Jobs in Biotech

Quality Control Microbiology Tech - I 2
TekWissen LLC    12-06-2019 El Segundo, CA 90245, USA
Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is to one of Our clients who offer a biotechnology company that researches, develops and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.

 

  • Maintains lab areas in a clean, orderly, and sanitized state. 
  • Performs environmental and/or utility monitoring and sampling as a primary function. 
  • Receives, quarantines, and stores purchased microbiological media pending laboratory release. 
  • Monitors biohazardous waste and coordinates its removal with qualified safety personnel. 
  • Wraps and prepares equipment for sterilization. 
  • Maintains the lab areas in a clean, orderly, and sanitized state. 
  • Participates in validation and commercial/developmental manufacturing activities as required.
 
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
 
Questions:
 
  1. How many years of lab technician experience do you have?
Microbiologist-I 4
TekWissen LLC    12-06-2019 Malvern, PA 19355, USA

Performs qualitative and quantitative chemical/microbial analysis of in-process manufacturing materials. 

·         Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow.

·         Functions as a team member in the QA Microbiological Laboratories to provide timely test analysis information on the status of conformance to requirements.

·         Investigates testing abnormalities and implements corrective action. 

·         Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. 

·         Assists with determination of root causes of non-conformances and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance.

·         Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required.

·         Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. 

·         Audits documentation, device history records, and test methods for compliance. 

·         This position will be Sunday-Thursday 1st shift including occasional holidays.

·         1st shift 8am - 4pm Sun - Thurs

 

Education:

 

·         Bachelor’s degree required

 

TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity. 

Associate Scientist–Biology I 5
TekWissen LLC    12-04-2019 Foster City, CA, USA
Overview:
 
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is to one of Our clients who offer a biotechnology company that researches, develops and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.
 
Job Description
 
  • We are seeking a highly motivated Associated Scientist to join our Immuno-Oncology group.
  • The selected candidate will be responsible for evaluating novel oncology therapeutics candidates/approaches in pre-clinical animal models to inform diagnostic hypotheses and clinical decision making for experimental and clinical-stage drug candidates.
  • Hands on experience and substantiated knowledge with preclinical mouse models is required.
  • While oncology expertise is a plus, candidates with expertise in pre-clinical models for other diseases models are encouraged to apply.
  • The successful candidate will be proficient with the basic in vitro laboratory skills and familiar with ex vivo sample processing and analysis.
 
Qualifications
 
  • Applicants should have training in a relevant field (BS or MS) with a minimum of 3 years of post-graduate hands on experience or demonstrate equivalent work experience in murine models of cancer, inflammation and/or immunology. Relocation will not be provided for this position.
  • Candidates should have experience in the design, execution and analysis of immunological, tumor, and/or pharmacokinetics/pharmacodynamics (PK/PD) studies.
  • Proficiency in murine handling techniques such as IV, IP, oral dosing, in life and terminal blood collection, and handling of tissues during necropsy and processing for ex vivo analysis is critical for this role.
  • Experience with tissue culture, flow cytometry, ELISA, and molecular biology including genomics and cDNA library preparation, single cell RNA sequencing, and Nanostring will be useful.
  • Excellent communication skills and the ability to work as part of a team is essential.
 
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
Bioinformatics Scientist - IV 4
TekWissen LLC    12-04-2019 Foster City, CA, USA
Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is to one of Our clients who offer a biotechnology company that researches, develops and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.
 
Associate Scientist – Bioinformatics
 
Specific Job Responsibilities
  • With guidance, conduct analysis of large data sets from second and third generation sequencing platforms (Illumina and PacBio).
  • Coordinates transfer and storage of data produced by collaborators or CROs.
  • Develop, maintain, and document data visualization methods tailored to the needs of specific experiments.
  • Create innovative solutions to increase speed and accuracy of data analysis pipelines.
  • Present regular updates to project teams.
  • Can work independently to provide technical solutions to a wide range of difficult problems.
  • Systematically tests and benchmarks bioinformatic software algorithms that may be used in house.
  • Demonstrate the ability to organize, prioritize, and coordinate multiple projects and meet timelines
  • Uses strong communication skills (both verbal and written) and interpersonal skills to communicate objectives and results to biologists, chemists, and non-scientists.
 
Specific Education & Experience Requirements
  • Master’s degree +3 years of experience in bioinformatics, computer science, computational biology, genomics, or a related field. PhD preferred.
  • Proficient in object-oriented programming and algorithm development using R and/or Python.
  • Proficient in GUI development and data visualization.
  • Hands-on experience with Linux/Unix platforms, high-performance computing environment, and version control with Git.
  • Experience with analysis of next generation sequencing data using open source software (e.g. GATK, STAR, BWA) is essential.
  • Familiarity with long-read sequencing (e.g. PacBio) data , R Shiny, and Bioconductor is preferred.
 
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
 
Questions:
  1. How many years of  bioinformatics/computational biology experience do you have?
  2. Do you have experience with Linux/Unix platforms, high-performance computing environment?
  3. Do you have Experience with analysis of next generation sequencing data using open source software?
Validation Engineer 107
ASK IT Staffing    09-11-2019 Bridgewater Township, NJ, USA

Job Description:

Job Title: Validation Specialist

Location: Swiftwater, PA

Duration: 4 Months with possible extension

 

Client has openings to support validation activities at Swiftwater site. The Validation Specialist will be responsible for generating development / validation protocols and reports, and analyzing data for adherence to established acceptance criteria.

 

Skills:

Skills, MS Office 2010, eDoc/GEODE+, Pharmaceutical Validation, Bio Pharma Validation, Validation execution,

 

Technical writing abilities and excellent time management. Strong root cause analysis skills with cGMP experience. To be able to establishworking relationships withother support and production areasin order to gather all of the necessary information required.

 

Must be proficient in eDoc/GEODE+ with a working knowledge of templates, workflows and approval process

Proficient in MS Word, Excel, Powerpoint and Outlook

Interact well with a diverse group of individuals

Self-motivated and willing to be pro-active in resolving issues

Excellent Verbal and written communication skills. Ability to work in a team environment.

 

Process and Automation Engineer 76
ASK IT Staffing    09-11-2019 Allston, Boston, MA 02134, USA
Validation & Verification Engineer/Research Associate 108
Idexcel    08-21-2019 San Jose, CA, USA

Position Title: Validation & Verification

Location: San Jose, CA 95131

Client: Beckton & Dickinson

Pay Rate: $50/hr on W2 all Inclusive

Duration: 12 months (Project will extend according to the candidate performance and Clients need)

 

 

Senior Systems Verification Engineer

To ensure that our cell analysis products deliver outstanding performance and exceed our customers expectations, BD Biosciences is seeking a passionate and capable Senior Systems Verification Engineer to contribute to a cross-disciplinary product development team.

The Senior Systems Verification Engineer participates in the definition, design, and execution of verification activities in the sustaining phase of the product development process for BD Biosciences systems. This includes the design of test methods and test strategies, development and execution of formal protocols, analysis and interpretation of results, and communication of results and their impact through written reports, design reviews, and interactive discussions.

 

 

Primary duties include:

Lead the definition, design, and execution of verification activities in the sustaining phase of the product lifecycle

Represent the department on collaborative projects by elevating customers need and product quality

Exercise independent judgment and apply solution thinking, problem solving, and troubleshooting

Conduct representative sample prep and flow cytometry experiments to test products

Maintain up-to-date knowledge of customer workflows, scientific advancements in flow cytometry, and the competitive landscape

Mentor and support more junior members in understanding systems verification best practices

Escalate top issues by providing clear, well-structured, high-level updates

 

 

Minimum Qualifications: Education and Experience:

B.S. in Immunology, Cell Biology, Engineering or related discipline

Minimum of 5 years' experience in academic research, pharma industry, contract research organizations, clinical research, or other relevant industry.

Minimum of 2 years experience in systems verification principles or studies.

Extensive hands-on experience operating and troubleshooting flow cytometers.

Experience with sample prep and experiment design for multi-parameter flow cytometry applications.

Ability to meet technical objectives and solve challenges under conditions of ambiguity and rapid change.

Experience training bench-level personnel and leading projects.

Excellent listening, written, and oral communication skills.

 

Assets:           

MS or Ph.D. degree in Immunology, Cell Biology, Engineering or in a related discipline.

Strong knowledge of flow cytometry applications.

Research Associate II 150
Integrated Resources, Inc    07-26-2019 New York, NY, USA

Job Title - Research Associate II
Work Location: New York - NY
Duration: 12 Months
Level II position

Need candidate with :
-HEOR experience
-Pharma/Biotech Industry
- Health Economics and Outcomes Research Intern

Role Summary:
This is a full-time 12- 18 month research associate position in the Patient and Health Impact (PHI), Health Outcomes Research (HEOR) team supporting the Hospital Business Unit (HBU) in Client's location The RA will help develop and execute the Global Product Strategy alongside their sponsor and the cross-functional Asset Team(s). The RA will support one or more health outcomes projects that are aligned with the product strategy and value proposition.

Responsibilities:

• Provide support to develop and execute the Global Outcomes Research Product Strategy to support and communicate the value propositions of treatments
• Assess and interpret relevant literature to communicate key findings and/or gaps to internal stakeholders
• Contribute to the development and maintenance of comprehensive global tools such as dossiers (Global Value Dossiers and AMCP dossiers), health economic models, etc. to support optimal pricing and market access
• Assist in the planning and conduct of HEOR studies (including real world evidence studies) to characterize burden of disease to support the unmet medical needs or to address gaps in clinical and economic value
• Facilitate the generation of publications to communicate study findings in scientific channels in alignment of product publication strategy
• Prepare reports and presentations to communicate strategic plans, study findings, project deliverables, and general updates
• Execute and manage projects with external collaborators/vendors to ensure timely completion and quality of deliverables as well as budget/legal and Client's SOP compliance
• Provide support across products and team members in the PHI HBU, as well as cross-functional (Medical, Commercial, Corporate Affairs) support and communication as necessary
• Support management of allocated project budgets to align with priorities and spend forecasts, including tracking invoices and updating internal budget systems

Qualifications:
Education and Knowledge Base
o A masters or PhD degree is required in one of the following: epidemiology, health services research, public health, health economics, or equivalent graduate degree.
o Basic competence with methodological approaches and tools in health services research is required, e.g., literature review, clinical data interpretation and claim data analysis
• 1-2 years of relevant post-graduate professional experience desired for MSc students
• Knowledge of data science and/or health economic methodologies desirable
• Knowledge of international health systems, health technology assessment and pharmaceutical economics preferable
• Experience with using Microsoft Excel and PowerPoint
• Excellent oral and written English communication skills required
• Ability to manage multiple projects involving complex processes, significant budget, competing deadlines and rapidly shifting priorities in a compliant manner
• Ability to operate effectively a fast-paced, a matrix environment
• Successful candidate should be willing to learn, be adaptable, and be proactive

What is the minimum education experience required?: Master's

SCCM Engineer 278
Ampstek LLC    05-31-2019 Folsom, CA, USA

Job Description:

 

  • Good Knowledge of Upgrading and Updating SCCM to supportable CB versions. Ability to help migrate SCCM 2007, 2012, 2012 R2, 2016 to latest supportable CB version.
  • Exposure to deployment and migration tools like MDT and Integration of MDT with SCCM as well as other industry standard SOE and Imaging tools..
  • Provide end to end solution and architecture to build SCCM based on the customer requirement
  • Strong SCCM administration including Microsoft patching, software deployments and Intune integration. Monitor key components and services to maintain software deployment, asset tracking, configuration management, software metering, and Microsoft and third-party patching
  • Should be able to install and configure proxy, transmitter server and deployment server.
  • In-debt knowledge of OSD in general and task sequences in particular.
  • Expertise on supported Windows Operating Systems. Windows 7, 8x and migration from each to Windows 10.  Knowledge of user data migration and related technologies and strategies. Windows 10 Image requirements gathering from Customer considering business requirements, functional requirements and technical requirements. Prepare, Design, Build and rollout Windows 10 SOE on par with industry standards
  • Knowledge of Application rationalization, packaging and deployment. Resolving application issues such as DLL conflicts, registry settings. Familiarity with testing Applications in environments to include Windows 7, Windows 8 and Windows 10
  • Basic Knowledge on SQL Administration and SQL Queries OSD (Operating System Deployment and Imaging)
  • In-depth knowledge of Active directory, ADFS, DFSR, DHCP, AD Certificates & DNS and how it relates to SCCM.
  • Communication and analytical skills. Ability to document articulately the installation process and all configuration information related. Present\whiteboard technical solutions to all levels of an organization. Mentor and provide technical expertise to team members.
Jr Testing Specialist / QA / Tester 241
USA Infotech Inc    05-31-2019 Fairmont, WV 26554, USA

Junior Testing Specialist

Location: Fairmont, WV

Contract and Full Time position

Positions - 6  

 

Primary duties may include, but are not limited to:

 

  • Review documentation to understand testing requirements, test environments and objectives
  • Use standardized testing methods, tools and procedures to ensure testing is efficient, effective and comprehensive
  • Translate requirements into detailed test plans and test cases
  • Execute manual/automated test cases and collect evidences
  • Perform tests in terms of functionality, integration, End-to-End and Regression
  • Document defects identified during testing.
  • Work with users to support User Acceptance Testing
  • Raise outstanding issues through established project management channels, as per project plan

Required Skills:

  • Bachelor's degree in engineering, computer science, business administration, software engineering or related field
  • 2 years of experience with establishing comprehensive test practices and methodologies
  • Possess strong technical skills to build advanced SQL Statements
  • 1 plus years of experience working with Test Management tools like Confluence, JIRA and HP ALM
  • Experience working on Waterfall and Agile development models.
  • Experience in writing and manually executing test cases.
  • Strong analytical skills with attention to detail
  • Ability to think abstract – “outside the box”
  • Ability to handle overlapping assignments

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