Central Services Technician

Harmans, MD

Posted: 08/22/2023 Division: Life Sciences Job Number: JN -082023-17422

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.

  • Location: Harmans, MD
  • Industry: Central Services Technician
  • Hours: 7am-7pm (2-2-3 rotating schedule) (must be able to work 7pm-7am for training)
  • Salary: Up to $22.57 hour paid weekly with benefits options
  • Employment Type: 3 month Contract to hire role

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. Isn t this the type of company you want to work for?

Description: The Central Services Technician I performs and documents cGMP activities related to Central Services production and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed

Job Duties:

  • Performs Processing Steps and/or Manufacturing Support activities, monitoring process against the batch record.
  • Documents/Records cGMP data and information for processing steps and/or equipment activities, following standard operating procedures. Key documentation includes batch records and equipment logbooks.
  • Understands basic cGMP requirements and follows those requirements, including requirements for good documentation practices.
  • Completes /reviews validation protocols, deviation reports, change controls in accordance with cGMP s
  • Performs the weighing, dispensing of raw materials for media and buffers
  • Performs the preparation of small and large volume media and buffer solutions, filtration and transfer of product.
  • Operates bench top equipment including pH, conductivity, osmo meters, pumps, tubing welders, filter integrity testers etc.
  • Dispensing, labeling, transfer/staging of raw materials and parts
  • Assembly/disassembly, cleaning and sterilization of components, parts and equipment
  • Maintaining equipment, area and cleaning logbooks
  • Cleaning sanitizing production rooms and equipment
  • Stocking production and cleaning supplies
  • May author/ review/improve SOP s, batch records, protocols and technical reports
  • Actively participates in training activities, managing their individual training plan.
  • Proficient and knowledgeable in the operation and basic troubleshooting of at least one manufacturing area.

Skills Needed:

  • High School Diploma with a minimum of 2-4 years GMP Manufacturing experience, OR
  • Certificate and/or Associate s Degree in a scientific, engineering or biotechnology discipline with a minimum of 0-2 years related experience; coursework with biotechnology focus highly desirable, OR
  • Bachelor s Degree (BS/BA) from an accredited college or university with an emphasis in a scientific or engineering discipline and a minimum of 0-1 years relevant experience
  • Basic knowledge of current Good Manufacturing Practices (cGMP s). Working knowledge of all relevant safety procedures within the company. General understanding of most areas in Manufacturing and supporting functional groups.
  • Familiar with or experience with cGMP Biotech or Pharmaceutical operations:
  • Must be team-oriented (proactively builds healthy working relationships between peers, their department and other groups).
  • Able to fluently communicate in English. Exhibits excellent written and oral communication skills.
  • Possesses a basic knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management.




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