Process Scientist I Job at Diasorin (Stillwater)

Process Scientist I

This position is responsible for material processing, reagent formulation, techn...

Location

United States , Stillwater, Minnesota

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associates degree in Chemistry, Biology or Medical Technology required
1+ years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry
Basic understanding of immunology and immunoassay techniques
Ability to work in a regulated environment
Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
Working knowledge of MS Excel
familiarity with Google Suite
Basic understanding of statistical analysis
Advanced skills in: Math and calculations
Writing and documentation

Job Responsibility

Perform material processing and reagent for formulation bulk intermediates and components
Determine reprocessing need for calibrator, controls, and conjugates with assistance
Perform Good laboratory practices - maintain clean workspace in QC and Reagent Prep labs. Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility
Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc.
Perform in-process testing and final Quality Control for LIAISON products per established procedures using the LIAISON analyzer family
Assign calibrator values to optimize kit performance
Assign kit control ranges per established procedures
Monitor internal control supplies and manufacture new controls as needed
Perform second-checking to ensure accurate records

What we offer

comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks
may be eligible to participate in an annual incentive program

Fulltime

Scientist II/Sr. Scientist I, Analytical Research and Development

We are seeking a Scientist II/ Senior Scientist I with hands‑on experience in ph...

Location

United States , Cambridge

Salary:

130000.00 - 180000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Degree in a relevant discipline (biochemistry, biotechnology, biological sciences, bioengineering, or related fields)
Minimum PhD with 2+ years or BS/MS with 10-15 years industry experience
Must have hands-on experience on analytical method development, optimization, qualification, and testing at GMP or non-GMP environments, supporting clinical phase programs
Experience with analysis of RNAs, proteins, protein conjugates, lipids, and lipid nanoparticles (LNPs) is highly desirable
Extensive experience with at least one or several of the analytical techniques is required: HPLC (RP, IPRP, SEC, IEX), capillary gel electrophoresis, ELISA
Experience with qPCR, DNA and RNA extraction, western blotting, UV spectrophotometry, DLS, MALS, mass spectrometry, and compendial testing will be a plus
Experience with analytical CMC development, method transfer, and QC technical support is highly desirable
A good understanding of ICH Q2 and Q14, with working knowledge on analytical Quality by Design concept
Familiarity with data analysis software such as Openlab, Chromeleon, and statistical software such as JMP
Team player with excellent oral and written communication skills

Job Responsibility

Lead early through late phase method development, optimization, and transfer for lot release, stability, and characterization of drug substances, critical materials, and drug products
Establish technical leadership as subject matter expert in multiple analytical techniques during method development and transfer and provide technical troubleshooting support when needed
Work with cross-functional groups including Research & Development, Quality Control, and Process Development teams to participate in various aspects of method development, transfer, characterization, comparability, and investigation
Coordinate routine sample testing including requests from Research and Development groups and Process Development teams
Author and review SOPs, technical reports, and assist in the preparation of CMC regulatory submissions
Analyze, track, and trend data to monitor analytical assays and ensure consistency in assay performance
Maintaining detailed documentation of experiments in ELN system
Adapting to a fast-paced, dynamic research environment
Mentor and train junior scientists
Living Beam Therapeutics core values

Fulltime

Associate Scientist, Process Development (Process Validation & Business Strategy)

In this vital role you will be a part of the Process Development Drug Substance ...

Location

United States , Holly Springs

Salary:

97377.00 - 118653.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 3 years of Process Development or Scientific experience
Master’s degree and 1 years of Process Development or Scientific experience
2 – 4 years of experience in a Biotech/Pharma Process Development, MFG, QC, or laboratory role
Knowledge in broad aspects of biologics processing, for example cell culture, purification, analytical methods, or product quality attributes
Familiarity in operational aspects of process development lab or commercial biopharma manufacturing
Experienced with software such as Holistic Lab Execution Environment (HLEE), Tableau, MS PowerBI, spotfire, and/or databricks
Able to apply digital tool skills to solve business process issues and evaluate opportunities for process improvements
Excellent written and verbal communication
Be a self-starter with the ability to take on several projects at one time.

Job Responsibility

Lead and develop the Process Development safety, training, and compliance monitoring operation
Holistic Lab Execution Environment (HLEE) champion for the process development lab
Develop digital tools to improve business process efficiencies and identify bottlenecks within the process development operation
Develop digital tools to support process validation and process monitoring activities
Support and develop the Amgen North Carolina (ANC) PD DST knowledge management ecosystem, alignment of ANC PD business process to network practice, and optimizing the ANC PD business process
Provide process floor or lab support as required.

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Fulltime

New

Regional Process Scientist

We provide water to 1.4 million customers and treat the sewage of 2.9 million cu...

Location

United Kingdom , Bath

Salary:

45000.00 GBP / Year

Wessex Water

Expiration Date

June 30, 2026

Requirements

a degree (or equivalent experience) in Science or an environmental subject
IT literacy
strong knowledge of wastewater treatment processes
an understanding of the wastewater regulator environment
the ability to interpret and analyse scientific data
experience presenting technical data to senior leaders
a full driving licence

Job Responsibility

leading root cause analysis meetings following incidents
identifying solutions and areas for improvement on small and large scales
designing and implementing initiatives to improve performance
monitoring and reporting on environmental performance and improvements
providing information for regulatory requirements
analysing scientific data to provide actionable insights
collaborating with people across the business to ensure consistency and promote cross-team learning
delivering basic training on root cause analysis processes

What we offer

A combined pension contribution of up to 20%
Career progression and professional development opportunities
25 days' holiday rising to 28 with length of service
The opportunity to buy up to 10 days' holiday and sell up to five every year
A healthcare package that allows you to claim back healthcare costs
Life assurance of up to eight times your salary
A new electric car in exchange for part of your gross salary
Cashback and discounts from more than 3,000 retailers
One paid volunteering day each year
Enhanced family leave and pay arrangements

Fulltime

Qc Associate Scientist I

We are seeking a proactive and detail-oriented QC Associate Scientist to join ou...

Location

United Kingdom , Basingstoke

Salary:

14.00 - 14.14 GBP / Hour

Randstad

Expiration Date

August 24, 2026

Requirements

Qualified to a Level 6 equivalent (Degree) in Microbiology or a related biological science subject
Practical experience working within a microbiology laboratory environment
Proficiency in basic laboratory techniques (streaking, pouring plates, pipetting) and good numerical skills
Ability to follow strict SOPs and methods precisely, strong organization skills, a proactive attitude, and a commitment to health and safety standards

Job Responsibility

Carry out microbiological Quality Control testing in accordance with standard test specifications and methods
Perform core laboratory tasks including media preparation, plating out, streaking, swabbing, pipetting, and utilizing autoclaves
Record test results accurately within company management software (SAP) and maintain precise training records
Complete Out of Specification (OOS) reports and assist with laboratory investigations
Maintain laboratory standards through equipment checks, cleaning, waste management, and restocking consumables
Participate in daily team meetings and contribute to continuous improvement and lean processes

Fulltime

Assoc Scientist I-2

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Serve as a verifier of biocompatibility information documented in protocols, reports, toxicology risk assessments, BEP/BER or materials in the material database
Maintain the Material Database in Team Center Unified (TcU) and serve as the system administrator Validating software updates made to the material database
Generation of purchase orders for work performed at the external laboratories
Employ appropriate techniques/methods to execute routine assignments successfully and independently within negotiated deadlines
Maintain knowledge of relevant regulatory and biocompatibility requirements in accordance with ISO 10993 series of standards for device registration and global compendia for drug registrations
Recommend appropriate designs, techniques, and processes for a specified sequence of tasks where needed
Have a working knowledge and understanding of Good Laboratory Practice (GLP) / Good Manufacturing Practice (GMP) and related regulations and guidance
Receiving and handling samples for testing, coordinating sample shipments to external laboratories

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Clinical Lab Scientist I

This position is accountable for performing clinical laboratory testing, followi...

Location

United States , San Juan Capistrano

Salary:

40.00 - 56.44 USD / Hour

Quest Diagnostics

Expiration Date

Until further notice

Requirements

Zero to three year’s direct experience in a laboratory setting
Ability to perform repetitive tasks
Frequent simple grasping, reaching and fine manipulation
Ability to sit and/or stand for long periods
Have good eye and hand coordination
Testing for color blindness will be required upon hiring or transfer into technical functions requiring detection of, or rating of intensity of colors (e.g., Fluorescent microscopy reading)
Proficiency in Microsoft Office Application (Word, Excel, Outlook)
Bachelor’s Degree Medical technology or other life or physical sciences from an accredited college or university
Current State Clinical Laboratory Scientist license if necessary (e.g. California)

Job Responsibility

Independently performs moderate to highly complex clinical tests following the required procedures and policies
Performs newly introduced tests to the laboratory that require defined skills
Prepares and oversees the preparation of reagents or media as well as stock solutions, standards, and controls
Tests new reagents or controls and evaluates their usefulness based on standard criteria
Determines the acceptability of specimens for testing according to established criteria in testing procedures
Determines calculated results utilizing testing data by means of manual or computerized procedures
Accurately enters results of testing
Checks the computer review reports to monitor accurate reporting of laboratory results
Adheres to analytical schedules to maintain turnaround times of results
Evaluates the acceptability of routine and complex analyses prior to releasing patient reports

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 MyDay off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Scientist I

The Scientist I – Chemical, Industrial, Materials Science, Materials Engineering...

Location

United States of America , Pensacola

Salary:

Not provided

Danaher Corporation

Expiration Date

Until further notice

Requirements

A bachelor’s degree in chemical engineering, biomedical engineering, mechanical engineering, etc.
Detailed oriented and able to multitask in a fast-paced environment
Someone with good understanding of process development and scaleup
Someone with additional lab work experience in the form of internships, co-ops, or similar
A reliable team player that is also able to work alone efficiently when needed

Job Responsibility

Focus on process optimization, process scaleup, data analysis and equipment upgrades of new membrane technologies for current and future applications
Collaboration with scientists on new membrane technologies to develop proof-of-concept, process optimization and scale up
Prototypes manufacturing and interaction with customers during testing
Maintain accurate, organized data and detailed description of experiments in both electronic and physical notebooks, being capable of clearly communicating data and observations orally and through presentations

What we offer

paid time off
medical/dental/vision insurance
401(k)

Fulltime

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Process Scientist I

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