Laboratory Formulation Scientist Job at Randstad (Zwijndrecht)

Sr. Formulation Scientist

JOB DESCRIPTIONDesignation: Sr. Formulation ScientistJob Location: BangaloreDepa...

Location

India , Bengaluru

Salary:

Not provided

Randstad

Expiration Date

July 17, 2026

Requirements

Master’s degree in Pharmaceutics
6 to 10 years experience in Formulation research and development - Injectable drug products
Should have knowledge regarding injectable drug products and experience in nano emulsions, suspensions, lyophilized based products, Peptides based products, non aqueous based products etc (should be experienced in atleast minimum two dosage forms)
Daily planning, execution and monitoring of experiments for the team
Knowledge and experience in handling formulation equipments like Homogenizers, Microfluidizers, lyophilizer etc
Design and implementation of products based on Quality by design principles
Integration with cross functional teams (Analytical, QA and PMO) and ability to lead the project
Maintaining stability schedules, RLDs utilization, RMs and PPMs, components inventory management
Preparation/ review of documents viz., stability protocols and reports, analytical, development studies reports, product development reports etc
Implementation/ monitoring of laboratory GLP and safety practices

Job Responsibility

Lead and execute formulation development activities for complex injectable products
Design and conduct experiments to characterize complex injectable products

Fulltime

Associate Principal Scientist - Formulation (Complex Meds)

Exciting Opportunity: Associate Principal Scientist - Formulation - Complex Meds...

Location

United Kingdom , Cheadle

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

PhD with 3+ years' of recent experience or a Bachelor's degree with 6+ years' recent experience in formulation development
Expertise in oral and parenteral formulation development, including modified-release, nano-particulate, or liposomal systems - Specifically Complex Drug Products
Strong knowledge of material properties, drug delivery systems, and global CMC regulatory requirements
Recent experience progressing complex drug products from discovery through to launch
Recent formulation experience with Peptides, Proteins, Lipids is essential
A valid UK driving licence

Job Responsibility

Leading formulation and process design for oral and parenteral drug products across clinical phases in the Complex Meds space
Applying scientific and pragmatic thinking to deliver innovative product and technology solutions
Providing hands-on troubleshooting and laboratory support when needed
Collaborating with analytical scientists to ensure robust testing of formulations
Acting as project leader for pharmaceutical development programmes
Managing CRO activities and client communications
Supporting regulatory strategy and authoring CMC documentation
Introducing new formulation technologies and contributing to continuous improvement
Coaching and mentoring junior staff and contributing to team development
Representing the company at conferences and industry events

Fulltime

R&D Formulation Scientist

The Formulation Scientist under the direction of Process Development Director is...

Location

Spain , Leon

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Master’s degree in pharmaceutics or a related scientific discipline
At least 5 years’ experience in formulation development of product formulations in solution, suspension, emulsion and lyophilized forms for small molecules and biological products, defining QTPPs and CQAs, selecting suitable form of API and designing characterization studies, compatibility, solubility, dissolution, physico-chemical stability, etc.
Good level of spoken English and Spanish
Very good written communication skills

Job Responsibility

Development of product formulations in solution, suspension, emulsion and lyophilized forms for small molecules and biological products (mAb: monoclonal antibodies
ADC: antibody drug conjugate
proteins, peptides, oligonucleotides and high potency products)
Define and update the QTPPs and CQAs of the formulation: efficacy, safety, stability, purity and potency, etc.
In partnership with the client aid in the selection of suitable form of API for final drug product through pre-formulation and formulation techniques e.g. polymorph, isomeric conformation, melting point, hygroscopicity, pH and logP, particle size
Evaluation and selection of excipients according to QTTP. Selection and concentration of the formulation excipients and definition of the CMA of the selected excipients
Design of tests to evaluate the behavior of excipients and APIs: characterization studies, compatibility, solubility, dissolution, physico-chemical stability, etc.
Application of DoE methodology to design, perform and analyze laboratory scale experiments for the optimization of formulations and their manufacturing processes
Selection, design and execution of supporting studies and documentation for the development of the project: general studies such as characterization, compatibility, robustness, stability, etc. and specific biological products studies such as freeze-thaw, shear stress, protein content, silicone compatibility, etc.
Selection of appropriate equipment, manufacturers and technologies for technical and manufacturing transfer. Perform tasks related to pre-clinical batches, including toxicological studies

What we offer

Competitive salary
Health insurance + reimbursement for medication
English classes
Discounts on various activities
Partnerships with gyms
Referral programme

Fulltime

Senior Scientist, Early Formulation Science and Drug Delivery, Drug Product Design

This position will be reporting into the Early Formulation Science and Drug Deli...

Location

United States , La Jolla

Salary:

90900.00 - 151500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Recent PhD with 0-3 year post-doctoral experience, MS with 7+ years experience, or BS with 8+ years experience in Chemistry, Chemical Engineering, Physical Chemistry, Physics, Physical Organic Chemistry, Pharmaceutics, or Pharmaceutical Sciences
Experience working independently and collaboratively in a laboratory environment

Job Responsibility

Evaluate the physicochemical properties of potential small molecule drug candidates to inform a drug product formulation strategy and developability risk assessment
Design and develop fit for purpose and diagnostic traditional and enabled formulations for preclinical studies
Design, execute, and interpret the results of polymorph and salt screens for potential drug candidates related to stability, manufacturability, and bio-performance
Apply first principles understanding of thermodynamics and kinetic processes to dissolution and precipitation of drugs in biorelevant conditions and physical and chemical stability in the solid state
Work in cross-disciplinary teams and partner with subject matter experts in Medicinal Chemistry, Pharmacokinetics & Drug Metabolism, and Clinical Pharmacology departments to influence candidate selection and progression
Develop strategic collaborations with academic and industrial researchers for addressing gaps in fundamental or applied science related to the pharmaceutical sciences
Conduct novel research and present significant findings via internal and external presentations or publications

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% of the base salary
eligibility to participate in our share based long term incentive program
Relocation support available

Fulltime

Senior Principal Scientist, Pre-Formulation and Materials Science

This Senior Principal Scientist position will be a strong scientific and leaders...

Location

United States , La Jolla

Salary:

120800.00 - 201400.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

PhD in Pharmaceutics, Pharmaceutical Sciences, Materials Science, Physical Chemistry, Physical Organic Chemistry, Biophysical Chemistry or related discipline with 10+ years relevant experience in drug delivery
BS/MS in Pharmaceutics, Pharmaceutical Sciences, Materials Science, Physical Chemistry, Physical Organic Chemistry, Biophysical Chemistry or related discipline with a minimum of 10-12 years relevant pharmaceutics industry experience in small molecule drug product design
Knowledge in biology/pharmacology/drug discovery /drug delivery up to Proof of Concept (POC) studies
Small molecule Formulation and/or early Biopharmaceutics, Materials Science, or Pharmacokinetics background
Experience in using and interpreting biophysical modeling, physicochemical (solubility & dissolution) and biological (passive, transporter mediated, efflux) transport phenomena, design, interpretation, and use of in vitro experiments, or in vivo/in vitro drug metabolism studies, and interpretation of pre-clinical exposure data for the design and selection of new small molecule drug candidates and drug delivery systems
A strong interest and motivation to learn and implement new technologies and concepts
A strong interest in leadership
Extensive practical experience working within cross-disciplinary teams and achieving results in a matrix environment
Excellent organizational and communication (oral and written) skills
The ability to work independently, as well as collaboratively

Job Responsibility

Provide scientific advances, leadership, and strategic direction for the fundamental understanding of key connectivity of molecular structure, solution and diffusion behavior and permeation characteristics to enable optimal drug formulation and drug delivery systems design
Integrates pharmaceutics, physical organic chemistry, biophysical chemistry, supramolecular chemistry, materials science, and fundamental biopharmaceutics principles into drug candidate screening and design, formulation design, solid form strategy, and ultimately project direction
Teach and mentor colleagues across the Pfizer organization
Cultivates sustainable and effective relationships with internal partners and stakeholders
Advances scientific research and expands capability in the areas of molecular design-drug delivery, materials science, early biopharmaceutics, and drug formulation

What we offer

Eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation support available

Fulltime

New

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

Analytical and Materials Scientist

Viatris is seeking an Analytical & Materials Scientist to join our Analytical Co...

Location

United Kingdom , Sandwich

Salary:

33000.00 - 37000.00 GBP / Year

SRG

Expiration Date

Until further notice

Requirements

Relevant scientific A Levels, BTEC Level 3, equivalent qualifications, or substantial practical experience
Ability to organise tasks, follow analytical methods, and deliver high‑quality results on time
Strong teamwork skills and the ability to collaborate effectively within a laboratory environment
Understanding of basic chemistry principles
Good IT skills, including Microsoft Excel, Word, and PowerPoint
Strong written and verbal communication skills
Genuine enthusiasm for working in a lab-based role
1 year of experience in industry (placement or work experience)

Job Responsibility

Conduct analytical testing to support product development, clinical trials, and regulatory submissions
Execute experiments that deepen scientific understanding in analytical and materials science, contributing to method development and formulation activities
Perform analysis related to product stability, development, and scale‑up processes
Process and interpret data, highlighting any anomalies and working with supervisors to investigate where needed
Maintain clear and accurate laboratory documentation in line with data integrity and good documentation practices
Support project delivery through additional tasks such as laboratory housekeeping, ordering, and shipment of samples
Comply with all relevant policies and procedures, including those relating to EHS, GMP, GCP, Quality, and Compliance
Undertake other duties assigned in line with the level and scope of the role

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

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Laboratory Formulation Scientist

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