Jobs in Qa-Quality-Control

Salesforce Admin 42
Algorithm    12-05-2019 Durham, NC, USA

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:

  • Administration of Profiles, Roles, Permission Sets & package license assignments.
  • Create and manage workflow rules, data validation, and triggers
  • Analyze data and execute data migration strategies using Sf Wizard, Apex data loader, MS Excel, workbench.

 Day to Day job Duties:(what this person will do on a daily/weekly basis)

  • Maintain and customize Sales Cloud, Service Cloud and Partner Cloud applications.
  • Working with the Team and Business on grooming user stories in Agile methodology.
  • Understand the fundamentals of iterative and incremental development.
  • Well understanding of software development processes and procedures to understand his team needs.
  • Helping with new user setups and solving access issues across the board.
  • Dealing with SSO, two-factor authentication, and certificate problems.
  • Helping end users to develop and fine-tune reports so they yield meaningful metrics.
  • Helping with post database refresh issues and follow the best practices of Salesforce.

Basic Qualifications: (what are the skills required to this job with minimum years of experience on each)

  • Minimum 5+ years of experience working as a Salesforce Admin in Sales Cloud, Service Cloud, HR, Customer Service and Marketing with Enterprise level applications
  • Minimum 3+ years of experience working with mid to large size teams with problem solving, and analytical skills needed to support enterprise high availabilitySalesforceapplications
  • Knowledge of agile methodology and frameworks like Scrum and Kanban etc.

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

QA Specialist - I 6
TekWissen LLC    12-03-2019 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 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
 
RESPONSIBILITIES: 
  • Provide on-the-floor QA oversight and support to ensure compliance to GMP throughout the area
  • Provide Quality Assurance support involving manufacturing production issues
  • Ensure that Client products are manufactured in compliance with site, regulatory and GMP guidelines Ensure timely issuance of production records and labels
  • Elevate issues affecting lot production or release to Management in a timely manner
  • Ensure approval and timely delivery of Final Product
  • Review and approve executed Manufacturing Production Records for regulatory and Client compliance
  • Compile and verify all batch-related documents into a Final Product lot disposition package
  • Perform quality review and/or investigations of manufacturing deviations, GMP and Quality System issues, non-conforming materials, and CAPA, as needed
  • Gather metric information for use in continuous improvement of areas of responsibility, as needed
  • Perform other duties as required to fulfill department and business needs
 
REQUIREMENTS:
  • Bachelor’s degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with a minimum of 2-4 years of experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility
  • Working knowledge of GMP, quality systems and regulatory requirements (21 CRF Part 11/210/211/600/610), practices/principles
  • Knowledge of relevant ICH and FDA guidance documents
  • Experience in identifying deviations and CAPA
  • General knowledge of aseptic manufacturing processes
  • Proficient in MS Word, Excel, PowerPoint and other applications
  • Strong written and verbal communication skills
  • Ability to communicate and work independently with scientific/technical personnel
 
PREFERRED REQUIREMENTS:
  • Experience with cell therapy manufacturing
  • ASQ certification(s)
  • Experience with internal and external audit
  • Experience in warehouse management
  • Experience with Health Authority Regulations and Validation practices/principles
  • Experience in working directly as QA or principal for Facilities and Engineering
  • Knowledge of IQ/OQ/PQ
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
 
Questions:
  1. How many years of QA Specialist experience do you have in biotechnology, biologics, or pharmaceutical?
  2. Years of experience in identifying deviations and CAPA?
  3. Do you have a working knowledge of GMP, quality systems and regulatory requirements?
  4. Do you have an ASQ certification?
  5. How many years of internal and external audit experience do you have?
Quality Control Research Associate 17
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.

 

Quality Control Technician 1 21
TekWissen LLC    11-26-2019 Lenexa, KS, 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 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: 

  1. How long you have experience in Manufacturing? 

  2. How long you have experience as a Quality Control Technician? 

  3. Do you have working experience with GMP's/SOP's and ISO regulations? 

  4. Would you be comfortable to work on weekends? 

Quality Control 13
TekWissen LLC    11-25-2019 Fremont Blvd, Fremont, 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 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. 

Engineer Scientist 28
Integrated Resources, Inc    11-25-2019 Fremont, CA, USA

Job Title: Engineer Scientist/QC

Location: Fremont, CA

Duration: 6 Months

 

Summary:

  • 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.

 

 

QA Specialist - I 21
TekWissen LLC    11-19-2019 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 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
 
RESPONSIBILITIES: 
  • Provide on-the-floor QA oversight and support to ensure compliance to GMP throughout the area
  • Provide Quality Assurance support involving manufacturing production issues
  • Ensure that Client products are manufactured in compliance with site, regulatory and GMP guidelines Ensure timely issuance of production records and labels
  • Elevate issues affecting lot production or release to Management in a timely manner
  • Ensure approval and timely delivery of Final Product
  • Review and approve executed Manufacturing Production Records for regulatory and Client compliance
  • Compile and verify all batch-related documents into a Final Product lot disposition package
  • Perform quality review and/or investigations of manufacturing deviations, GMP and Quality System issues, non-conforming materials, and CAPA, as needed
  • Gather metric information for use in continuous improvement of areas of responsibility, as needed
  • Perform other duties as required to fulfill department and business needs
 
REQUIREMENTS:
  • Bachelor’s degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with a minimum of 2-4 years of experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility
  • Working knowledge of GMP, quality systems and regulatory requirements (21 CRF Part 11/210/211/600/610), practices/principles
  • Knowledge of relevant ICH and FDA guidance documents
  • Experience in identifying deviations and CAPA
  • General knowledge of aseptic manufacturing processes
  • Proficient in MS Word, Excel, PowerPoint and other applications
  • Strong written and verbal communication skills
  • Ability to communicate and work independently with scientific/technical personnel
 
PREFERRED REQUIREMENTS:
  • Experience with cell therapy manufacturing
  • ASQ certification(s)
  • Experience with internal and external audit
  • Experience in warehouse management
  • Experience with Health Authority Regulations and Validation practices/principles
  • Experience in working directly as QA or principal for Facilities and Engineering
  • Knowledge of IQ/OQ/PQ
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
Quality Control Chemist - I 23
TekWissen LLC    11-19-2019 Santa Monica, CA 90404, USA
Overview: 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.
 
  • Conducts routine and non-routine analysis of raw materials samples according to standard operating procedures (SOPs). 
  • Reviews data and results of testing to ensure compliance with appropriate specifications and protocols. 
  • Troubleshoots basic instrumentation/test methods.

 
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
Quality Control Chemist - I 15
TekWissen LLC    11-19-2019 Santa Monica, CA 90404, USA
Overview: 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.
 
  • Conducts routine and non-routine analysis of raw materials samples according to standard operating procedures (SOPs). 
  • Reviews data and results of testing to ensure compliance with appropriate specifications and protocols. 
  • Troubleshoots basic instrumentation/test methods.

 
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.
Quality Auditing coordinator 22
Integrated Resources, Inc    11-18-2019 San Diego, CA, USA

Title: Quality Auditing coordinator

Location: San Diego, CA
Duration: 12 months (possibility of Extension)

Responsible

  • Documenting and analysis of metrics
  • Assisting in disposition of product in MRB
  • Quality Agreement generation and maintenance.

 

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