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

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

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

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

Scientist associate r&d

As an associate scientist, you will be part of a driven team within pharmaceutic...

Location

Belgium , Strombeek-Bever

Salary:

Not provided

Randstad

Expiration Date

August 26, 2026

Requirements

You hold a master's degree in chemistry, pharmaceutical sciences, biochemistry (or a related scientific field), or a bachelor's degree with relevant experience
You demonstrate strong theoretical knowledge and hands-on expertise in liquid chromatography, IC, and/or GC
You are familiar with chromatography data systems such as Empower or OpenLab
You maintain high quality standards for your work, take accountability for your results, and adapt quickly to changing priorities
You work well independently and thrive as a positive, collaborative team player
You are proficient in English, both spoken and written

Job Responsibility

Perform precise analyses for the characterization of reference standards, focusing heavily on liquid chromatography, ion chromatography, and gas chromatography
Develop fit-for-purpose analytical methods that meet strict reporting thresholds for accurate purity determination
Support product and process characterization, method validation, and stability studies using advanced LC techniques
Ensure full compliance with relevant regulatory guidelines, specifications, GMP standards, and safety regulations
Scientifically evaluate and interpret generated analytical results to guarantee the highest quality standards

Fulltime

Scientist, Process Development

Reporting to the Associate Principal Scientist, Process Development, the Scienti...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Bachelor’s Degree with 4+ years of experience, or Master’s Degree with 2+ years of experience, within biologics process development and manufacturing under cGMP processes
Experience with cell therapy manufacturing scale-up, technology transfer, and process development methods is required
Experience with basic biological laboratory techniques such as cell culture, PCR, cell-based bioassays, and/or ELISA
Extensive experience in flow cytometry and cell-based assays is required
Strong problem-solving skills are preferred
Experience supporting regulatory documentation, including but not limited to INDs, CTAs, and BLAs
Previous experience and working knowledge of T-cells or immunological cell therapies
Good working knowledge of cGMP manufacturing for biological processes and ICH regulations
Highly organized and efficient, with a curiosity for cutting-edge science
Strong team orientation and a passion for continuous self-development

Job Responsibility

Design and execute process development experimental plans, author associated protocols and reports, and present data and insights to cross-functional teams
Develop phase-appropriate cell therapy manufacturing processes using Quality by Design (QbD) principles
Support technology transfer of processes to CDMOs for early-phase cGMP clinical manufacturing, as needed
Contribute to the development of platform manufacturing processes and ensure readiness for clinical and future commercial manufacturing
Identify and evaluate opportunities to improve manufacturing performance, including cost, throughput, robustness, and quality
Maintain laboratory materials and sample inventory to support experimental planning and execution
Accurately document experimental data in a timely manner, ensuring data integrity, traceability, and compliance with protocols
Maintain individual training requirements in a compliant state
Contribute to regulatory filings (e.g., IND/CTA) and technical documentation, as needed
Other related duties, as assigned

What we offer

health and retirement
PTO
stock option plans

Fulltime

Associate Scientist

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States of America , South San Francisco

Salary:

110633.00 - 140020.00 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
Experience in histopathology / pathobiology in an industry setting
Hands-on experience in a variety of histology-based methodologies and equipment
Experience in documentation, including laboratory information management systems usage
Comfortable working in a dynamic environment designed to promote frequent interaction and brainstorming
Ability to manage multiple projects simultaneously
Excellent communication skills

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

Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program
stock-based long-term incentives
award-winning time-off plans
flexible work models where possible

Fulltime

Sr Associate Scientist, Cell Culture

Play a key role in advancing and optimizing autologous cell‑based therapy proces...

Location

United States , Cambridge

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Bachelor's degree in a science‑related field (Biology, Biochemistry, Biotechnology, or similar)
Hands‑on experience with aseptic cell culture and primary human immune cell culture
Working knowledge of cell therapy bioreactor systems and scale‑up concepts
Proficiency in flow cytometry and cell counting methodologies
Strong organizational skills with the ability to work effectively in fast‑paced, cross‑functional environments

Job Responsibility

Independently design, execute, and manage laboratory experiments involving primary human immune cell isolation, cell activation, genetic modification, cell expansion and cryopreservation
Apply statistical and data visualization techniques to analyze results, assess process performance, and draw data‑driven conclusions
Support process development and scale‑up efforts to translate benchtop cell culture workflows into manufacturing‑relevant processes
Perform multi‑color flow cytometry and cell‑based assays to characterize cell therapy drug products and evaluate process performance
Maintain accurate, complete, and compliant laboratory documentation in alignment with internal policies and regulatory expectations
Contribute to daily laboratory operations, continuous improvement initiatives, and feasibility assessments for new process concepts
Assist with laboratory equipment upkeep, safety practices, and general lab organization to maintain an efficient working environment

Fulltime

Select Country

Associate Scientist, Process Sciences

Job Description

Job Responsibility

Requirements

Nice to have

Looking for more opportunities?

Associate Scientist, Process Sciences

Associate Scientist, Process Sciences

Process Scientist I

Associate Scientist II, R&D, Complex Product Development

Qc Associate Scientist I

Scientist associate r&d

Scientist, Process Development

Associate Scientist

Sr Associate Scientist, Cell Culture

Our AI answers in your language