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You will be updated with latest job alerts via emailThe Opportunity:
In this role you will report to the Supervisor of Site Services and will work closely with the Avantors Lab and Production Services team of over 1500 on and offsite expert personnel and our customers to perform customized missionbased lab work and research protocols that help return time back to science.
Location:Waltham MA 02401
Shift:Mon Fri 7:00 am 3:30 pm
Wage Range: $28 30 per hour
Benefits:
Health and Wellness: Medical Dental Vision and Wellness programs (eligible for medical coverage on day 1)
Time Off: Paid Time Off (PTO) and Company paid holidays
Financial Well Being: Spending Accounts: Flexible Spending Account (FSA) Health Savings Accounts (HSA) commuter benefits 401(k) tuition assistance employee stock purchase plan discount
Added Protection Coverage: To include critical illness hospital indemnity accident legal identity theft protection pet auto and home insurance
Recognition: Celebrate your peers and earn points to redeem on gifts and products.
What were looking for:
High school diploma or GED required; Bachelor or Associate degree preferred.
12 years experience in a laboratory setting and understanding of laboratory equipment.
Basic computer skills including Microsoft Office with proficiency in Word and Excel.
Valid Drivers License and transportation.
Requires knowledge in using various instruments to prepare for and perform tests.
Must be able to lift up to 25lbs minimum.
How you will thrive and create an impact:
Avantors Lab and Production Services team is a crucial part of the Avantor Services group serving over 500 customers in biopharma pharmaceutical educational industrial and hightech industries with customizable flexible solutions and endtoend laboratory operations support.
In this role you will:
Complete routine laboratory procedures such as but not limited to preparation of solvents buffers resins reagent solutions media prep mixing of chemicals etc.
Prepare samples for analysis including blanks and standards data entry of sample log and preparation of sample submission tables.
Report timely and accurate test results according to laboratory policies and procedures
Perform routine maintenance of lab instruments and troubleshooting.
Perform small scale purification postprocessing including filling racks combining fractions dry down weighing checking fractions and obtaining final LCMS.
Store chemicals properly dispose of chemical waste adhere to safety procedures and participate in safety programs.
Manage inventory maintain process and order laboratory supplies including glassware and chemicals for biotech/pharmaceutical processes.
Update template logbook.
Maintain files track orders and process shipping requests.
Track and document chemical usage and inventory.
Glass wash and restocking chemical repacking cylinder delivery and pickup managing dry ice and liquid nitrogen dispensing and waste disposal.
Maintain clean room to prevent contamination and integrity of production.
Operate laboratory equipment and instruments.
Calibrate balances and pH meters.
Clean and prepare dissolution baths and sonicators.
Conduct hardness tests appearance tests Karl Fischer tests and disintegration tests.
Label samples and set up trays for studies.
Run inventory and label reference standards.
Inspect laboratory safety stations.
Complete basic routine laboratory procedures such as but not limited to preparation of solvents buffers resins reagent solutions media prep mixing of chemicals etc.
Track and document chemical usage and inventory.
Aliquot preparation for stocking in labs
Clean Bio Safety Cabinets monthly/quarterly
Track FBS usage and report to the proper scientist. This should include a graph to plot current use rate vs historical data for ordering purposes
Maintain a log for QC procedure for created buffers
Order consumables tools and instruments needed for the role in Coupa
Work on safety and process improvements and communicate those with the Team Lead
Cross train on Chemistry TLS team and work to coordinate that all daily responsibilities are completed. This includes daily help in reagent management
Review and change SOPs as needed. Help other team members with SOP review
Help train LRCs on what to look for with buffers and media and ensure handoffs and coordination are as efficient as possible
Other duties as assigned
Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.
Why Avantor
Dare to go further in your career. Join our global team of 14000 associates whose passion for discovery and determination to overcome challenges relentlessly advances lifechanging science.
The work we do changes peoples lives for the better. It brings new patient treatments and therapies to market giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his moms voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents learn new skills and grow your career at Avantor.
We are committed to helping you on this journey through our diverse equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!
EEO Statement:
We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex gender identity sexual orientation race color religious creed national origin physical or mental disability protected Veteran status or any other characteristic protected by federal state/province or local law.
If you need a reasonable accommodation for any part of the employment process please contact us by email at and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a casebycase basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
For more information about equal employment opportunity protections please view the Know Your Rights poster.
3rd Party NonSolicitation Policy:
By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor or by failing to comply with the Avantor recruitment process you forfeit any fee on the submitted candidates regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.
Required Experience:
Senior IC
Full-Time