Role: SFDC Admin
Duration: Long Term
Location: Durham, NC
Interview Mode: F2F
Need those who can come for F2F Interview
Client's business problem to solve:
Day to Day job Duties:(what this person will do on a daily/weekly basis)
Basic Qualifications: (what are the skills required to this job with minimum years of experience on each)
Travel: It is 100% onsite job from 8 am to 5 pm and travel is not required.
Degree: Bachelor’s in computer science or equivalent work experience in information Technology.
Nice to Have; (But not a must)
SFDC Development/Apex Programming
SFDC Certifications
Job Title : Quality Control Research Associate
Duration : 6 Months (Possibility of extension)
Location : Gaithersburg, MD
Job Responsibilities::
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 biotechnology product development services. The Company focuses on providing laboratory equipment, chemicals, supplies and services used in healthcare, scientific research, safety, and education.
Position Summary:
The evaluation of quality control samples sterility testing for plated and non plated media, control of documents, setting and evaluation of class II AST products, setting up primary stock cultures, cultivation of cryogenic stock cultures and maintaining good general laboratory practices.
NOTE: This is a weekday position on a day shift and possible dayshift weekend hours as needed.
Key Responsibilities:
Review and maintain product compliance specifications, documentation control.
Gain proficiency on all technician benches.
Documentation of testing results and determination of aesthetic quality on the finished product.
Maintain consistency for training tasks in Master Control.
Maintain SOP criteria for inspection/testing.
Responsible for maintaining department equipment and ordering consumable stock supplies when necessary.
Exercise GMP compliance in the work environment.
Work well in a high volume fast-paced environment.
Work closely with the Quality Assurance department as a quality team.
Work with the continuous improvement program within the department.
Understand and exercise all safety requirements and procedures.
Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations.
Accomplish department goals.
Support all company policies.
Performs other duties as assigned.
Minimum Requirements/Qualifications:
Possess a high school diploma or equivalent.
Some laboratory experience in a biological sciences laboratory is preferred.
A minimum combined 1-2 years of experience in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience is a plus.
Some familiarity with FDA regulations for medical devices.
Possess the ability to manage many tasks and in an organized fashion.
Able to communicate effectively with a variety of departments regarding quality testing parameters.
Possess intermediate computer skills, preferably with experience in Microsoft word to include Word, Excel and PowerPoint programs. Experience working in SAP is a plus.
Listen to, and follow, written and verbal instructions.
Able to adapt and to learn new procedures and to maintain a scientific and objective approach.
Must be available to work weekend shifts when needed.
Must maintain a professional workplace attitude.
Self-motivated, highly responsible and possess a good teamwork spirit.
Excellent verbal and written skills in English.
QUESTIONS:
How long you have experience in Manufacturing?
How long you have experience as a Quality Control Technician?
Do you have working experience with GMP's/SOP's and ISO regulations?
Would you be comfortable to work on weekends?
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 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:
Using standard operating procedures (SOP) and good manufacturing practices (GMP), the Engineer/Scientist I will analyse and report external laboratory data, perform testing of filled bottle components and finished goods kits.
The Engineer/Scientist I will be responsible for all aspects of laboratory testing, such as sample receipt, data generation, product verification, data analysis and summarization, instrument operation, and all other QC lab supporting activities.
Major Responsibilities:
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 that 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 cleanups.
Participates in interdepartmental and team meetings.
Performs other responsibilities to support the needs of the department as assigned by the Supervisor.
Minimum Requirements/Qualifications:
Minimum BS/BA in Chemistry, Biochemistry, or Bioscience with 0-2 yrs Quality
Assurance/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.
Job Title: Engineer Scientist/QC
Location: Fremont, CA
Duration: 6 Months
Summary:
Job Description:
Education and Qualifications:
Title: Quality Auditing coordinator
Location: San Diego, CA
Duration: 12 months (possibility of Extension)
Responsible