Manufacturing Associate

TekWissen LLC

Portsmouth, NH

JOB DETAILS
SALARY
$20–$26
SKILLS
Administrative Skills, Agriculture, Asepsis, Biology, Biotech and Pharmaceutical, Cleaning Equipment, Communication Skills, Current Good Manufacturing Practice (cGMP), Customer Support/Service, Disease, Diversity, Documentation, Equipment Maintenance/Repair, Gene Therapy, Genetics, Manufacturing, Material Science, Medical Products, Nutrition, Personal Care, Presentation/Verbal Skills, Standard Operating Procedures (SOP), Workforce Management, Writing Skills
LOCATION
Portsmouth, NH
POSTED
1 day ago
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.
Job Title: Biotechnologist Associate / Manufacturing Associate
Location: Portsmouth, NH, 03801
Duration: 12 Months
Job Type: Contract
Work Type: Onsite
Shift: NightShift from 07:00 PM to 07:00 AM (12 hours) - Rotating Shift

Responsibilities
  • The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.
  • They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
  • Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
  • Attain qualification for all assigned tasks and maintain individual training plan.
  • Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
  • Maintain facility and equipment through routine cleaning and sanitization, support 6S programs.
  • Must be willing to gown and work in a "clean room" environment.
  • Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects.
  • Perform other duties as assigned.
Required Skills & Qualifications
  • High School Diploma or equivalent experience minimum with an AS/BS preferred
  • Preferred area of study: Science related field, degrees in Genetics are relevant.
  • Prior work experience in a cleanroom, laboratory, or another sterile setting is preferred.
  • Prior experience with Aseptic Techniques and gowning procedures is preferred.
  • Working experience in manufacturing; cGMP setting preferred.
  • The ideal candidate will have experience within the Cell and Gene Therapy field.
  • Able to follow documentation procedures for day-to-day tasks in a regulated industry
  • Proven logic and decision-making abilities, critical thinking skills.
  • Strong written and verbal communication skills.
TekWissen Group is an equal opportunity employer supporting workforce diversity.

About the Company

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TekWissen LLC

WE THE TEKWISSEN PEOPLE

TekWissen offers you a broader portfolio of services, industry-leading solutions, and the meaningful innovations that give you greater flexibility and speed to respond to market dynamics, reduced costs and risk to improve enterprise performance, and increased productivity to enable growth.

To keep pace with global market demands, TekWissen keeps its finger on the pulse of change. Our organized approach to guiding a project from its inception to closure. Managing projects is becoming more and more important as we enter the digital era. To cope with the pace that this transition demands, a method is required to manage projects so they can yield quality work, while incorporating efficient use of time and resources.

Project involves identifying which quality standards are relevant to the project and determining how to satisfy them.

It is important to perform quality planning during the Planning Process and should be done alongside the other project planning processes because changes in the quality will likely require changes in the other planning processes, or the desired product quality may require a detailed risk analysis of an identified problem. It is important to remember that quality should be planned, designed, then built in, not added on after the fact.

Capabilities and accomplishments in one TekWissen business enhance the opportunity for success in the others. Put simply, TekWissen's unique combination of attributes promotes success.



COMPANY SIZE
100 to 499 employees
INDUSTRY
Computer/IT Services
FOUNDED
2009
WEBSITE
http://www.tekwissen.com/