Jobs in Science

Microbiologist 2
Integrated Resources, Inc    12-06-2019 Malvern, PA 19355, USA

Title: Microbiologist

Location: Malvern, PA

Duration: 12 Months+  



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. 
Bachelor’s degree required.


Chemist 6
Integrated Resources, Inc    12-03-2019 Titusville, Hopewell Township, NJ 08560, USA

Title: Chemist


Duration: 12 Months+



The Chemist-I conducts analytical testing of stability samples submitted to the QC laboratories according to testing schedules in a productive and efficient manner.

This position requires testing to be completed in compliance with all applicable procedures, standards and GMP regulations as well as all local, state, federal and international regulations and guidelines (FDA, EPA, DEA, OSHA, etc.)
Additional tasks, duties, and responsibilities include utilizing electronic systems (LIMS, Empower, etc.) for execution and documentation of testing, sample and reference standard management, maintaining individual training completion in a compliant state, completing corrective and preventative actions (CAPA) as assigned, supporting the investigation and resolution of laboratory nonconformances, general housekeeping and other duties as assigned by management.

This role requires a minimum of a B.S. degree in a scientific field and a minimum of 1-2 years’ experience working in a GMP laboratory environment.

Required skills, knowledge and ability for this role include;
-knowledge and experience with analytical technologies used in a QC Laboratory (HPLC, FT-IR, dissolution, UV/Vis, etc.)
-knowledge and understanding of current Good Manufacturing Practices (cGMP)
-Ability to read and interpret documents such as SOPs, work instructions, test methods and protocols
-Basic troubleshooting and root cause analysis skills.


Scientific Support 5
Integrated Resources, Inc    12-02-2019 Ashland, OH 44805, USA

Job Title: Scientific Support  

Duration: 6 Months

Location: ASHLAND, OH



  • Provides administrative, logistical and technical support for Scientific staff conducting studies or supporting functions for operations of the laboratory.
  • Coordinates all laboratory support, pre-study activities, method development, method validation, study activities, data and/or reporting activities.
  • Responsible for data review for completeness, quality or QC against the applicable protocol or procedure.
  • May be responsible for drafting client correspondence, study correspondence, reporting or direct client interaction.
  • Interacts with other departments, scientific staff, and sponsors either locally or across sites.



Quality Control Research Associate 16
Integrated Resources, Inc    11-27-2019 Gaithersburg, MD, USA

Job Title : Quality Control Research Associate 

Duration : 6 Months (Possibility of extension)

Location : Gaithersburg, MD


Job Responsibilities::

  • Conducts routine analyses based on written procedures
  • Reviews data and results of testing to ensure compliance to appropriate specifications and protocols.
  • Performs maintenance and calibration of analytical instrumentation.
  • Begins to learn and apply knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Practices (GLPs) on a daily basis.
  • Writes simple protocols and reports.
  • Must have working knowledge of Microsoft Office software.
  • Participates in group meetings.
  • May present data or prepare information for others to present.


Manufacturing Associate 27
Integrated Resources, Inc    11-27-2019 Chaska, MN 55318, USA

Job Title : Manufacturing Associate
Duration : 12 Months (possibility of extension)
Location :
Chaska, MN


Essential Duties/Responsibilities:

  • Assemble various types of electro-Mechanical sub-assemblies.
  • Assemble cables, Tubes, and wiring harnessing.
  • Following all assemblies documented procedure.
  • Follow company DHR, GMP, SOP, QSR, and adhere to company quality procedures and policy.
  • Train on latest revision of procedures and work instructions as well as update on training for best performance on quality products.
  • Follow Company Safety Policy.
  • Have good understanding and be knowledgeable on Good Manufacturing Practice.
  • Maintain a Clean and Organized work area.
  • Good Hand Dexterity.
  • Complete all inventory transactions and assemble packaging.



  • High School Diploma, Requires a minimum of one year current electro-mechanical assembly experience.
  • Read assembly drawings, bill of material, follow assembly instructions and schematics written in English.
  • Operate various types of hand tools.
  • Experience in QSR or ISO environment


Scientist-I/ Cell Culture/ Tissue Culture 10
TekWissen LLC    11-25-2019 San Diego, CA 92121, USA


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 biotechnology product development services. The Company focuses on providing laboratory equipment, chemicals, supplies and services used in healthcare, scientific research, safety, and education. 



Job Description: 

  • Scientist- l will work in the Predictive and Investigative Toxicology group.
  • S/he will tactically support collaborative, hypothesis-driven risk assessment of compound-related toxicity using broad knowledge of biochemistry, anatomy, physiology, molecular biology, immunology, neuroscience, pharmacokinetics, and toxicology. 

Required experience/skills:  

  • Cell culturing [primary, stem cells] 
  • RNA,DNA and protein extraction/quantification from cells/tissues/biological fluids/cell culture media samples 
  •  PCR (mRNA, microRNA) analysis 
  •  Western blot analysis 
  •  ELISA, Multiplex (e.g. Luminex, Mesoscale) immunoassays 
  •  Immunocytochemistry 
  •  cell imaging. 

Desired experience/skills:  

  • Safety Biomarkers 
  •  Flow cytometry 
  •  Organ-on-chip (e.g. kidney) 
  •  RNA-Seq 
  •  Proteomics 
  •  and/or In vivo study conduct. 
  • S/he will perform assigned tasks with limited supervisor’s assistance 
  •  provide input/identify problems with lab experiments 
  • order supplies 
  •  generate study protocols and data tables in Excel, PowerPoint and/or Word 
  • record experimental methods/data in an electronic database/lab notebook 
  •  analyze data using statistical packages (e.g. GraphPad Prism) 
  •  communicate (verbal, written) results 
  •  and draft technical reports in a timely manner. 


  • A minimum of a B.S./B.A. degree (with 4 years of experience) 
  •  M.S. degree (with 3 years of experience) or Ph.D. (with 2 years of experience) in performing progressively advanced research within a pharmaceutical research and development environment is required. 
  • This job requires an ability to develop the knowledge and application of corporate policies/guidelines /standard operating procedures, local, state and federal guides, laws and regulations. 

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

Lab Technologist 12
Integrated Resources, Inc    11-25-2019 Austin, TX, USA

Job title: Lab Technologist

Location: Austin, TX

Duration:6 months (Possibility of extension)


Job Responsibilities:


  • Execute product manufacturing according to established procedures, record the data, interpret results and validate the quality of the data.
  • Perform in-process and/or final quality control testing and accurately document all results.
  • Perform lab calculations needed to make solutions from powder or from stock solutions.
  • Support general lab functions, setup, calibration and maintenance of equipment. Production records will be reviewed by senior production staff or supervisor.
  • Perform transactions using ERP or equivalent system. Accurate and reliable inventory management participation.
  • Achieve high productivity while maintaining all quality standards.
  • Organize and prioritize work to ensure on-time delivery. Periodically review and discuss your priorities with supervisor.
  • Critically think about the manufacturing process and suggest improvements to maintain high quality standards.
  • Actively participate in process improvement projects.
  • Adherence to ISO guidelines and the quality policy.
  • Actively participate in maintaining a safe, clean, and functional work environment. Responsible for the completion of all tasks assigned daily; this may require more than 40 hours in some work weeks.


Additional Responsibilities:

  • Work may involve the handling of hazardous or biological materials.
  • Must have adequate training to safely handle these materials and work safely under laboratory rules and SOPs.
  • May include labeling, dispensing, packaging of reagents and final product.
  • Participate in the investigation, recording and implementation of product deviations or CAPA systems.
  • Participate in transfer and implementation of new products into the production lab.
  • Other duties as assigned.


Qualifications: Associate or B.S. degree in Life Sciences, or related scientific discipline with 0-3 years of job related experience.


Knowledge, Skills &Abilities:

  • Familiarity with common equipment such as plate readers, centrifuges, balances, and liquid transfer equipment.
  • Experience or knowledge of assays such as ELISA and Lateral Flow.
  • Pipette reproducibly. Basic lab and computer skills. Attention to detail and follows instructions.
  • Ability to work in a fast paced environment and willingness to cross-train in multiple areas within the operations group.
  • Effective communicator (verbal and written). Proactive, hardworking and self-motivated.
  • Follow directions and instructions accurately.
  • Address and report to supervisor any problems in daily manufacturing and propose effective countermeasures.


Engineer Scientist 27
Integrated Resources, Inc    11-25-2019 Fremont, CA, USA

Job Title: Engineer Scientist/QC

Location: Fremont, CA

Duration: 6 Months



  • Using (SOP) standard operating procedures and (GMP) good manufacturing practices, the Chemist will perform routine testing of raw materials, work-in-process materials, finished goods kits, and filled bottle components.
  • The QC Engineer/Scientist I will be responsible for all aspects of laboratory operations, such as sample receipt, data generation, product verification, data analysis and summarization, out-of-specification investigations, instrument qualifications, and all other QC lab supporting activities.


Job Description:

  • Conducts analytical and functional testing of raw materials, intermediates, finished goods kits and/or filled bottle reagents/calibrators according to approved SOPs.
  • Perform testing using chemistry clinical analyzers and document accurate test results using spreadsheets and workbooks.
  • Performs initial troubleshooting of issues which arise during routine analysis, perform out of specification OOS investigations and if needed, initiate non-conformance NCAR reports.
  • Documents test results, complete batch records, document problems and other relevant information under cGMPs.
  • Performs simple revisions and updates to SOPs as necessary and initiate procedure change orders.
  • Summarize test data, maintain lot histories and analyze data for trends and discrepancies.
  • Maintain and order lab supplies as needed, and participate in lab clean ups.
  • Participates in interdepartmental and team meetings.
  • Performs other responsibilities to support the needs of the department as assigned by Supervisor.

Education and Qualifications:

  • Minimum BS/BA in Chemistry, Biochemistry, or Bioscience with 0-2 yrs Quality Control experience, preferably in the medical diagnostics industry.
  • Strong laboratory skills including pipetting, safety, and hazardous chemical handling.
  • Understanding of cGMP and how it applies to the work environment is preferred.
  • High level of reading comprehension skills.
  • Ability to follow written and verbal directions with a high level of accuracy.
  • Must be able to write clear, understandable documentation.
  • High level of verbal communication skills.
  • Manual dexterity, must be able to lift/move up to 20 pounds.
  • Intermediate word processing and spreadsheet software skills.
  • Ability to manage multiple tasks simultaneously.
  • Ability to work independently.
  • Ability to perform simple data analysis and to summarize results.
  • Basic math skills including calculation of concentrations and dilutions and a strong grasp of algebraic concepts.



Manufacturing Operator 24
Integrated Resources, Inc    11-18-2019 Haverhill, MA, USA

Job Title: Manufacturing Operator

Work Location: Haverhill MA

Duration: 6+ months (possible extension)


  • High School Diploma / GED.
  • 2+ years' experience in an industrial setting with thorough knowledge of safety procedures relating to chemical handling.
  • 1+ year experience or skill in SAP or similar software such as ERP or MRP systems.
  • Performs production procedures in accordance with Standard Operating Procedures (SOP), resulting in quality product.
  • Formulation Tasks: Gather chemicals from different storage locations (i.e. room temperature, coolers and freezers); use designated weights from 1 gm to 250 kg to verify scales; scoop and dump chemicals into containers up to 1,000 kg; place finished containers on a scale to verify gross weights; use a computer to capture production information; approve related reports and complete related documentation.
  • Equipment components can weigh up to 50 kg and have critical tolerance requirements.
  • Report equipment failures and work with repair personnel to correct problems
  • Performs procedures resulting in the cleaning of manufacturing equipment and facilities.
  • Continually increases proficiency and understanding of manufacturing processes and systems.
  • Able to Read and understand all written procedures as outlined in SOPs, Work Instructions and Master Batch Records (MBR).
  • Completes all documentation in accordance with current Good Manufacturing Practices (cGMP) and SOP.
  • Maintain good housekeeping in working areas.
  • Reports any unsafe working conditions or safety concerns through the corporate Medgate system.
  • Reports any property damage to the shift supervisor immediately
  • Takes part in and contributes to a safe working environment by following corporate and departmental safety regulations. Use, clean, and store all personal protective gear appropriately
  • Makes recommendations for continuous process improvements in the manufacturing area. 
  • Actively participates in Quality systems practices.



  • High school diploma or equivalent with good math and reading skills.
  • Experience in a manufacturing environment preferably with cGMP or regulatory compliance practices. Demonstrated mechanical aptitude including previous maintenance experience with process equipment or mechanical systems. Dry product processing and packaging experience.
  • Ability to read and follow written and verbal instructions.
  • Ability to perform basic metric and other mathematical calculations.
  • Ability to work independently and as part of a team.



Scientist II 17
TekWissen LLC    11-14-2019 South San Francisco, CA, USA


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 biotechnology product development services. The Company focuses on providing laboratory equipment, chemicals, supplies and services used in healthcare, scientific research, safety, and education. 


Job Description 

  • The successful candidate will support new product initiatives and sustaining released projects within the Molecular Biology R&D team.  
  • The candidate will apply molecular biology laboratory skills for the proper execution of Ion Torrent DNA sequencing, collect and analyze data, and present results. 
  • This position entails working with a team of experienced scientists and interaction with cross-functional teams.    


Minimum Requirements:  

  •  B.S. in molecular biology, chemistry or similar disciplines. 
  •  1-8 years of experience in molecular biology or DNA sequencing industry 
  •  Experience in the nucleic acid analysis including PCR amplification and purification. 
  •  Experience in the optimization of reagents and protocols.  
  •  Excellent organizational, record keeping and communication skills.  
  •  A strong work ethic to deliver results in a fast-paced, collaborative environment is necessary. 


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