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Central Services Technician

Harmans, MD

Posted: 12/10/2020 Industry: Manufacturing Technician Job Number: JN -122020-12283

Job Description

Central Services Technician

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: Central Services Technician
  • Location: Harmans, MD
  • Industry: Pharmaceutical
  • Hours: 2nd Shift - Hours: 2:30pm 11:00pm
  • Salary: $22.00hr (Paid Weekly - Benefits Available)
  • Employment Type: 12 month Contract
Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Job Scope:

This role is responsible for supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk products from microbial and cell culture systems for Phase I/II GMP manufacturing.
Lifting up to 40 lbs., unassisted may be required at times.
Shift work and/or weekend work may be required at times.

Knowledge/Skills Requirements:
May act as lead in the Central Services GMP Manufacturing operations.
Leverages knowledge and application of the theories and principles utilized to solve operational, as well as routine tasks in the Buffer Preparation and Technical Services areas.
Perform buffer preparations, in-process sampling without guidance.
Conducts changeover and activation procedures for clean room suites and equipment.
Submits in-process and cleaning samples to QC with required documentation.
Completes Standard Manufacturing Procedures under cGMP, and documents in detail using SOPs or the processes and manufacturing steps.
Generates operational protocol(s), internal or external documents (SOPs, SMPs), deviations and summary reports.
Working closely with various departments and offers assistance as needed.
Interacts with clients during manufacturing and audits.
May lead in conducting the GMP and Safety training of manufacturing staff.
Other duties as assigned.

SKILLS & TECHNICAL EXPERTISE:
Experience and a thorough understanding in coordination of manufacturing activities with other departments (QA, QC) to maintain internal and project schedules.
Excellent knowledge of cGMPs and computer-assisted manufacturing and production equipment.
Clean room and BL2 experience with aseptic technique training.
Ability to produce results in a fast-paced environment, under minimal supervision while leading junior staff.
Able to work in a team setting and independently under minimum supervision.
Creative individual with excellent trouble shooting skills.

Qualifications:
B.S. in a Life Sciences discipline and 4+ years of relevant experience OR
M.S. in a Life Sciences discipline and 2+ years of relevant experience
Experience within the biologic, pharmaceutical or medical device industry performing direct hands-on work with at least one of the following: aseptic formulation/filling machine operation/changeover, and operation of packaging/inspection equipment
Outstanding knowledge, and ability to apply scientific principles utilized to solve operational, as well as routine production tasks
Excellent knowledge of Good Manufacturing Practices (GMPs)

EOE/ADA


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