Process Scientist I Job at Diasorin (Stillwater)

Process Scientist I

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

Location

United States , Stillwater

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associates degree in Chemistry, Biology or Medical Technology required
Bachelor's or Master's degree preferred in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience
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, grasping complex concepts and solutions, problem-solving and analytical skills

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

What we offer

Health benefits
Retirement and financial wellbeing
Time off programs
Wellbeing support and perks
Annual incentive program eligibility

Fulltime

Process Scientist I

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

Location

United States , Stillwater

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associates degree in Chemistry, Biology or Medical Technology required or Bachelor's or Master's degree preferred in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience
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

What we offer

health benefits
retirement and financial wellbeing
time off programs
wellbeing support and perks
annual incentive program

Fulltime

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

Scientist III or Principal Scientist I - LC-MS and Analytical Support

We are looking for a Scientist III or Principal Scientist I – Liquid Chromatogra...

Location

United States , Rahway

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry or a closely rated field and 3 to 5 years of relevant experience or a Master’s degree in Chemistry or a closely rated field and 1 to 2 years of relevant experience (Scientist III)
Bachelor’s degree in a relevant field with at least 3-5 years of experience or a Master’s degree in a relevant field with at least 1-2 years of experience (Principal Scientist I)
Reversed-phase high-performance liquid chromatography (RP-HPLC)
Experience with Waters, Sciex, or Agilent LC-MS instrumentation and software
High resolution mass spectrometry
Strong communication and coordination skills

Job Responsibility

Checks instrument performance and suitability routinely, prepares mobile phases, and performs routine upkeep of open access LC-MS instruments
Maintains accurate documentation and records, data/file transfer, etc.
Communicates status of instruments to end-user
Responds to end-user repair calls for LC-MS instruments and troubleshoots/repairs simple issues such as leaks or clogs
Submits and coordinates repair tickets for more complex issues
Assist with purity analysis of investigational compounds by LC and high-resolution MS experiments
Support the installation and qualification process for open access instruments, including coordination with vendors
LC and LC-MS analysis of small molecule samples as needed

What we offer

full benefits
sick time
401K
paid holidays
paid time off

Fulltime

Assoc Scientist I-2

This is where your work makes a difference. At Baxter, we believe every person—r...

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

Job Responsibility

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

Scientist I, Quality Control (2nd Shift)

Carex is partnering with a Pharmaceutical industry partner to identify a Scienti...

Location

United States , Madison

Salary:

Not provided

Carex Consulting Group

Expiration Date

Until further notice

Requirements

M.S. in Chemistry or a related scientific field with 7+ years of relevant laboratory experience
or B.S. in Chemistry or a related scientific field with 9+ years of relevant laboratory experience
Extensive knowledge of cGMP requirements, ICH guidelines, and pharmaceutical quality control laboratory operations
Demonstrated experience with analytical method validation, method transfers, and routine testing in a regulated environment
Strong proficiency with analytical instrumentation, data acquisition systems, and laboratory software platforms
Ability to independently execute complex analytical testing and make scientifically sound decisions
Experience reviewing technical data and supporting quality investigations and corrective actions
Strong troubleshooting skills related to instrumentation, analytical methods, and laboratory processes
Excellent written and verbal communication skills
Strong organizational skills and attention to detail

Job Responsibility

Perform analytical method validation, method transfer, and routine testing of pharmaceutical raw materials, in-process samples, finished products, and stability samples
Execute laboratory testing using established analytical methods, procedures, and instrumentation
Collaborate with Analytical Development and Manufacturing teams to support validation activities and project timelines
Operate, calibrate, maintain, and troubleshoot analytical instrumentation with minimal oversight
Demonstrate expertise with analytical technologies including HPLC, GC, LC-MS, Karl Fischer, FTIR, endotoxin plate readers, Raman spectroscopy, and related systems
Analyze and interpret data, including tracking and trending stability results and identifying degradation patterns
Utilize stability tracking software for data entry, review, approval, and record management
Lead technical discussions, scientific problem-solving sessions, and laboratory investigations
Identify, troubleshoot, and resolve analytical method, instrumentation, and sample-related issues
Review analytical data generated by other QC analysts to ensure accuracy and compliance

Fulltime

Associate Scientist I

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

Knowledge of small molecules analytical projects
Organizational skills with demonstrated attention to detail
Ability to apply a logical and methodical approach to analytical and quality processes and to formulate sound recommendations
Good understanding of GMP standards in a laboratory environment
Ability to work on multiple tasks simultaneously while meeting deadlines
Strong interpersonal skills with the ability to collaborate effectively within cross-functional teams
Quality-oriented mindset
Master in Science degree (e.g. Analytical Chemistry, Organic chemistry, Biochemistry, Bio-engineering, Pharmaceutical Science)
Minimum of 2-6 years of experience in pharmaceutical industry (R&D, manufacturing…)
Demonstrated expertise in reviewing analytical chemistry data (e.g. experiments, reports)

Job Responsibility

Maintain schedules for periodic reviews of test method assays in collaboration with the management and analytical SMEs. Monitor tasks progress and identify potential planning risks
Manage change control activities related to test method assay periodic reviews and updates in accordance with project needs and agreed timelines
Contribute to R&D analytical activities by reviewing experiments within her/his area of technical expertise
Support analytical projects through effective collaboration in documentation management
Contribute to the continuous improvement of quality processes within R&D analytical 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

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Process Scientist I

Job Description

Job Responsibility

Requirements

What we offer

Looking for more opportunities?

Process Scientist I

Process Scientist I

Process Scientist I

Process Scientist I

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

Scientist III or Principal Scientist I - LC-MS and Analytical Support

Assoc Scientist I-2

Scientist I, Quality Control (2nd Shift)

Associate Scientist I

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