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HANSOH BIO

Hansoh Bio is a U.S.-based subsidiary of Hansoh Pharmaceutical Group Company Limited, a biopharma company founded in 1995. Hansoh Pharma discovers and develops breakthrough therapies for serious diseases and disorders affecting patients around the world, employing 9,000 workers and 1,400 R&D professionals. With over 40 products in commercialization, the Company’s pipeline programs and products cover therapeutic areas such as oncology, central nervous system, anti-infectives, diabetes, as well as gastrointestinal and cardiovascular diseases.

Hansoh Bio is a biotech Research and Development (R&D) arm of Hansoh Pharma based in Rockville, MD, focused on de novo drug discovery and development of novel therapeutics. Hansoh Bio is thrilled to offer exciting opportunities for researchers and scientists to engage in target discovery and pre-clinical candidate development of high impact projects, while being an integral member of a collaborative, passionate, and goal-oriented team.

For more information, please visit Biology and Biophysics – MARYLAND R&D CENTER

We are currently seeking a motivated and multi-talented scientist to join our peptide discovery and development team in Rockville, Maryland. This role will focus on the design, screening, and optimization of peptide-based ligands against biologically relevant targets. The successful candidate will contribute to the development of innovative screening platforms and drive hit-to-lead and lead optimization efforts toward preclinical candidate selection.

This position requires a strong foundation in protein–ligand interactions, peptide chemistry/biology, and a demonstrated ability to integrate experimental and computational approaches.

RESPONSIBILITIES

• Develop novel screening strategies to identify peptide binders

• Drive optimization of peptide hits for affinity, selectivity, stability, and developability

• Leveraging computational tools (e.g., molecular modeling, docking, MD simulations) to inform peptide design

• Apply structure activity relationship principles to guide iterative design cycles

• Interpret structural biology data (e.g., X-ray, cryo-EM, AlphaFold models) to guide optimization strategies

• Work closely with biophysics, structural biology, medicinal chemistry, and in vivo pharmacology teams

• Provide timely communication and presentations

REQUIREMENTS

• Ph.D. degree in biochemistry, biophysics, molecular biology or related areas with 5+ years of research experience. Post-doctoral experience is preferred but not required

• Familiarity with computational chemistry or structural modeling tools

• Strong experience in molecular biology such as RT-PCR, qPCR, etc

• Strong experience in expression, purification, and biophysical characterization of proteins

• Strong understanding of protein–ligand interactions and binding kinetics

• Hands-on experience with biophysical binding assays (SPR, BLI, ITC, etc.)

• Experience with peptide discovery platforms (e.g., phage display, mRNA display, yeast display) is preferred

• Experience in SAR-driven optimization and lead development is preferred

Job Title: Nurse Manager (Endoscopy)

Location : Concord, MA 01742

Shift : 5x8 hour Days 40 hours/week

Contract: 13 +weeks

Start Date: 03/30/2026

Weekly Gross: $4,410

$1,610 is a stipend (nontaxable)

$2,800 is taxable

Local pay ranges: ($95 - $97)/hr.

Strong assistant manager can be accepted with approval**.

NOTE**:- Endoscopy RN's welcome to apply and are accepted at different rate

Experience:

• Minimum of 5 years of nursing experience within specialty area and 3-5 years of supervisory experience preferred.
• An equivalent combination of education and experience which provides proficiency in the areas of responsibility listed above may be substituted for the above education and experience requirements
• Licensure and/or Certification: Current RN license in the state of Massachusetts.

If interested or know someone, reach out directly to my recruiter:

Nitin Gupta (Pacer Staffing LLC)

Email:

Ph. 445-201-1029

Job Description

We are seeking a highly motivated Medicinal Chemistry Team Leader to provide scientific leadership and project management for small molecule drug discovery programs. In this role, you will lead and manage off-site chemistry resources to drive projects from hit identification to preclinical candidate nomination.

Key Responsibilities

• Scientific Leadership: Design targets involving complex multi-step organic syntheses and optimize SAR to improve potency, selectivity, and DMPK profiles.
• Cross-Functional Collaboration: Partner with biology, pharmacology, and computational chemistry teams to integrate data into actionable drug design strategies.
• Project Oversight: Manage timelines and deliverables for assigned programs, including overseeing external synthesis activities and troubleshooting synthetic challenges.
• Communication: Present research findings to senior management and contribute to patent filings and scientific publications.

Required Qualifications

• Education: Ph.D. in Organic Chemistry or Medicinal Chemistry.
• Experience: Minimum of 3+ years of industrial experience in small molecule drug discovery within a biotech or pharmaceutical setting.
• Technical Expertise: Proven track record in lead optimization, structure-based drug design, and modern synthetic methodologies. Experience progressing programs through literature and patent data mining. Familiarity with molecular modeling and visualization tools
• Soft Skills: Excellent interpersonal skills and the ability to thrive in a fast-paced, multidisciplinary environment.

R&D Chemist - Stability Coordinator - Winchester, VA

Winchester, VA - Onsite

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Hubot Tri-Pac, Inc., a contract development and manufacturing company (CDMO) specializing in liquid and aerosol filling for personal care and pharmaceutical marketers, is seeking an experienced R&D Chemist-Stability Coordinator to join our fast-growing team immediately. This position is onsite and located in Winchester, VA.

Job Description

The R&D Chemist -Stability Coordinator and stability coordinator is responsible for coordinating and supporting the site stability program, formulation, and stability sampling activities in compliance with the FDA ICH guidelines, company quality guidelines, SOP’s and other regulatory requirements. This position will be required to work well with the cross-functional teams and will be the key point of contact for all stability programs for OTC, Medical device, and Cosmetic products.

Responsibilities

• This will include initiating stability studies, coordinating stability pulls, making sure the testing schedule of stability samples is met, analyzing stability data, and evaluating trends, and writing stability reports.
• To author stability protocols, interim reports, and reports for stability studies
• This includes routine campaign stability studies and non-routine project stability studies.
• Report the trending of stability data through data management and trend analysis using appropriate software.
• To escalate any trends to the R&D Manager and support any investigations, based on the test data collected.
• To support the business in requests relating to stability data (including temperature excursion assessments, regulatory requests, and investigational work)
• To own and support stability related Deviations, CAPAs and Change Controls, and progress department improvements.
• Manage stability studies following internal procedures, ensuring studies are set up per the protocol.
• The Stability Coordinator will interact with other groups in R&D and other departments (such as QC and production) as required.
• Will collaborate with relevant QC laboratories to ensure stability samples are tested within their specified time frame for actives, and micro.
• Coordinate the shipment of stability samples to outside labs when required.
• Maintain stability tracker for routine annual stability and lab stabilities.
• Good knowledge about lab equipment/test – Viscosity; pH; specific gravity; API’s etc.
• Knowledge of cGMP regulations; GLP.
• Support R&D lab with formulation development for OTC; Cosmetic and Medical device in different forms – Aerosol; liquid and BOV.
• Improve current product formulations.
• Lead formulation development activities with a focus on stability as the primary responsibility.
• Proficient in Microsoft office 365.

Education And/or Experience

• Associate or bachelor’s (B.A or B.S) in a scientific discipline; and 2 or more years related experience and/or training; or equivalent combination of education and experience.
• Must demonstrate knowledge of common analytical tools and techniques.
• Must have previous experience with conducting stability studies and knowledge of statistics.
• Must have previous experience in a GMP environment.

Benefits

Competitive Salary/ Pay & Packages, Vacations, Insurance, 401K, Life Insurance, Disability (Long term/ Short term), and Continuous Training. Work where you are HAPPY! Tri-Pac, Inc. also recognizes the importance of continuing education and offers Education Assistance to our employees to encourage continued personal development and growth.

you for your interest and consideration of a career with Tri-Pac, Inc.

Tri-Pac, Inc. is an Equal Employment Opportunity / Affirmative Action Employer

Please visit our website: RESPONSIBILTIES: 

• Oversee daily laboratory operations, ensuring timely, accurate, and compliant execution of clinical and molecular diagnostic testing.

• Provide leadership and supervision to laboratory staff, including hiring, training, scheduling, performance management, and professional development.

• Develop, implement, and optimize laboratory workflows, processes, and systems to increase efficiency, reduce errors, and support scalability.

• Ensure compliance with all applicable regulatory, accreditation, and safety standards, including CLIA, CAP, OSHA, and internal policies.

• Establish and monitor quality assurance and quality control protocols, ensuring consistent high-quality output and addressing deviations as needed.

• Manage laboratory budgets, inventory, and resource allocation, balancing cost-effectiveness with performance and quality requirements.

• Lead and support cross-functional collaboration with clinical, research, IT, and administrative teams to advance innovation and operational alignment.

• Drive the implementation of new technologies and methodologies, including validation, training, and integration into routine operations.

• Track and report key performance indicators (KPIs) to leadership, using data to inform decisions, identify trends, and guide continuous improvement efforts.

• Foster a culture of accountability, safety, teamwork, and excellence, modeling leadership behaviors that reflect the organization's values and mission.

• Participate in strategic planning and goal setting to support the organization's growth and impact in rare disease diagnostics and beyond.

EDUCATION & DESIRED SKILLS:

• Ph.D. in Life Sciences, Laboratory Science, Molecular Biology, Clinical Laboratory Science, or a related field preferred; a Master’s degree with extensive relevant experience will be considered.

• Certifications, Licensure & Experience: ASCP Medical Technologist (MT/MLS) or equivalent certification preferred.

• Minimum of 10 years of progressive clinical laboratory experience, including at least 5 years in a leadership or management role overseeing multidisciplinary laboratory environments. Relevant experience will be considered.

• Demonstrated experience directing operations across multiple high-complexity clinical laboratory disciplines, including but not limited to clinical chemistry, immunology, molecular genetics, and other molecular diagnostic testing areas, with responsibility for assay implementation, validation, and operational oversight.

• Extensive experience in clinical laboratory operations, quality management, and regulatory compliance, including CLIA high-complexity testing requirements, CAP accreditation standards, and OSHA laboratory safety regulations.

• Demonstrated expertise in laboratory workflow design, process optimization, and integration of advanced diagnostic technologies, including automated chemistry platforms, immunoassay systems, and molecular diagnostic platforms such as PCR, NGS, or other nucleic acid–based testing systems.

• Proven ability to manage multidisciplinary laboratory teams and cross-functional operations, ensuring coordination between scientific, technical, and operational groups to support scalable laboratory services and clinical testing delivery.

• Excellent organizational and time management skills, with the ability to prioritize multiple responsibilities and maintain attention to detail in a complex laboratory environment.

• Exceptional critical thinking, judgment, and problem-solving abilities; able to respond with urgency and accountability in high-stakes clinical and operational situations.

• Strong interpersonal and communication skills, with the ability to build relationships and communicate effectively across all levels, both internally and externally, including physicians, researchers, regulatory bodies, and external partners.

• Collaborative and team-oriented mindset, with a commitment to fostering a positive workplace culture and championing organizational values.

• Proficiency with laboratory information systems (LIS), quality management systems (QMS), and laboratory data platforms, along with standard productivity tools (e.g., Microsoft Office Suite).

Job Type: Full-time

Benefits:

• 401(k)

• 401(k) matching

• Dental insurance

• Health insurance

• Life insurance

• Paid time off

• Vision insurance

Schedule:

• Monday to Friday, on-site 

Position Title: Early Research & Development Scientist

Work Location: Tucson, AZ, 85755

Assignment Duration: 12 Months

Work Arrangement: Onsite

Key Responsibilities:

• Initiate, direct, and execute scientific research, product early development, and manufacturing process strategies to support new and existing products.

• Investigate the feasibility of applying scientific principles and concepts to potential inventions and problems in the pathology lab assay space.

• Plan and execute laboratory research utilizing thorough technical and theoretical understanding of numerous techniques.

• Developing new formulations for staining, data analysis, creative applications of AI tools as part of the Research Staining Technology Team.

• Analyze data, evaluate results, form conclusions, and implement process or document improvements.

• Prepare technical reports, summaries, protocols, and quantitative analyses.

• Present and discuss experiment results within the department and project team.

• Participate in the development of patent applications and efforts to define new components, products, or processes.

• Serve as an in-house and outside consultant, potentially advising top management or acting as a corporate scientific affairs spokesperson.

• Ensure complete and accurate laboratory documentation and electronic files, and adhere to company policies for GMP, GLP, and Design Control.

Qualification & Experience:

• Entry-level Ph.D.

• Master’s degree with 3+ years of experience

• Participate in cell culture experiments and maintain live cell cultures.

• Apply advanced scientific knowledge to projects and utilize Design of Experiments (DOE) where appropriate.

• Previous experience in tissue diagnostics, including immunohistochemistry in a pathology lab environment.

• Knowledge of or experience in primary stains and special stains.

• Experience with Electronic Lab Notebook (ELN).

• Familiarity with SAFe Agile methodologies.

• Image analysis programming experience/scanning of images.

• Experience with Digital Pathology.

• Tissue culture, specifically spheroid and organoid models.

JOB ID:PHS-6210

Position: Angio/Interventional Rad Tech

Shift Schedule: 07:00 - 15:30

Location: Inglewood, CA, 90301

Start date: 03/30/2026 - 06/28/2026

Pay: $80-$85 per hour

Job Summary:

Intervention Radiology Technologist that can assist performing Angiography Examinations. Please apply candidates with experience in assisting performing Line Placements, Angiograms, Kyphoplasty, Percutaneous Nephrostomy Exam, ETC. & familiar with GE Innova equipment. Interventional Radiology Tech/Angiography Tech. RT(ARRT) required. 7am-3:30 plus call/ Ideally 5 days per week, 8 hr shifts however as needed/ M-F IR Technologist Traveler

The Angio/Interventional Radiologic Technologist assists in performing minimally invasive, image-guided vascular and non-vascular procedures under the supervision of an interventional radiologist or other qualified physician. This role involves operating fluoroscopic and angiographic imaging equipment, preparing patients, ensuring radiation safety, and maintaining sterile technique throughout procedures.

Key Responsibilities:1. Procedure Support & Imaging:

• Assist physicians in performing interventional radiology procedures, including angiography, stent placements, embolization, biopsies, and drainage procedures.
• Operate and maintain specialized imaging equipment such as fluoroscopy and digital subtraction angiography (DSA) systems.
• Ensure high-quality imaging while minimizing radiation exposure to patients and staff.

2. Patient Care & Safety:

• Prepare patients for procedures by explaining the process, obtaining consent, and positioning them appropriately.
• Monitor patient vital signs and respond to any emergencies during procedures.
• Maintain a sterile field and adhere to infection control protocols.

3. Equipment & Inventory Management:

• Prepare and set up sterile trays, guidewires, catheters, contrast media, and other necessary equipment.
• Perform routine maintenance and quality checks on radiologic equipment.
• Ensure appropriate inventory levels of interventional supplies.

4. Documentation & Compliance:

• Accurately document patient history, procedural details, and post-procedure observations in the electronic health record (EHR).
• Adhere to hospital policies, radiation safety standards, and HIPAA regulations.

Qualifications: Education & Certification:

• Associate’s or Bachelor’s degree in Radiologic Technology or a related field.
• Current ARRT (American Registry of Radiologic Technologists) certification in Radiography (R) required.
• ARRT certification in Vascular-Interventional Radiography (VI) preferred or must be obtained within [specific timeframe].
• State licensure (if required).
• BLS (Basic Life Support) certification required; ACLS preferred.

Experience:

• 2+ years of experience in diagnostic radiology; prior interventional radiology or angiography experience preferred.
• Strong understanding of human anatomy, pathology, and interventional techniques.

Precision Scans is an equal-opportunity employer, committed to cultural

diversity. Precision Scans will provide equal consideration for employment to all

qualified applicants without regard to their race, religion, ancestry, national

origin, sex, sexual orientation, age, disability, marital status, domestic partner

status, or medical condition.

Position Overview

A hospital-based clinical laboratory in Central PA is seeking a Microbiology Laboratory Director to provide scientific, operational, and regulatory leadership for a high-complexity microbiology laboratory. This role is responsible for overseeing laboratory operations, ensuring compliance with regulatory standards, guiding test development and validation, and supporting clinical teams with microbiology expertise.

The ideal candidate will bring strong leadership skills, a commitment to quality and regulatory compliance, and experience managing microbiology testing in a clinical laboratory environment.

Key Responsibilities

Laboratory Leadership & Oversight

• Provide medical and scientific direction for all microbiology laboratory operations
• Oversee daily laboratory activities to ensure quality, accuracy, and efficiency
• Support and mentor laboratory supervisors, technologists, and technical staff
• Collaborate with hospital leadership and clinical teams on laboratory strategy and patient care initiatives

Regulatory Compliance & Quality

• Ensure laboratory compliance with CLIA, CAP, and applicable regulatory requirements
• Maintain and oversee quality management programs, including proficiency testing and quality assurance initiatives
• Review and approve validation and verification studies for new assays and instrumentation
• Participate in regulatory inspections and implement corrective actions when necessary

Test Development & Technical Expertise

• Provide guidance for microbiology test development, validation, and implementation
• Evaluate new technologies, platforms, and workflows to enhance laboratory services
• Review and approve standard operating procedures and technical documentation

Clinical & Operational Collaboration

• Serve as a subject matter expert for microbiology testing and infectious disease diagnostics
• Partner with infectious disease physicians, pharmacy, and infection prevention teams
• Support antimicrobial stewardship initiatives and clinical decision-making

Qualifications

Education

• Ph.D. in Microbiology, Clinical Microbiology, or a related field

Experience

• 2–5 years of clinical microbiology laboratory experience in a high-complexity setting
• Experience in hospital or health system laboratories preferred
• Prior leadership or supervisory experience is highly desirable

Certifications (Preferred)

• ABMM (American Board of Medical Microbiology) or eligibility preferred

Skills & Competencies

• Strong knowledge of clinical microbiology methodologies and instrumentation
• Familiarity with regulatory standards including CLIA and CAP
• Excellent leadership, communication, and organizational skills
• Ability to collaborate effectively with clinical and administrative stakeholders

Compensation & Benefits

• Salary Range: $180,000 – $230,000 annually
• Comprehensive benefits package including:
• Medical, dental, and vision insurance
• Retirement plan with employer contribution
• Paid time off and holidays
• Continuing education support
• Relocation assistance may be available

About us:

At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 21 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories.

It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Lighthouse Lab Services is committed to working and providing reasonable accommodation to individuals of all abilities, including persons with disabilities.

If at any time during the application process, you need an accommodation, please contact for assistance.

Lighthouse Lab Services | 844-974-1929 | LLS3

We are seeking a dynamic and detail-oriented Analytical Chemist to join our innovative laboratory team. In this role, you will be at the forefront of quality assurance and product development, utilizing advanced analytical techniques to ensure our products meet the highest standards of safety, efficacy, and regulatory compliance. Your expertise will drive critical testing processes, support regulatory submissions, and contribute to continuous improvement initiatives. This position offers an exciting opportunity to apply your scientific skills in a fast-paced environment committed to excellence and innovation.

Responsibilities:

• Conduct comprehensive chemical analyses using techniques such as spectroscopy, chromatography (gas chromatography and high-performance liquid chromatography), and microscopy to characterize raw materials, intermediates, and finished products.
• Perform wet chemistry procedures, including titrations, pH measurements, and sample preparations in accordance with Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs).
• Calibrate laboratory instruments such as spectrophotometers and chromatographs regularly to ensure accurate and reliable results.
• Maintain detailed documentation of all experiments, test results, calibration records, and quality control data within Laboratory Information Management Systems (LIMS).
• Ensure compliance with FDA regulations, CGMP (Current Good Manufacturing Practices), and other regulatory standards during all testing activities.
• Support quality control initiatives by verifying product specifications, conducting stability studies, and troubleshooting analytical issues.
• Collaborate with cross-functional teams, including biochemistry, microbiology, and quality assurance, to optimize analytical methods and improve laboratory workflows.

Experience:

• Proven laboratory experience in analytical chemistry or related fields within a regulated environment, such as pharmaceutical or biotechnology industries.
• Hands-on expertise with spectroscopy techniques, including UV-Vis, IR, or atomic absorption spectroscopy.
• Strong knowledge of chromatography methods—gas chromatography (GC) and high-performance liquid chromatography (HPLC)—and their application in quality testing.
• Familiarity with wet chemistry techniques and microbiological testing procedures is highly desirable.
• Experience working under GLP guidelines and understanding FDA regulations relevant to pharmaceutical or biotech manufacturing.
• Proficiency with laboratory information management systems (LIMS) for data entry, analysis, and reporting.
• Background in biochemistry or microbiology is advantageous for supporting diverse analytical projects.

Join us to be part of a passionate team dedicated to advancing scientific excellence!