location_0_addressRegionName

location_0_addressCountryName

ONSITE

PERMANENT

FULL_TIME

jobPosting hiringOrganization as json hashed.

ADAPTED_NOW

UNKNOWN

YEAR

Biotech and Pharmaceutical

SAP, LIMS, DeltaV, MQTT, UNS, Aveva PI, Data Lakes, Process Monitoring systems such as JMP, Tableau, Python, JSON, YAML, SQL, or Git, Github, C#, SQL, XML, REST, OPCUA, Data Modeling, Web Development, Responsibility will be to craft and develop robust IT architecture solutions tailored to sophisticated business challenges within the pharmaceutical manufacturing domain.

KBSkills

ACTIVE

Pacific Technical Resources, LLC.IT/Engineering Recruitment Professionals"Helping to build Great Companies and Great Lives"  Serious direct hire career opportunity for a Pharmaceutical MESSolutions Architect Engineer with Enterprise Implementation Experience for a Global Pharmaceutical Leader in Lebanon Indiana Relocation assistance is available.  Employer is serious and urgent to hire.  Underway is construction a new campus to manufacture Clinical Trial (CT) Active Pharmaceutical Ingredient (API). Responsibility  will be to craft and develop robust IT architecture solutions tailored to sophisticated business challenges within the pharmaceutical manufacturing domain. Lead the implementation of complex MES, driving the transition to paperless execution from the facility's inception.  Basic Qualifications: Bachelor’s degree in software engineering, Computer Science, Computer Engineering, or a related field.3+ years of experience working with Pharmaceutical Manufacturing Execution Systems (e.g. Data solutions, MES technologies such as Rockwell Automation Pharma Suite, Emerson Syncade, Siemens Camstar, or Werum PAS-X). 3+years of experience on Active Pharmaceutical Ingredients(API) manufacturing facilities. Additional Information:  Skills and CertificationsLeading Implementation of Pharma MES SystemsPharma Manufacturing Execution Systems (3+ years experience)API manufacturing facilities (3+ years experience)Data solutions, MES technologies such as Rockwell Automation Pharma Suite, Emerson Syncade, SiemensExperience leading or supporting the Computer System Validation of IT platforms including Data IntegrationSAP, LIMS, DeltaV, MQTT, UNS, Aveva PI, Data Lakes, Process Monitoring systems such as JMP, Tableau,Python, JSON, YAML, SQL, or Git, Github, C#, SQL, XML, REST, OPCUA, Data Modeling, Web Development,  If you are qualified and open to working in Lebanon Indiana  and seeking a new career opportunity please send your resume to Clara at cfoo@pacifictechnicalresources.com  Pacific Technical Resources, LLC. specializes in IT/Engineering Recruitment Placement with roots from Honolulu, Hawaii is headquartered in Phoenix, Arizona.  We bring extensive experience with IT/Engineering recruitment along with a holistic philosophy of valuing people. We have special industry expertise with Energy Solutions and Aerospace/Defense. Please visit us on our website at www.pacifictechnicalresources.com

Pacific Technical Resources LLC

Pharmaceutical MES Architect (Relo Indiana)

Active Pharmaceutical Ingredient (API)

Aerospace and Defense

Clinical Trial

Computer Engineering

Computer Science

Computer Systems

Construction

DeltaV

Drug Manufacturing

Enterprise Architecture

Information Architecture

Information Technology & Information Systems

Laboratory Information Management System (LIMS)

Leadership

Manufacturing

Manufacturing Execution Systems (MES)

Philosophy

Rockwell Automation

Software Engineering

System Validation

Tableau

Technical Recruiting

monster

OFFSITE

Unclassified Occupations

Co-Op positions are full time, 40 hours per week that last close to 6 months, and we hire 4-6 Co-Ops each cycle: Positions posted in February for a July – December Co-Op. These are amazing opportunities for students to learn and make potentially significant contributions to a vibrant biotech company.

Visterra hires talented students into Co-Ops and Internships throughout the calendar year across multiple departments, including Research, Clinical Development, Pharmaceutical Sciences & Technology and other corporate functions like Finance or Human Resources.  These are amazing opportunities for students to learn and make potentially significant contributions to a vibrant biotech company.  Below are the types of openings available: Summer Internships These positions are typically posted early in the calendar year, by February, and are 40 hours per week.  Most summer internships begin in May or early June and run through middle/late August.       Co-OpsCo-Op positions are full time, 40 hours per week that last close to 6 months, and we hire 4-6 Co-Ops each cycle:<ul><li>Positions posted in February for a July – December Co-Op</li><li>Positions posted in September for a January – June Co-Op.</li></ul> Postdoctoral Research FellowshipsWe will open up these 18 month long positions as needed. Please submit your resume today and we will notify you as opportunities arise!

Visterra, Inc.

Future Intern and Co-Op Openings

Clinical Research

Drug Development

Finance

Human Resources

BioSpace

Environmental Manager

Trinity is seeking an experienced Safety Health Environmental (SHE) Coordinator to work onsite at a client’s Research & Development (R&D) facility, a globally recognized leader in the Biotech industry. Bachelor’s degree in Occupational Safety, Health, and Environment (or equivalent) qualified health and safety professional, or degree in a science, engineering, sustainability or manufacturing discipline.

Trinity is seeking an experienced Safety Health Environmental (SHE) Coordinator to work onsite at a client’s Research & Development (R&D) facility, a globally recognized leader in the Biotech industry. This is a full-time role onsite, where you will be employed by Trinity and eligible for benefits including competitive compensation, comprehensive medical, dental, and Vision, Life insurance, 401K plan, paid time off and paid holidays. You will have the opportunity to support two exceptional companies that are leaders in their space.Essential Job Functions:<ul><li>Participate as an active member of the SHE Team contributing to ensuring the overall delivery of the SHE compliance matters.</li><li>Perform SHE and Sustainability regulatory reviews to establish compliance registry for existing and new operations.</li><li>Modify and develop standard operating procedures associated with federal, state, local and company requirements and guidelines.</li><li>Review existing training material and develop robust modules with in-person, online and ad-hoc capabilities.</li><li>Facilitate management of change and risk assessment execution for ongoing and new projects.</li><li>Develop long-term SHE programs to accommodate business growth and change.</li><li>Participate in cross-functional teams to assess and address SHE compliance matters.</li><li>Develop and maintain key relationships with all site customers.</li><li>Support the site’s environmental sustainability through research, data gathering and project implementation.</li></ul>Essential requirements:<ul><li>Bachelor’s degree in Occupational Safety, Health, and Environment (or equivalent) qualified health and safety professional, or degree in a science, engineering, sustainability or manufacturing discipline.</li><li>2+ years of relevant experience.</li><li>Preferred work experience in a pharmaceutical or biotechnology environment and in developing safe working processes.</li><li>Excellent communication skills and be comfortable supporting stakeholders at all levels.</li><li>Ability to work independently and cascade appropriate knowledge to key stakeholders.</li><li>Strong time management and organizational skills and able to meet deadlines.</li></ul>Desirable requirements:<ul><li>A dynamic approach and comfortable working in an agile environment.</li><li>Experience working in a multi-team environment.</li><li>Good understanding of and approach to risk management.</li></ul> Employment Type: Full Time Years Experience: 1 - 3 years Bonus/Commission: No

Trinity Consultants Engineering & EHS Workforce Solutions

Safety Health Environmental ( SHE ) Coordinator

Business Growth

Change Management

Communication Skills

Cross-Functional

Customer Relations

Data Collection

Environmental Research

Functional Analysis

Online Advertising

Organizational Skills

Regulations

Research & Development (R&D)

Risk Analysis

Risk Management

Safety Process

Safety/Work Safety

Standard Operating Procedures (SOP)

Standards Development

Sustainability

Team Player

Time Management

iHire

Research Scientist

Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney diseases and other hard-to-treat diseases. The ideal candidate should have an advanced degree in immunology, biology, biochemistry or a related field and a minimum of five years (post-graduate) of research experience in a biotech or pharmaceutical setting.

Principal Scientist, Research  Summary Visterra, Inc., is searching for a highly experienced Principal Scientist with a strong background in design and engineering of biologics. The ideal candidate will have experience in leading early discovery stage programs and have a proven track record of success in discovering and developing antibody-based therapies. This individual will lead programs through target identification, target validation, antibody discovery and lead optimization stages. The successful candidate will be a collaborative team player, an effective hands-on manager to junior scientists, a critical thinker, and a clear communicator. The ideal candidate should have an advanced degree in immunology, biology, biochemistry or a related field and a minimum of five years (post-graduate) of research experience in a biotech or pharmaceutical setting. This is a full-time position located at Visterra’s offices in Waltham, MA. At Visterra we are making a positive impact on people’s lives through better medicine with a team that champions innovation, teamwork, and perseverance. Key duties and responsibilities <ul><li>Drive program strategy, lead team through preclinical data acquisition, set program timelines, define and reach go/no-go decisions</li><li>Lead the discovery and engineering of novel biologics in the field of autoimmunity, nephrology, and/or neurology</li><li>Evaluate novel technologies in antibody discovery and molecular biology to enhance and streamline discovery workflows</li><li>Design and lead execution of experiments involving antibody libraries, antibody engineering and antigen characterization</li><li>Independently analyze scientific results, troubleshoot methods and conceive creative solutions and workflows to address challenges</li><li>Document, analyze and interpret data for internal decision making, publications, presentations, patents and regulatory filings.</li><li>Work closely with key opinion leaders to advance Visterra’s research interests and development of therapeutics</li><li>Manage activities at contract research organizations (CROs)</li><li>Effectively communicate research results and program strategies internally and externally, including presentations at scientific forums</li><li>Maintain expertise by actively participating in conferences and staying current with relevant literature</li><li>Includes management of direct reports</li></ul> Minimum Qualifications <ul><li>A Ph.D. or equivalent advanced degree in immunology, biology, biochemistry, or related field and a minimum of five years (post-graduate) of laboratory-based research, preferably in industry</li><li>Strong foundation in understanding of antibody structure and function, roles in immune regulation, and therapeutic applications</li><li>Track record of completing protein engineering projects</li><li>Experience conducting original research in cell biology, immunology, target discovery, or therapeutic mechanism of action</li><li>Ability to design, develop and execute antibody discovery campaigns</li><li>Experience in the screening and characterization of protein-based therapeutics using in vitro and/or cell-based assays</li><li>Strong data analyses skills and solid written and oral scientific communication and documentation skills</li><li>Track record of managing a team of scientists and research associates</li><li>Detail-oriented, organized, team-oriented, enthusiastic and flexible with effective communication skills</li></ul> Management responsibilities: This position includes supervisory responsibilities Travel: Possible travel to local and national conferences   Company: Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney diseases and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs. Visterra is a wholly owned subsidiary of Otsuka America, Inc., which is a U.S. holding company and a wholly owned subsidiary of Otsuka Pharmaceutical Co., Ltd. of Japan. Visterra has approximately 125 employees and is located in Waltham, Massachusetts. Visterra provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Principal Scientist, Research

Analysis Skills

Antibodies

Assays

Biochemistry

Biology

Campaigns

Cell Biology

Conferences

Contract Management

Contract Research Organization (CRO)

Data Analysis

Detail Oriented

Disease

Engineering

Identify Issues

Immunology

Intellectual Property (IP)

Kidney Disease

Medical Treatment

Medicine

Molecular Biology

Nephrology

Neurology

Patent Applications

Patent Statutes

People Management

Presentation/Verbal Skills

Publications

Regulatory Submissions

Research Laboratory

Research Skills

Sales Pipeline

Scientific Publications

Scientific Research

Team Lead/Manager

Technical/Engineering Design

Willing to Travel

Writing Skills

Intellectual Property Attorney

The successful candidate will be capable of managing multiple projects simultaneously in a fast-paced environment, and will possess excellent analytic, legal drafting, and oral and written communication skills. There is no road map for what we are doing as leaders in the systemic delivery of in vivo CRISPR-Cas9 therapies, while offering a full spectrum approach to create CRISPR-Cas9 therapy via our ex vivo pipeline.

Why Join Intellia?Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done.We wantall ofour people to go beyond what is possible. We aren’t constrained by typical end rails, and we aren’t out to just “treat” people. We’re all in this for something more. We’re driven to cure and motivated for change. Just imagine the possibilities of what we can do together.How you will Achieve More with Intellia:Intellia seeks an experienced biotechnology patent attorney to join our legal group in Cambridge, Massachusetts. The attorney will develop and execute a global intellectual property strategy in support of Intellia’s gene editing technology and pipeline programs. We are looking for someone who can work independently to develop and implement solutions, appropriately analyze and manage risks, multitask, and is effective at communicating at all levels of the organization. Most importantly, we seek a team member who thrives in a highly collaborative environment and wants to be fully integrated into every aspect of the company from research to business execution.Responsibilities:<ul><li>Help lead the development of a worldwide IP portfolio covering new IP directed to therapeutic applications of CRISPR-Cas9 genome engineering and delivery technologies.</li><li>Identify patentable inventions through regular interactions with internal R&D project teams, and work with outside counsel to draft, file, and prosecute patent applications worldwide.</li><li>Provide legal advice to internal science, business, and legal teams on a variety of IP related matters.</li><li>Conduct due diligence assessments and counsel based on those assessments, including freedom-to-operate (FTO), infringement and validity analyses, and risk evaluation and mitigation.</li><li>Work on transactions and legal matters supporting Intellia’s research and business goals, such as licensing, collaborations, and other contracts (e.g., consulting, research, service, vendors, manufacturing).</li><li>Analyze trade secret, trademark and copyright issues.</li><li>Assist with challenging and defending patents in PTAB, opposition proceedings, and other forums.</li><li>Interface with key stakeholders, including collaborators, government agencies, consultants, and other third parties. Work on other assigned legal matters relevant to the Company.</li></ul>About You:<ul><li>J.D. degree or LL.M. degree from an accredited law school, admission to practice law in a U.S. jurisdiction, and registered to practice before the U.S. Patent and Trademark Office. </li><li>Minimum of 8-10 years of experience practicing patent or intellectual property law in the life sciences.</li><li>Significant prior legal experience in the pharmaceutical and/or biotechnology fields, with an emphasis on preparation, prosecution, and IP analysis a must.</li><li>Strong preference for advanced scientific degree (Ph.D. or Master’s) in molecular biology, cell biology, biochemistry, chemistry, immunology, genetics, structural biology, or related field.</li><li>The successful candidate will be capable of managing multiple projects simultaneously in a fast-paced environment, and will possess excellent analytic, legal drafting, and oral and written communication skills.</li><li>Experience in all aspects of U.S. and foreign intellectual property law relating to biotechnology, pharmaceutical, or life sciences at a law firm or a biotechnology/pharmaceutical corporation.</li><li>In addition to the basic qualifications listed above, the ideal candidate will have demonstrated leadership, management, and interpersonal skills, and creativity in applying analytical frameworks and solutions to issues.</li><li>Strong client service focus and ability to work independently and in teams, as well as excellent organizational skills, flexibility, and ability to prioritize workflows.</li></ul>Meet your future team:The IP Team is a hard working, highly collaborative team staffed by individuals who value and support each other. We value collaboration, excellence, integrity, and trust. The team functions on a hybrid remote/on-site model that allows for flexibility while fostering a strong sense of community within the team and with stakeholders. Since our team is based in Cambridge, MA, we hope that you are in the Cambridge area.There is no road map for what we are doing as leaders in the systemic delivery of in vivo CRISPR-Cas9 therapies, while offering a full spectrum approach to create CRISPR-Cas9 therapy via our ex vivo pipeline. We thrive on charting new territory, exploring new ways to drive our programs and the business forward. We are cultivating the culture of ONE, EXPLORE, DISRUPT, and DELIVER that has made, and continues to make, Intellia such an incredible place to work.Covid-19 Vaccination Policy:All Intellia employees, regardless of work location, are expected to follow all applicable federal, state, and local public health regulations and guidelines, and are strongly encouraged to follow all public health recommendations, including being vaccinated for COVID-19.EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Intellia Therapeutics

Senior IP Counsel

Chemistry

Consulting

Customer Support/Service

Due Diligence

Editing

Establish Priorities

Genetics

Genomics

Government

IP (Internet Protocol)

Industry/Trade Analysis

Intellectual Property Analysis

International Law

Interpersonal Skills

Legal

Licensing

Multitasking

Patent Procurement

Patents

Project/Program Management

Trademarks

Executive Assistant

Learn more about Beacon Hill and our specialty divisions, Beacon Hill Associates, Beacon Hill Financial, Beacon Hill HR, Beacon Hill Legal, Beacon Hill Life Sciences and Beacon Hill Technologies by visiting www.bhsg.com. Our niche brands offer a complete suite of staffing services to emerging growth companies and the Fortune 500 across market sectors, career specialties/disciplines and industries.

Salary

<img height="1" src="https://counter.adcourier.com/YmF0LjA4NTkyLjQ3OUBiZWFjb25oaWxsLmFwbGl0cmFrLmNvbQ.gif" width="1"/> Our client, a global biotechnology company, is seeking a polished and highly organized Executive Assistant to support a Senior Vice President and a Vice President. This full-time, 100% onsite role is based in Boston, MA and runs through the end of the year, offering competitive pay of $55-$60 per hour. Standard working hours are 8:30 AM to 5:30 PM. Qualified and interested candidates are encouraged to apply today for immediate consideration. Key Responsibilities: <ul><li>Provide high-level administrative support to C-suite executives, managing complex calendars and travel logistics</li><li>Handle sensitive and confidential information with discretion</li><li>Coordinate meetings, prepare agendas, take minutes, and assist with PowerPoint presentations</li><li>Interact with senior leaders and external partners to support executive needs</li><li>Process purchase orders, invoices, and contracts</li><li>Maintain internal communication tools, including the company's internal newsletter and VNET page</li><li>Support onboarding activities and provide guidance to less experienced colleagues</li><li>Anticipate executive needs and proactively streamline administrative processes</li></ul> Candidate Qualifications: <ul><li>Minimum 5 years of relevant experience, preferably in biotech or pharmaceutical industries</li><li>C-suite support experience required</li><li>Advanced proficiency in Microsoft Office (Outlook, Word, PowerPoint, Excel)</li><li>Strong organizational, time management, and multitasking skills</li><li>Excellent verbal and written communication abilities</li><li>Professional demeanor and ability to interact with high-level stakeholders</li><li>Proven ability to manage confidential information with integrity</li></ul> Beacon Hill is an equal opportunity employer and individuals with disabilities and/or protected veterans are encouraged to apply. California residents: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. If you would like to complete our voluntary self-identification form, please <a href="https://jobs.beaconhillstaffing.com/eeoc/" rel="nofollow noopener noreferrer" target="_blank">click here</a> or copy and paste the following link into an open window in your browser: https://jobs.beaconhillstaffing.com/eeoc/ Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records.<a href="http://twitter.com/#!/BHStaffingGroup" rel="nofollow noopener noreferrer" target="_blank"> </a> Company Profile: Founded by industry leaders to set a new standard in search, career placement and flexible staffing, we deliver coordinated staffing solutions with unparalleled service, a commitment to project completion and success and a passion for innovation, creativity and continuous improvement. Our niche brands offer a complete suite of staffing services to emerging growth companies and the Fortune 500 across market sectors, career specialties/disciplines and industries. Over time, office locations, specialty practice areas and service offerings will be added to address ever changing constituent needs. Learn more about Beacon Hill and our specialty divisions, Beacon Hill Associates, Beacon Hill Financial, Beacon Hill HR, Beacon Hill Legal, Beacon Hill Life Sciences and Beacon Hill Technologies by visiting <a href="http://www.bhsg.com" rel="nofollow noopener noreferrer" target="_blank">www.bhsg.com</a>. Benefits Information: Beacon Hill offers a robust benefit package including, but not limited to, medical, dental, vision, and federal and state leave programs as required by applicable agency regulations to those that meet eligibility. Upon successfully being hired, details will be provided related to our benefit offerings. We look forward to working with you. Beacon Hill. Employing the Future (TM)

Beacon Hill Staffing Group

salaryMin

salaryMax

payPeriod

currency

Administrative Skills

Billing

Calendar Management

Continuous Improvement

Executive Assistant Skills 

Fortune 500 Customers

Logistics

Meeting Minutes

Microsoft Excel

Microsoft Office

Microsoft Outlook

Microsoft PowerPoint

Microsoft Word

Newsletter

Onboarding

Plan Meetings

Process Development

Purchase Orders

OTHER

Travel and Tourism

Licensure and/or CertificationActive licensed Pharmacist in the Commonwealth of Massachusetts (or eligible for reciprocity) is required Board CertificationJob SummaryReporting to the Director of Pharmacy Services, the Clinical Pharmacist is responsible for providing pharmaceutical care through the verification, filling and dispensing of medication orders. ExperienceA minimum of 1-2 years of experience in a hospital pharmacy setting is highly preferredCompletion of an ASHP accredited PGY1 residency desirable.

ID: 54313088 Shift: 8hr Days 8x5 Description: HWL Hospital-AN-0324 Travel Rate: $97Local Rate: $89Days with some evenings, no call, no holidays and every 5th weekend.EducationGraduate of an accredited college/university with a B.S. in Pharmacy or a Pharm.D. degree is required.ExperienceA minimum of 1-2 years of experience in a hospital pharmacy setting is highly preferredCompletion of an ASHP accredited PGY1 residency desirable.Licensure and/or CertificationActive licensed Pharmacist in the Commonwealth of Massachusetts (or eligible for reciprocity) is required Board CertificationJob SummaryReporting to the Director of Pharmacy Services, the Clinical Pharmacist is responsible for providing pharmaceutical care through the verification, filling and dispensing of medication orders. Provides clinical services and medication information to medical and nurses ensuring appropriate medication use. Supervises and verifies the accuracy of all work performed by pharma technicians and students. Supports all clinical pharmacy services and initiatives including the pharmacy residency program. Works independently with limited supervision. Develops and promotes collaborative and collegial relationships with medical staff, nurse and other allied health clinical staff Guaranteed Hours: 40 Weekly Contract Weeks:89

Infojini Healthcare

Travel Pharmacist - $2,448 per week in Concord, MA

Clinical Medicine

Clinical Support

Employee Relations

Hospital

Medical Records

Medications

Nursing

Pharmacy

Allied Travel Careers

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