Document receipt of stability samples and complete inventories. Appropriately handle documentation. Understand stability requirements protocols LIMS storage chamber conditions labeling of samples and storage positions. Provide support for project managers and laboratory staff. Compose business appropriate communication (i.e. e-mail document) for client or internal use.
Essential Duties and Responsibilities:
- Applies GMP/GLP in all areas of responsibility as appropriate
- Demonstrates and promotes the company vision Regular attendance and punctuality
- Applies quality to all areas of responsibility understands and promotes quality culture.
- Understand and update LIMS appropriately for protocol and sample activities.
- Manage inventory for incoming project samples; set up stability studies label samples and place into chambers.
- Verify sample chamber placement labeling container counts and LIMS entry
- Pull samples from chambers at appropriate intervals; perform periodic chamber inventories
- Maintain contents of stability chambers in an organized manner monitor and change charts; clean inside of chambers
- Follow all department procedures and SOPs; understand and apply GMP/GLP regulations to daily work; document data according to regulatory requirements
- Attend department meetings
- Independently evaluate and/or provide shipment paperwork package samples for shipment as needed with additional training.
- Effectively use word tone body language to share and receive information.
- Accept and implement process change to support business goals.
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
Qualifications :
Minimum Qualifications:
- High school diploma 1 year of relevant experience (minimum) or college degree in related field.
- Ability to work in the US without immediate or potential future sponsorship.
- Computer skills
- Stability experience preferred.
- Good oral and written communication skills
- Attention to detail
- Self-motivated
Additional Information :
Working schedule will be Full-Time First Shift M-F 9am-5pm. Candidates currently living within a commutable distance of Lancaster PA are encouraged to apply. No relocation assistance will be given. This position is NOT remote.
What we Offer:
- Excellent full time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
Document receipt of stability samples and complete inventories. Appropriately handle documentation. Understand stability requirements protocols LIMS storage chamber conditions labeling of samples and storage positions. Provide support for project managers and laboratory staff. Compose business appr...
Document receipt of stability samples and complete inventories. Appropriately handle documentation. Understand stability requirements protocols LIMS storage chamber conditions labeling of samples and storage positions. Provide support for project managers and laboratory staff. Compose business appropriate communication (i.e. e-mail document) for client or internal use.
Essential Duties and Responsibilities:
- Applies GMP/GLP in all areas of responsibility as appropriate
- Demonstrates and promotes the company vision Regular attendance and punctuality
- Applies quality to all areas of responsibility understands and promotes quality culture.
- Understand and update LIMS appropriately for protocol and sample activities.
- Manage inventory for incoming project samples; set up stability studies label samples and place into chambers.
- Verify sample chamber placement labeling container counts and LIMS entry
- Pull samples from chambers at appropriate intervals; perform periodic chamber inventories
- Maintain contents of stability chambers in an organized manner monitor and change charts; clean inside of chambers
- Follow all department procedures and SOPs; understand and apply GMP/GLP regulations to daily work; document data according to regulatory requirements
- Attend department meetings
- Independently evaluate and/or provide shipment paperwork package samples for shipment as needed with additional training.
- Effectively use word tone body language to share and receive information.
- Accept and implement process change to support business goals.
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
Qualifications :
Minimum Qualifications:
- High school diploma 1 year of relevant experience (minimum) or college degree in related field.
- Ability to work in the US without immediate or potential future sponsorship.
- Computer skills
- Stability experience preferred.
- Good oral and written communication skills
- Attention to detail
- Self-motivated
Additional Information :
Working schedule will be Full-Time First Shift M-F 9am-5pm. Candidates currently living within a commutable distance of Lancaster PA are encouraged to apply. No relocation assistance will be given. This position is NOT remote.
What we Offer:
- Excellent full time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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