drjobs
Lab Analyst III IV or V
drjobs
Lab Analyst III IV o....
TekWissen LLC
drjobs Lab Analyst III IV or V العربية

Lab Analyst III IV or V

Employer Active

1 Vacancy
The job posting is outdated and position may be filled
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs

Job Location

drjobs

Willow - USA

Monthly Salary

drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2572448
Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Our client is an is a global animal health company dedicated to supporting customers and their businesses in ever better ways. Building on more than 65 years of experience it deliver quality medicines vaccines and diagnostic products complemented by biodevices genetic tests and precision livestock farming.
Job Title: Lab Analyst III IV or V
Work Location: 1 Duggar Drive Willow Island WV USA
Duration:6 Months Possible Extension
Job Type: Contract
Work Type: Onsite
Client: Zoetis
Shift: 40 hours MondayFriday (8am 5pm)
Pay Rate: $26.00/Hour
Job Description:
  • The Laboratory Analyst position supports the Medicated Feed Additives (MFA) business of client in Willow Island WV.
  • The Quality Control laboratory provides testing and release support for the Willow Island manufacturing site.
  • The preferred candidate will meet the criteria for an Analyst III IV or V level as described below.
POSITION RESPONSIBILITIES:
  • Receives and prepares samples for analytical testing and initiation of stability studies.
  • Performs physical testing of routine and nonroutine samples with little supervision including but not limited to raw materials in process testing API & finished good release and stability testing.
  • Supports the site quality safety and production needs and goals compliantly.
  • Works within crossfunctional teams.
  • Coordinates own work assisting the lab to complete priority projects.
  • Completes all activities following site cGMP Safety requirements and client Standards.
  • Conducts laboratory activities related to experiments studies and projects in support of production laboratory or other client groups
  • Understands and follows cGMP regulations
  • Data maintenance and record keeping are in accord with GMP and SOP
  • Participates in projects and follows through to completion.
  • Supports laboratory operations using technical ability to run routine samples independently.
  • Recognizes abnormal results and/or instrument problems and reports them to supervision providing input to cause and possible solutions.
  • Performs routine tests and experiments following compendial or standard procedures
  • Has an understanding and has applied skills related to Lean & 5S.
  • Sets up adjusts and operates laboratory basic equipment such as balances pH meter sieves ovens and has an understanding and has used advanced laboratory equipment such as Viscosity Karl Fischer UV/VIS HPLC GC.
  • Maintains and follows Standard Operating Procedures dealing with their work area and can apply knowledge to assist in other work areas.
  • Generation of protocols and execution of projects with little oversight. May lead a project and be responsible for completion.
  • May assist with the writing and revising of procedures.
  • May be assigned to projects dealing with special samples needing method modifications with close supervision.
  • Records tests results on standardized forms and prepares reports describing procedures used.
  • Prepares charts and graphs to assist in evaluation and interpretation of data.
  • Completes investigations into aberrant data and generation of summary reports for their own work can apply problem solving techniques in a team environment.
  • Considered a Subject Matter Expert in Procedures for their area providing training in and out of their department.
  • Maintains a safe and clean working area and assists others in same.
  • Will work with Analysts Scientists and Management staff on a routine basis for the receipt and preparation of QC Test Samples and Stability study samples.
  • Follows good documentation practices.
  • Adheres to the client Core Beliefs demonstrating exemplary behaviours.
  • Identifying EHS hazards and propose solutions to improve lab/safety compliance.
EDUCATION AND EXPERIENCE:
ANALYST III
  • High School degree or equivalent with approximately 10 years lab experience preferably in an FDA regulated environment; or 2year degree with approximately 3 years experience or B.S. degree in a related scientific field with approximately 1.5 years of experience.
ANALYST IV
  • High School degree or equivalent with approximately 15 years lab experience preferably in an FDA regulated environment; or 2year degree with approximately 5 years experience or B.S. degree in a related scientific field with approximately 3 years of experience.
ANALYST V
  • High School degree or equivalent with approximately 20 years lab experience preferably in an FDA regulated environment; or 2year degree with approximately 10 years experience or B.S. degree in a related scientific field with approximately 5 years of experience.
TECHNICAL SKILLS REQUIREMENTS:
  • Excellent attention to detail.
  • Ability to use and perform HPLC UV GC and other instrumental techniques.
  • Ability to generate protocols and summarize data.
  • Ability to communicate within and outside immediate department. May contact vendors and/or external customers for administrative and technical information.
  • Ability to work weekends and off shifts as needed.
  • Computer literate with the following applications: MS Excel Word
  • Ability to utilize application software such as: Empower Trackwise SAP.
  • Familiarity with Lean concepts and 5S
PHYSICAL POSITION REQUIREMENTS:
  • The work environment characteristics described here are representative of those a colleague encounters while performing the essential functions of this job.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • While performing the duties of this job the colleague is regularly exposed to laboratory and office settings and a manufacturing environment.
  • The colleague will be required to utilize certain Personal Protective Equipment including but not limited to hard hats safety (steeltoed) shoes eye protection gloves and protective clothing.
  • The colleague must be able to access all areas of the plant.
TekWissen Group is an equal opportunity employer supporting workforce diversity.

Employment Type

Full Time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.