and Experience A Bachelor's degree with 10 years of experience in validation and development of analytical methods for nutraceuticals and/or medical samples in a GMP environment. A Master's degree and a minimum of 5 years of technical experience is preferred.
Extensive experience may be accepted in lieu of an advanced degree. A degree in analytical chemistry, biochemistry, chemical engineering, or related fields is strongly preferred. A need to work on the bench to accomplish tasks along with the Analytical Chemistry team. Supervisory Responsibilities: None Job Posted by Applicant Pro
activities either individually or as part of a team that may include the collection of field data, completing field tests, observation of construction activities, implementing health and safety procedures, oversight of related subcontractor services and other field related activities; Field duties may include drilling oversight, well installation, analytical sampling, gauging and surveying activities, operation and maintenance of remediation systems; Assisting in the field sampling and testing of various environmental media; Compiling and completing field data for multiple sites; Client interaction and communication; Candidate must have ability to work independently with minimal supervision;
Coordination with task and project managers, working with on-site subcontractors and field staff; Calibrating and maintaining field instrumentation, QA/QC data sheets and field logs in support of environmental investigations; Performing field activities related to environmental compliance, stormwater pollution prevention and erosion and sediment control inspections and reporting; Assisting with the development and distribution of field notes, meeting minutes, project action item lists, internal tracking of projects activities and general project coordination activities in support of project managers; Assisting in the field interpretation of project design drawings and technical specifications
and communicating findings with the project engineers and geologists; Position Requirements and Qualifications: Bachelor's Degree in Geology, Environmental Science or other science related field.
Will also consider commensurate combination of education and experience. Must be able to work in both indoor and outdoor environments Valid Driver's License and ability to authorize our review of a motor vehicle driving record for the past 5 years; Ability to work using hand tools and testing equipment; Required to lift objects of up to 50 lbs Consistent travel for field work required locally and throughout the Southeastern United States Good written and verbal communication skills; Basic knowledge in the operation of smart phones and computers for communication and recording time worked Must pass a pre-employment background and drug test Job Posted by Applicant Pro
new services, we never forget the values that made us who we are as a company. We are a team. A family. A group of smart, talented, big-hearted individuals working together for the success of our customers and the growth of our communities. AND WE HONOR OUR COMMITMENTS What we do at Ortec is complicated at times.
Why we do what we do is not complicated: We want to make a difference for our customers and our communities around us. How we do what we do is also not complicated: everything starts with Integrity. WHY ORTEC? The foundation of Ortec is our talented, dedicated employees. Our commitment to delivering chemical manufacturing services with measurable quality has made us a trusted
partner to some of the most familiar names in business. Our success is drawn from the experience, energy and teamwork of our employees, who consistently deliver results by anticipating change and executing solutions with confidence and passion.
At Ortec, you'll be working with the latest technologies and tools, not to mention some of the industry's best and brightest minds. From the top down, this type of commitment and energy is radiated throughout the company. The result is a growing, dynamic, and rewarding place to work a company where we work as many and we win as one. You are a name, not a number! We offer an excellent benefit package, including: Competitive benefits with onsite
medical care for free401k with match Medical, Dental, and Vision and much more!
POSITION SUMMARY Serve as a focal point for providing technical support and expertise to manufacturing and plant operations. Provide hands-on support to production, sales, lab, and customers on technical issues for current and future technology. ESSENTIAL FUNCTIONS Provide in-depth, thorough knowledge of Production processes, equipment, and operations. Communicate and interact with customers or potential customers, regarding processes, technology, production logistics, quality, and safety. Investigate the root cause of customer complaints and recommend corrective actions. Observe, critique and optimize chemical processes in safety, efficiency, quality, performance, technical aspects.
Lead in the scale up of new products from lab to plant trials. Develop, improve, and customize products, equipment, formulas, processes, and analytical methods in support of customers. Participate and lead in technical meetings relating to manufacturing operations, product quality, and production efficiency. Coordinate technology transfer to and from customers. Provide work direction, technical training, and guidance to operations. Direct, coordinate, and advise personnel in test procedures for analyzing components and physical properties of materials relating to new technology or customer methods.
Monitor process and quality data for trends and cause/effect analysis.
will assist to ensure methods are accurate, precise, and robust for use of testing release samples. The QCCII must have a strong understanding of experimental design, chemical theory and analytical instrumentation such as HPLC, GC, ICP-MS/ICP-OES. The QCCII must be knowledgeable in all QC routine functions and capable of being relied upon to perform any and all QC related functions.
The QCCII is expected to be capable of independently executing in-house methods and procedures and performing them as written with little to no assistance based on their extensive experience. Perform release, stability and special request testing of finished products and raw materials following Standard Operating
Procedures (SOPs), in-house test methods, and/or compendial methods. Be able to make decisions based on facts, experience and intelligent backssment. Independently manage projects assigned by management within expected/established time frames.
Stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the QC Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation practices. Assist laboratory personnel in resolving Out of Specification (OOS) results in accordance with laboratory investigation procedures if assigned. Assist in training of new laboratory personnel and document training in accordance
with established laboratory SOPs and the Nutramax training program.
Follow current Good Manufacturing Practice (c GMP) documentation guidelines to record all procedures in a timely fashion. Maintain a safe work environment and will ensure that all equipment used in the testing procedures is calibrated and properly maintained. Perform other assigned duties as may be required in meeting company objectives. Communicate effectively with other departments within the organization and function within a team environment. Regular attendance is required. Minimum Requirements: Five or more years of laboratory experience in a c GMP facility, including experience with operation of laboratory instrumentation including Gas Chromatography (GC) and/or Liquid Chromatography (LC) required, troubleshooting, project management, generation and revision of SOPs and test methods.
Method optimization, validation and/or development experience is a requirement for this position. Effective interpersonal, self-motivation, communication skills and the ability to interact with all levels of personnel are required. Education and Experience: A Bachelor of Science (B. S. ) or Bachelor of Arts (B. A. ) degree in a science-related field such as Chemistry, Biochemistry or Biology preferred. Supervisory Responsibilities: N one Job Posted by Applicant Pro
