Job Description

Training Specialist - QC/Analytical
Job Number: 21-15253
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Training Specialist - QC/Analytical for our client in Summit, NJ.
 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!

Position Overview:
  • Will work both independently and with the team to perform QC analytical testing training and QC laboratory maintenance functions, where necessary.

Responsibilities:
  • Carry out responsibilities in accordance with the organizations policies, procedures, and state, federal and local laws.
  • Ensure compliance with current Good Manufacturing Procedures (cGMP), USP, EU and other global regulatory requirements at all times.
  • Follow directions properly, work cooperatively as an individual contributor and as a team member.
  • Communicate effectively with QC peers, cross-functional peers and management.
  • Performs general laboratory cleaning/wipe-down.
  • Perform routine maintenance of lab equipments
  • Under the guidance of management, support special project work.
  • Maintain lab inventory and order lab supplies and materials.
  • Support continuous improvement projects related to QC
  • Assist with investigations & CAPAs associated with QC-analytical testing.
  • Support data trending and tracking of results.
  • Perform all other duties as assigned.
 
Qualifications:
  • Requires Bachelors degree in Biology or Chemistry related discipline and minimum 3 years of experience working in a regulated quality control (QC) laboratory. QC- Analytical lab training experience & Masters Degree strongly preferred. An equivalent combination of experience/education
  • Have a good understanding of USP, EP, JP, and FDA testing requirements.
  • Experiences with some of following QC-Analytical methods: Flow Cytometry, ELISA, PCR, Cell Count, Vector Copy Number Determination, Mycoplasma PCR.
  • Training experience is preferred
  • Experiences on HPLC, UPLC, or GC is plus.
 
Required Skills:
  • Advanced hands-on experience with various analytical techniques primarily flow cytometry or PCR or ELISA and scientific knowledge in the characterization and transfer of pharmaceutical products.
  • Advanced ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
  • Advanced technical writing skills.
  • Advanced problem-solving ability/mentality, technically adept and logical.
  • Ability to represent the interests of the group on cross-functional teams.
  • Ability to work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects.
  • Ability to work with management locally and globally.
  • Advanced ability to communicate effectively with peers, department management and cross functional peers.
 
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
 
If interested, you may contact:
Chris Imbien
Chris.imbien@eclaro.com
8428729257
 
Equal Opportunity Employer:
 Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.                                                     

Application Instructions

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