Quality Control (LIMS) Pharmaceutical Manufacturing
SRG, the leader in the Life Sciences human capital industry, is looking for a full-time, contract LIMS Quality Control consultant to join our client's pharmaceutical manufacturing team in upstate Vermont.
Must Haves:
- Experience with instrument integration into a software package
- LIMS/Master Data integration experience
- Quality Control
- Balanced integration into LIMS, paper-based to paperless
- Knowledge of lab processes
Responsibilities:
- Helping with automation project impacting LIMS system
- Transition from paper-based to all paperless in terms of manufacturing laboratory
- Integrating those instruments in LIMS to get to paperless
- Balance integration into LIMS
- Work with site/global teams to document site requirements and create new procedures
**Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.
Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.
If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.
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