Senior Analytical Chemist Job at Advocate Group (Uxbridge)

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Senior Analytical Chemist

Senior Analytical Chemist - Advanced Mass Spectrometry Dundee | Full-Time | Per...

Location

United Kingdom , Dundee

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

A BSc, MSc or PhD in Analytical Chemistry or a related scientific discipline
Extensive practical experience using LC-MS/MS and/or GC-MS/MS (essential)
Strong experience in analytical method development and optimisation
Excellent troubleshooting and problem-solving abilities
A proven track record of producing accurate, reliable analytical data
Experience working with complex sample matrices
Strong attention to detail and commitment to scientific excellence
An interest in developing expertise within regulated laboratory environments

Job Responsibility

Develop, optimise and troubleshoot analytical methods using LC-MS/MS, GC-MS/MS and other analytical instrumentation
Analyse complex sample matrices, including oils, lipids and other challenging materials
Support method validation activities in line with industry guidelines and regulatory requirements
Ensure analytical data meets the highest standards of quality, robustness and integrity
Act as a subject matter expert for mass spectrometry across the laboratory
Troubleshoot analytical and instrumentation challenges
Contribute to laboratory process improvements and technical best practices
Support the ongoing development of quality and compliance systems within the laboratory

What we offer

Join an organisation at an exciting stage of growth and development
Be involved from the outset of a major laboratory expansion project
Work in a newly refurbished facility equipped with brand-new instrumentation
Influence laboratory processes, methods and technical direction
Develop your expertise within a supportive and collaborative environment
Work alongside talented scientists on technically challenging analytical projects
Excellent opportunity for career progression as the function continues to grow

Fulltime

Senior Quality Control Chemist

Kindeva Drug Delivery is seeking a Senior QC Chemist to join our Northridge site...

Location

United States , Northridge

Salary:

45.00 USD / Hour

Tucker Parker Smith Group

Expiration Date

Until further notice

Requirements

Bachelor's degree in Chemistry or related science
Pharmaceutical industry experience in a GMP/GXP environment
Strong knowledge of GMP/GLP requirements
Approximately 10 years of analytical testing experience
Advanced HPLC expertise
Experience leading lab investigations
U.S. Citizen or Green Card Holder
Local candidates only (no relocation)
Must pass drug and background screening

Job Responsibility

Perform analytical testing using HPLC, GC, FTIR, UV, dissolution, and other lab instrumentation
Test raw materials and finished products per USP/compendial methods and internal specifications
Prepare solutions, standards, and reagents
Lead or support laboratory investigations, deviations, and CAPA
Author and review SOPs, methods, and lab documentation
Support equipment qualification, calibration, and maintenance
Drive safety and continuous improvement initiatives

Fulltime

Senior R&D Chemist - Sorbent Innovation Lead

Senior R&D Chemist - Sorbent Innovation Lead role at Climeworks, a leading carbo...

Location

Switzerland , Opfikon, Zurich

Salary:

Not provided

Climeworks

Expiration Date

Until further notice

Requirements

Advanced degree in organic or inorganic chemistry
5+ years of experience in hands-on synthetic chemistry and material characterization
Experience in technology scouting and external innovation by setting up evaluation frameworks
Independent and results-driven work style
Strong communication and collaboration skills
Proficient in English, both spoken and written

Job Responsibility

Develop future sorbent technologies based on key performance indicators
Apply advanced analytical tools for rapid technical feasibility assessments
Identify, evaluate and prioritize next generation of sorbents available in the market
Run testing campaigns to assess sorbent potential
Ensure proper operation and maintenance of laboratory infrastructure
Protect confidential concepts and manage IP
Follow Climeworks safety rules and participate in safety exercises

What we offer

25 paid vacation days every year plus public holidays
Hybrid work setup and up to 4 weeks of remote work annually within any EU country
Fair base pay paired with an equity package
Inclusive parental leave
Dedicated budget to invest in professional growth
Referral rewards

Process Development Senior Scientist

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

Location

United States , Cambridge

Salary:

123777.00 - 167463.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD OR PharmD OR MD and relevant post-doc where applicable completed by August 2026
OR Master's degree and 3 years of Scientific experience
OR Bachelor's degree and 5 years of Scientific experience

Job Responsibility

Design and develop synthetic routes and scalable chemical processes for the manufacture of synthetic and hybrid drug substances
Develop safe, robust, efficient, and cost-effective manufacturing processes suitable for clinical and commercial production
Advance enabling technologies that accelerate pharmaceutical development and improve sustainability, efficiency, and process robustness
Support cGMP manufacturing activities and assist with technology transfer efforts to internal manufacturing sites and external contract manufacturing organizations (CMOs)
Build process understanding through experimentation, process characterization, modeling, and data analysis to ensure consistent process performance
Contribute to cross-functional drug substance development teams by providing technical expertise, experimental data, scientific recommendations, and clear documentation
Collaborate across disciplines to support regulatory filings and author technical sections of regulatory documentation
Stay current with advances in synthetic organic chemistry, process chemistry, and related technologies, and apply new scientific insights to ongoing programs
Effectively collaborate within multidisciplinary teams that include chemists, engineers, analytical scientists, and other technical experts
Independently manage project activities and deliver high-quality results within established timelines

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
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

Fulltime

Process Development Senior Scientist - Synthetic Peptides, Oligonucleotides, ADCs

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

Location

United States , Thousand Oaks

Salary:

126066.05 - 170559.95 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable]
OR Master’s degree and 3 years of Scientific experience
OR Bachelor’s degree and 5 years of Scientific experience

Job Responsibility

Work effectively with a diverse team of synthetic chemists, chemical engineers and analytical chemists to invent synthetic routes and develop safe, robust, sustainable and cost-effective processes for antibody drug conjugate, peptide antibody conjugates, synthetic peptides and/or oligonucleotide manufacturing
Drive technology innovation in the synthesis, purification, and characterization of bioconjugates, oligonucleotides, and/or synthetic peptides
Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers
Advance enabling technologies to accelerate pharmaceutical development and to improve sustainability and process efficiency
Ensure process performance through process understanding, modeling and characterization
Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc
Work cross-functionally to deliver regulatory documents and support regulatory filings
Serve as a technical expert and keep current in the field of bioconjugation, antibody drug conjugate, oligonucleotide, peptide, and process chemistry and manufacturing
Work independently in advancing projects and studies within required deadlines

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
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

Fulltime

Mea Regulatory Affairs Senior Associate

As a member of this fast-pace, complex and dynamic region, MEA Regulatory Affair...

Location

Egypt , Cairo

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Experience +2 years in Regulatory Affairs
Current/ previous experience in working as part of an MNC employer
Pharmacist, biologist, chemist-medical background
Fluent in English and Arabic for translation review purpose ( French is a huge plus)
A minimum knowledge of Middle East Africa regulatory requirements
Strong communication skills (verbal & written) with ability to understand and communicate the scientific information and anticipate/prevent potential issues
Conflict Management skillset & ability to deal with multiple stakeholders simultaneously

Job Responsibility

Deliver both strategic and administrative system support for ongoing maintenance with Lifecyle management and updates to our existing platforms and systems, to ensure data standards are 100% accurate, as to enable effective reporting and data analytics
Manage Performance Excellence through collection, analyzing & disseminating relevant information to team(s) as appropriate
Participate in local regulatory process improvements initiatives
Build newsletter, annual Report, data analysis with follow up on Key Performance Indicators and Metrics
Ensure delivery of right first time label source text for artwork creation
Support efficiently the filing plan of different marketing application submissions and products life cycle management filings by providing regional product information (leaflet and SmPC) source texts and artworks in a timely manner
Ensure implementation of master artworks as per Amgen procedures, SKU strategy and timelines with high quality to serve our patients in MENA region
Access the translation agency systems to request the label translation and track the job readiness and timelines
Perform regional prescribing information translation review: 100% review of both content and format
Perform the role of source text owner/approver and artwork reviewer/approver in the system

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Fulltime

Formulation Chemist

This role is responsible for the development and testing of new deodorant formul...

Location

United Kingdom , Leeds

Salary:

Not provided

Unilever

Expiration Date

Until further notice

Requirements

Preferably degree level in Chemistry
Some Laboratory experience in formulation
Formulation Chemistry - Understanding of ingredients
ability to modify and manipulate formulations
Evaluate and understand interactions between ingredients within formulation/process/pack through physical stability assessments
Design of experiments/protocol development
Analytical capability – analyse and interpret data
Digital skills: Data handling, analysis and interpretation of data
Information Management - knowledge capture, reporting and effective communication
Health & safety regulations and processes

Job Responsibility

Acts as the primary formulation contact at a global level, handling technical queries from various business areas including Regions, Marketing, Safety, Environmental & Regulatory Science (SERS), and Supply Chain
Communicates with multiple functional teams to help meet deadlines
Understand raw material functions and their roles in formulations
With senior WL1 guidance, adapt or create new formulas that meet product benefit and claim requirements within the formulation workstream
Be able to formulate in autonomy by planning and executing technical testing, interpreting results, troubleshoot technical issues, generating support for claims, preparing reports, communicating results to the team, and contributing towards savings initiatives
Provide supporting documentation, e.g., safety clearance, for prototype products for both internal and external testing, including consumer/claims testing
Carry out relevant qualitative and quantitative technical testing, to ensure products are fit for market/ consumer testing including specialist testing where required
Utilise Unilever software to create specifications and recipes that are used for safety and regulatory clearance and used for setting specifications for implementation into factories
To be aware of key competitors in specific to applicator area and develop formulation expertise to understand implications for Unilever products and brands
To be aware of tools for protecting intellectual property when reporting information

What we offer

competitive salary and pension scheme
annual bonus
subsidised gym membership
discounted staff shop
shares
flexible and hybrid working environment
wellbeing support including hubs, programmes and development opportunities
family-friendly and inclusive workplace

Fulltime

Ccgt operation manager

VACANCY – CCGT Power Station Operations Manager Berakas Power Company Sdn Bhd (B...

Location

Brunei Darussalam , Berakas

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Recognized Engineering Degree or equivalent qualifications and/or experience acceptable to the Company
Minimum of 5 years of demonstrated experience in a senior level position at a power station
or an equivalent combination of training and experience
In depth knowledge of CCGT power generation technology, including combustion and steam turbines, HRSG’s, ACC, water treatment plant and other general auxiliary equipment and systems
Computer literacy with Microsoft Office applications
Demonstrated leadership with excellent interpersonal, communication, negotiation, and team management skills
Proactive, pragmatic and results oriented
Evaluates own behavior and personal impact and demonstrate an adaptive management style with ability to adapt to different cultures
Proficient command of the English language, both spoken and written

Job Responsibility

Establish and recruit an Operations team, ensuring all personnel are qualified and competent – Shift Charge Engineers, Operators, Plant Chemist
Develop and implement all required operation documentation, including: Policies and Procedures, Standard Operating Procedures (SOP’s), Operation Logs and reports, Lock Out/Tag Out (LOTO) PTW system, Emergency Response procedures
Support the Owners Engineers in reviewing engineering deliverables, technical specifications, and contractor submissions
Identify and acquire all tools and test equipment required by the operations department including for the Water Treatment Plant and Lab
Manage the participation of the operations team in commissioning, performance testing, and plant start-up activities, ensuring alignment with OEM and project requirements
Ensure operational readiness for plant takeover
Lead a team of skilled operational personnel in the safe, reliable, and efficient operation of the CCGT power station
Ensure compliance with all regulatory, environmental, and safety standards
Manage the PTW system
Ensure that the plant operates at its maximum availability and reliability

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Senior Analytical Chemist

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