Associate Scientist, Process Sciences Job at Proclinical (Cambridge)

Associate Scientist, Process Sciences

Drive innovation at the bench by helping shape next‑generation siRNA therapeutic...

Location

United States , Cambridge

Salary:

34.00 - 44.00 USD / Hour

Proclinical

Expiration Date

Until further notice

Requirements

BS in Chemistry, Chemical Engineering, Biochemistry, or a related scientific discipline
0-2 years of laboratory experience (academic, co-op, internship, or industrial experience acceptable)
Oligonucleotide experience required
Experience with Bioconjugation, antibodies, and peptides highly preferred
Familiarity with analytical techniques such as pH, conductivity, HPLC, or LC-MS is preferred
Strong attention to detail and commitment to high-quality laboratory documentation
Willingness to learn regulated laboratory practices and manufacturing workflows
Ability to work collaboratively, follow instructions, and manage time effectively
Microsoft Office Suite experience

Job Responsibility

Support process development, optimization, and scale-up of bioconjugation processes
Support oligonucleotide synthesis method development, optimization and scale-up
Execute laboratory-scale processes to support research and in-house material needs
Perform routine in-process analytical tests (e.g., pH, conductivity, UV, basic chromatography)
Assist in process development for novel chemistries
Operate laboratory and analytical equipment after appropriate training
Accurately document experimental work following good documentation practices (GDP)
Collaborate with cross-functional teams including Process Development, Analytical Sciences, and Manufacturing
Maintain a safe, organized, and compliant laboratory workspace

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

Associate Scientist Foods Product Development

As a member of the Condiments R&D team, you will support the R&D activities requ...

Location

United States , Englewood Cliffs

Salary:

59300.00 - 88900.00 USD / Year

Unilever

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Food Science, Food Engineering, Chemistry, Chemical Engineering, or a related field
1+ years of experience in food product development, R&D, or a similar technical role (internships or traineeships are highly valued)
Basic knowledge of food formulation, ingredients functionality, and processing techniques
Hands-on experience with laboratory testing, prototype development, or pilot plant work
Familiarity with food safety, quality standards, and regulatory requirements (labeling knowledge is a plus)
Exposure to cross-functional teamwork and ability to manage multiple priorities in a fast-paced environment
Strong analytical and problem-solving skills, with a structured approach to experimentation and data interpretation

Job Responsibility

Execute agreed R&D activities to deliver the brand’s program, ranging from innovation, product superiority and margin enhancement
Works as a member of a cross-functional project team to deliver projects on time in full
Independently design products against simple product briefs, design/execute test protocols for the various technical aspects of projects as required (e.g., prototype development and scale-up, shelf-life testing, analytical testing, etc.)
Lead the process of specification/label creation in SAP PLM from the request to the approved status
Actively participate and/or represent R&D in cross functional meetings
Assess feasibility of new ideas and troubleshoot activities where formulation knowledge is essential
Support technical investigations using root-cause analysis and problem-solving techniques as required for existing and new products
Develop and maintain effective working relationships with R&D, Supply Chain and Marketing teams, customers, suppliers, and key stakeholders

What we offer

Health insurance (including prescription drug, dental, and vision coverage)
Retirement savings benefits
Life insurance and disability benefits
Parental leave
Sick leave
Paid vacation and holidays
Access to numerous voluntary benefits
Bonus eligible
Long-Term Incentive (LTI) eligible

Fulltime

Associate Scientist II, R&D, Complex Product Development

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

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Master's in science with 8 to 12 years of Experience
Good experience in the execution of analytical method development, validation and technology transfer and routine analysis for peptides and iron colloidal drug products for regulatory submission
Competency with method relevant to iron DS/DP analysis, including particle size distribution by gel filtration chromatography, light scattering/diffraction/obscuration methods, assay of various iron forms, e.g. ferrous, ferric, labile iron, chelation assays, reduction potential and kinetics, etc, is strongly desired
Basic Knowledge and execution of Chemical Analysis using techniques relevant to complex injectables
Knowledge of pharmacopoeia, ICH Guidelines
Execution of Operational and Calibration of Instrument on periodic basis
Trouble shooting of various problems obtain during the during analysis
Knowledge of Transfer of Technology
Knowledge of Good Laboratory Practice and Good Documentation Practices
Communication skills

Job Responsibility

To plan and perform sample analysis (analytical method development, validation, technology transfer, etc) activity following GxP & GDP practices for regulatory submissions for complex injectables like peptides, iron formulations, etc
Assist in regulatory query responses for Complex Products
To perform testing of Complex Injectable samples, including, API, development, validation, stability, bulk hold, RLD, PDR and any other samples as required, according to appropriate method of analysis
To be competent in analytical problem-solving, focus on innovation, process improvement and operational excellence
To keep track of all activities related to product analysis, ensure completion in the stipulated time, and inform the Sub-department manager if any deviation or issues observed
Preparation and review of analytical reports, SOPs and MOAs by referring to GQP & current pharmacopoeia as per requirement
To carry out all testing and data recording according to the approved SOPs following GDP & ALCOA++ principles and current pharmacopoeia
To use appropriate reference and working standards for analysis and maintain their records
To complete all training as per the quality matrix targets
To perform or review the calibration records of instruments as per approved SOPs

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

New

Process Scientist - Critical Raw Materials

The Critical Raw Materials Scientist is responsible for performing and supportin...

Location

United States , Stillwater

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associate's Degree in Chemistry, Biochemistry, Biology or related science field required
Bachelor's Degree in Chemistry, Biochemistry, Biology or related science field preferred
1+ Years Experience in a quality control or laboratory environment preferred
Experience with SAP or similar ERP systems preferred
Effective communication and teamwork skills
Familiarity with laboratory instruments and data analysis tools
Strong attention to detail and ability to follow SOPs and regulatory guidelines

Job Responsibility

Execute functional qualification and shelf life extension testing of critical raw materials used in the production of LIAISON assays
Data analysis per written procedures and SOPs
Follow regulatory requirements - follow document instructions and maintain reasonable documentation error rates
Perform material processing and reagent for formulation bulk intermediates and components
Determine reprocessing need for calibrator, controls, and conjugates with assistance
Enter batch characteristics of LIAISON critical raw materials within the SAP inventory management system
Second check functional qualification, manufacturing, and equations related to raw material qualification, production, shelf life extension, etc
Perform Good laboratory practices - maintain clean workspace in CRM and QC labs
Contribute to CRM group 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

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
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

Associate Scientist

Amgen is seeking a hands-on dynamic Associate Scientist / Histology Technician t...

Location

United States , South San Francisco

Salary:

97574.05 - 132011.95 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Associate Degree or equivalent in Biological Science program with at least 3 years of histology laboratory experience.
HT (ASCP) or HLT (ASCP) preferred.

Job Responsibility

Perform workflows for histology preparation of specimens, including all documentation in required laboratory information systems and databases, as well as team communications.
Perform basic and advanced histology procedures (fixation and processing of tissues, embedding, microtomy, H&E staining, special stains, coverslipping, slide scanning, slide QC).
Review work to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, and procedures.
Ensure equipment is functional and maintained in good working order, and that lab safety protocols are adhered to.
Perform all other related duties as assigned.

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible.

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

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Associate Scientist, Process Sciences

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