Jobs in Science

Manufacturing Operator 57
Integrated Resources, Inc    02-12-2020 Lenexa, KS, USA

Title: Manufacturing Operator

Location: Lenexa, KS

Duration:6 months


Job responsibilities:

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 weight.
  • Use a computer to capture production information.
  • Approve related reports and complete related documentation.

Blending and Milling Tasks:

  • Check rooms and equipment for cleanliness and damage prior to use.
  • locate formulated chemicals for charging into blenders.
  • setup and operate blenders in accordance with required specifications.
  • setup and operate pin mill system in accordance with required specifications.
  • setup and operate nitrogen conveying system.
  • setup and operate clean-in-place (CIP) systems.
  • control and monitor processes with an operator interface terminal (OIT).
  • use a computer to capture production information.
  • approve related reports and complete related documentation.

Packaging Tasks:

  • Use designated weights from 1 gm to 25 kg to verify scales are in specification.
  • Confirm material and supplies are staged.
  • Set up and operate automated packaging equipment within specified tolerances.
  • Fill powder into final containers up to 100 kg in weight.
  • Perform label reconciliation to ensure proper package labeling.
  • Move pallets of product to finished goods storage.
  • Approve related reports and complete related documentation.
  • Must be able to properly gown and comply with all cGMP and PPE guidelines
  • Set-up equipment ensuring operations are consistent with current operating procedures.
  • 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 SOP's,
  • Work Instructions and Master Batch Records (MBR).
  • Completes all documentation in accordance with current Good Manufacturing Practices (cGMP) and SOP.
  • Perform operations in compliance with rules and in a safe, orderly manner.
  • Participates in training programs as directed by the Department Supervisor.
  • This may include monthly safety meetings, internal safety audits of operations, respirator training, and skill-based pay.
  • Follow production procedures and safety policies at all time.
  • 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
  • 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.


Knowledge and Skills

  • 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.


Soft Skills

  • Works as a productive member of a team
  • Ability to effectively communicate with others.
  • Basic mechanical aptitude
  • Basic problem solving


Skills Required:

  • Must be able to lift 5 pounds for a six-hour period, or as required.
  • Occasionally required to lift up to 50 pounds.
  • Must be able to maneuver and position mechanical components up to 50 kg.
  • Must be able to stand for long periods of time
  • Must be able to work within a controlled space without excessive perspiration



Scientist IV 54
TekWissen LLC    12-19-2019 Rockville, MD, 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 research and development, manufacture and sale of products in the health care field. 

It also operates through the segments such as Consumer, Pharmaceutical, and Medical Devices.





Key Responsibilities:

• The majority of your time will be spent in the laboratory conducting and participating in complex and scientifically demanding projects to build oncolytic herpesviruses within the framework of a small team.
• You will design and implement laboratory experiments under the mentorship of a Senior Scientist and provide high quality data in a timely fashion, including drafting and executing technical reports.
• You will present at group meetings and provide materials/slides for senior scientists at project or unit presentations.


• A Master’s Degree in Biological Sciences with at least six years of experience or a recent PhD with at least 3+ years (post-PhD) research experience in molecular virology or molecular biology
• Can design, execute and interpret in vitro studies with some supervision
• Ability to mentor less experienced co-workers
• Ability to handle multiple projects in a dynamic environment
• Experience in genetic design and molecular manipulation of HSV-1 or Vaccinia is preferred.
• Experience with genetic recombination and modification of large DNA constructs is preferred.
• Experience with recombinant antibody design is a plus but not required.


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


Statistician Scientific III 44
TekWissen LLC    12-16-2019 Fort Washington, PA, 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.  


  • Subject Matter Expert (SME) in the use of non-clinical mathematics/statistics supporting an assigned review of GMP and non-GMP documents (e.g. protocols, reports) to ensure the appropriate use of mathematics, statistics and/or graphical tools and interpretation.  
  • Assigned projects to the role may include the application of statistical/mathematical approaches for innovation, development, commercialization, validation and life-cycle management of drug product manufacturing and packaging processes including solid (e.g., tablets, caplets, …) and non-solid (e.g., solutions, suspensions, ointments, …) dosage forms. The assigned tasks will be heavily focused on techniques associated with descriptive, inferential, predictive, prescriptive, and/or causal analysis.

  • Bachelor’s Degree required 

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

Associate Scientist - I 55
TekWissen LLC    12-16-2019 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.
Specific Responsibilities:
  • We are seeking a highly motivated, creative, and collaborative individual with a background in immuno-oncology and/or immunology to support the development of novel therapeutics.
  • This individual will be part of a cross-functional team within the Immuno-oncology group. 
Primary responsibilities will include: 
Designing, validating and performing novel cell-based immunology assays; screening and evaluating potential lead drug candidates; interpreting results, proactively troubleshooting technical challenges and recommending potential solutions based on personal observations and/or literature searches. The work will be conducted in a highly interactive and collaborative multi-disciplinary scientific environment.
Essential Duties and Job Functions:
  • Plans and executes experiments that support research activities and project goals. 
  • Demonstrates and applies a high level of understanding of project goals and methods. 
  • With general guidance and direction selects appropriate methods and techniques in performing experiments.
  • Recommends creative solutions to problems, researches new methods and techniques and may proactively seek out senior personnel to discuss potential solutions to problems. 
  • Works with limited to minimal supervision on projects of moderate scope and complexity. Participates in group meetings. 
  • Clearly presents results of work, interprets data, and draws conclusions regarding presented material and nature of work.
Knowledge, Experience, and Skills:
  • Typically requires a BS/BA degree in Immunology, Microbiology, Molecular and Cell Biology or other related life science disciplines and a minimum of 5+ years of relevant experience. 
  • The ideal candidate will have hands-on experience in one or more of the following techniques: immune cell functional assays, multi-color flow cytometry, primary cell isolation and culture, ELISA/Luminex/MSD, and cell line maintenance including culture and preservation. 
  • The candidate should be a creative and goal-oriented problem solver capable of working independently. 
  • The candidate must be able to process data and evaluate data quality, including recognizing anomalous and inconsistent results. 
  • The candidate should have mature organizational skills, strong verbal and written communication skills and the ability to work effectively in cross-functional teams.
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
How many years of Associate Scientist experience do you have?
How many years of cell isolation and culture, ELISA/Luminex/MSD experience do you have?
Microbiologist 78
Integrated Resources, Inc    12-13-2019 Vernon Hills, IL, USA

Job Title:               Microbiologist
Work Location:  Vernon Hills. IL.

Duration:             12 Months (Possibility of Extension)


Performing, with little or no oversight, a variety of tasks related to microbiological testing of products and raw materials.

  • Performing routine and some non-routine USP, ASTM and CLSI based microbiological testing for anti-infective and disinfectants.
  • Providing assistance to scientific staff to support current commercial products and line extensions by providing scientific review, investigation and support according to the established product development process and quality procedures.
  • Managing and maintaining every aspects of the microbiology laboratory to provide material and technical support to all microbiology staff members.
  • Writing study protocols and SOPs.
  • Preparing study reports and protocol completion summaries.




BS degree in Biological Sciences or Microbiology



  • Applies working process knowledge in resolving routine problem/issues
  • Coordinates problem resolution with supervisor as needed
  • With moderate or no supervision, applies comprehensive understanding of defined productivity goals and objectives
  • Applies knowledge and skills to complete assigned tasks within own area
  • Works within established SOPs and / or scientific methods and adheres to quality guidelines
  • Performs general laboratory duties such as preparing media, reagents and re-stocking supplies, and/or propagating important microbial cultures.
  • Performs routine microbiological assays such as ISO, USP and ASTM-based microbiological testing of products.
  • Maintains and propagates bacterial culture, and perform identification based on Gram stain and morphological characteristics
  • Uses theoretical knowledge to interpret data and to trouble-shoot experiments. Independence in problem-solving is highly encouraged.
  • Prepares and presents data at laboratory meetings.
  • Becomes more independent in planning and conducting experiments, and collaborates with scientists from other sections of the R&D organization.
  • Reports any incidence or malfunction of equipment in the lab
  • Assures that all aspects of their assigned areas are secure and maintained in accordance to all applicable procedural requirements
  • Performs other duties as assigned by management



  • Minimum 1 year of work experience in a Microbiology Research & Development Environment or equivalent combination of education and experience
  • Specialized Knowledge
  • Ability to read, analyze, and interpret technical procedures or governmental regulations
  • Mathematical and reasoning ability: Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
  • Ability to work with colleagues and multiple clients in a professional and organized manner, and interact effectively with a variety of people from different nationalities, ethnic/cultural backgrounds, and educational levels.
  • Should be able to define problems, collect and interpret data, establish facts, draw valid scientific conclusions, and propose solutions or corrective actions
  • Ability to organize and prioritize work with limited guidance and to manage projects in a timely and effective manner.


Manufacturing Technician 68
Integrated Resources, Inc    12-10-2019 Lexington, MA, USA

Title: Manufacturing Technician

Location: Lexington, MA

Duration: 06 Months+



Performing cell culture sterilization techniques, support mammalian cell culture manufacturing processes, sustaining purification of biopharmaceuticals, operate various process equipment, documenting daily manufacturing operations in a cGMP environment, working with bioreactors, experience in upstream or downstream manufacturing, fermentation, and/or filtration, executing validation protocols


Microbiologist 82
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 87
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 61
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 92
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.


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