Analytical Operations Associate (Immunoassay) Job at Solomon Page (South San Francisco)

Sr Research Associate - Analytical Development

Theradaptive is revolutionizing the field of therapeutic delivery with a pipelin...

Location

United States , Frederick

Salary:

Not provided

Theradaptive

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Biochemistry, Pharmaceutical Analysis, Biotechnology, or Analytical Chemistry
Bachelor's degree with at least 5 years or Master's degree with at least 3 years of industry laboratory experience
Hands-on experience with Chromatography (SEC-HPLC, RP-HPLC) and/or electrophoresis (cIEF, CE-SDS) techniques
Strong multitasking abilities, effective time management skills, and excellent organizational capabilities
Ability to work collaboratively in a team environment, with meticulous attention to detail
Ability to work in a laboratory and office setting full time
Ability to lift up to 40 lbs
Ability to work in a laboratory with chemicals and biochemicals and perform Biosafety Level 2 work

Job Responsibility

Assist in the development and optimization of analytical methods using Chromatography (SEC-HPLC, RP-HPLC), moisture/water content determination (including Karl Fisher) and/or electrophoresis (cIEF, CE-SDS) techniques for the release and characterization of biologics and drug product/medical devices
Execute laboratory experiments, including sample testing and characterization of biologics using chromatography, UV spectroscopy, electrophoresis, and/or immunoassay and cell-based assays
Perform sample testing, analyze data, interpret results, and contribute to the preparation of reports in various formats, including Laboratory Notebooks (LN), formal reports, and presentations
Assist in the creation and review of Standard Operating Procedures (SOPs) for test method procedures and laboratory equipment operation and execute method qualification and validation studies
Ensure proper qualification, calibration, and maintenance of laboratory equipment in accordance with established schedules
Adhere to cGMP requirements as necessary and uphold compliance with standard operating procedures to maintain quality standards
Collaborate effectively within a team environment, demonstrate attention to detail, and communicate effectively verbally and in writing
Use standard laboratory, data analysis, and GMP quality systems, including Excel, GraphPad Prism, Laboratory Notebooks (LN), instrument software, and electronic quality systems, to support analytical development, testing, data review, investigations, trending, and compliant documentation
Adherence to laboratory and workplace safety protocols, proper use of personal protective equipment (PPE), hazard identification and reporting, and comply with the company's safety policies
Undertake any additional duties and responsibilities as needed to support the objectives of the laboratory

Fulltime

Associate Director of Operations – Immunochemistry

Mantell Associates is partnered with a global CDMO in their search for an experi...

Location

Netherlands

Salary:

Not provided

Mantell Associates

Expiration Date

Until further notice

Requirements

MSc or PhD in Biochemistry, Analytical Chemistry, Pharmacology, or a related Life Sciences discipline
Significant experience working within bioanalytical laboratories or biopharmaceutical service environments
Strong expertise in immunochemistry or immunoassay platforms, including biomarker or immunogenicity assays
Proven leadership experience managing scientific teams and operational workflows in regulated environments
Strong understanding of GLP/GCP regulatory requirements and audit/inspection readiness
Demonstrated ability to manage complex study portfolios and drive operational improvements
Excellent communication and leadership skills with the ability to engage both internal teams and external clients
Ability to work within a fast-paced CDMO environment supporting global pharmaceutical partners

Job Responsibility

Provide operational leadership for the immunochemistry department, ensuring efficient execution of bioanalytical studies and laboratory workflows
Translate strategic objectives into operational plans, managing capacity, resources, and project prioritization
Oversee laboratory performance, including planning of study activities, resource allocation, and delivery timelines
Ensure compliance with GLP/GCP standards and global regulatory expectations, maintaining strong audit and inspection readiness
Support quality systems activities including deviations, CAPAs, audit findings, and continuous improvement initiatives
Drive operational efficiency by optimizing laboratory processes, workflows, and performance metrics
Collaborate with cross-functional teams including Quality, Project Management, and Scientific Leadership to ensure successful study delivery
Provide operational input into new project proposals and support client interactions when required
Lead, mentor, and develop scientific and operational staff within the immunochemistry team
Contribute to long-term operational planning, technology evaluation, and capability development

Fulltime

Research Associate II / Senior Research Associate

We are seeking a proactive, enthusiastic candidate at the Research Associate 2 o...

Location

United States , Frederick

Salary:

89000.00 - 105000.00 USD / Year

Theradaptive

Expiration Date

Until further notice

Requirements

Bachelor's degree in Bioengineering, Biomedical Engineering, Chemistry, Biology, or a related field
Strong scientific fundamentals, analytical background, and mathematical reasoning capability
Experience designing, organizing, and executing multiple experiments and handling multiple testing activities simultaneously
Experience with bioassays, immunoassays, protein binding assays
Experience with Chromatography and Separation (e.g. SDS-PAGE) techniques
3-7 years of work experience in an industrial setting is preferred
Experience with operating under controlled procedures and documentation such as GLP or GMP is desirable
Experience with standard data analysis tools (Excel, GraphPad Prism)
Proficiency in MS Office (Word, PowerPoint, Excel)
Ability to work in a laboratory and office setting full time

Job Responsibility

Work closely with scientists and engineers to advance R&D and product development projects
Execute cell culture activities including aseptic technique, passaging, inoculations, cell differentiation, and data analysis
Execute biochemical analyses using separation techniques such as column chromatography, SDS-PAGE/CE-SDS, and RP-HPLC
Conduct a wide variety of assays, including bioassays, protein binding assays, and immunoassays
Participate in maintaining capabilities, laboratories, equipment, and supplies
Understand and adhere to laboratory safety precautions and proper use of personal protective equipment
Employ self-reliance in drawing experiment conclusions and interpreting results. Take initiative to verify the accuracy and validity of data
correct any errors
Communicate project status, roadblocks and results to supervisors and managers

Fulltime

Post-Market Compliance Specialist III- Autoimmunity

The Post-Market Compliance Specialist III supports product complaint management ...

Location

United States , San Diego

Salary:

80000.00 - 110000.00 USD / Year

werfen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in biological science, biochemistry, or similar field required
Master’s degree preferred
Proficient knowledge of IVD post-market quality system requirements and complaint handling
Advanced knowledge of global IVD post-market regulations and standards
Advanced knowledge with IVD reagents and diagnostic platforms, such as immunoassays, ELISA, chemiluminescent assays, and bead-based multiplex assays on automated systems
Advanced understanding of the functional and performance principles of IVD products, including reagents, calibrators, controls, software, and instrument systems
Minimum of six (6) years of experience in IVD industry in complaint handling, regulatory function, or a closely related technical function, required
Minimum of four (4) years of experience in Autoimmunity IVD, required
Minimum of four (4) years of hands-on laboratory testing of IVD assays including operation of automated IVD instrumentation, execution of test protocols, analysis of test results, and documentation of activities and results, required
Minimum of four (4) years of experience in customer interface responsibilities and complaint handling in an IVD regulated function, required

Job Responsibility

Complaint Management: Intakes, assesses for regulatory reportability, and triages assigned complaints. Designs and executes complex experiments and performs complex complaint investigations including investigation approach determination, experimental design, testing, analyses, and resolution. Triages investigations to other internal departments or manufacturers as needed and follows up with the escalated parties until complaint resolution. Communicates throughout the complaint investigation process from intake to final resolution with customers, affiliates, and internal stakeholders. Presents product issues which should potentially be brought to the Quality Review Board or Field Action Board to PMC management. Prepares presentations and presents issues to QRB and FARB
Laboratory Organization: Maintains laboratory cleanliness and organization. Performs routine cleaning and complete required documentation. Monitors and maintains inventory levels of laboratory test samples, consumables, reagents, and other materials. Ensures laboratory equipment and tools equipment maintenance, calibration, service, and software versions are current
Tracking and Trending: Conducts complaint trend analyses and coordinates the preparation of post-market surveillance (PMS) reports. Prepares Management Review slides on PMS for department management
Field Actions: Authors field action assessments and ensures completion of Health Hazard Evaluations (HHE/HHA) and leads recalls, Field Safety Corrective Actions (FSCAs), Field Safety Notices (FSNs), and associated regulatory notifications
Reportable Events: Completes, files and follow ups on reportable events to regulatory authorities
Department Procedures: Assists in drafting, implementing, and maintaining departmental procedures, work instructions, and templates
Provides technical guidance and mentoring to junior staff. In consultation with department management, develops and executes training for new and developing staff
Complies with applicable standard operating procedures, applicable standards and regula-tions, as well as applicable Environmental Health & Safety, Human Resources and other regulatory and administrative policies
Demonstrates Werfen values through the quality of work and professional working relationships
Other duties as assigned

What we offer

medical, dental, and vision insurance
401k plan retirement benefits with an employer match
paid vacation and sick leave
sales roles are eligible for participation in a commission plan
management and select professional roles are eligible for a performance-based bonus

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Ai Engineer

We are recruiting an AI Engineer for a direct contract with a company based in t...

Location

Portugal , Porto

Salary:

Not provided

Precise

Expiration Date

Until further notice

Requirements

2+ years experience working within a software development team as an engineer
Comfortable writing and debugging code in Python. You understand the importance of readable code and are eager to learn best practices.
Familiarity with frameworks like FastAPI, Flask, or Django, with experience developing and exposing/consuming APIs.
Understanding of containerization and exposure to Docker.
Comfortable using Git for team collaboration (Gitlab pipelines exposure is a plus).
Machine Learning Fundamentals: Foundational knowledge of ML concepts and practical experience (academic or personal projects) deploying a simple model using libraries like scikit-learn, PyTorch, or TensorFlow.
Experience manipulating and analyzing data using libraries such as Pandas and NumPy.
A strong desire to learn MLOps principles, cloud infrastructure, and deployment practices (Kubernetes exposure is a plus).
BSc in Computer Science or a related technical field.

Job Responsibility

Implementing solutions for building and deploying AI models in production, with a focus on fault tolerance, scalability, maintainability and automation.
Leveraging modern LLM’s to include/enhance parsing capabilities for CVs/job adverts for existing supported languages and new additional languages.
Collaborating with the team to design, implement and optimise data processing pipelines and evaluation tools.

Fulltime

New

Branch Manager

Come and join us as a results driven Branch Manager to deliver sales and exceed ...

Location

United Kingdom , Lymington

Salary:

Not provided

City Plumbing

Expiration Date

Until further notice

Requirements

A great positive attitude
Enjoy customer interaction
Management Experience
Safe Practices
Forward Thinking
Tenacity and resilience
A pro-active approach to sales, with a strong desire and ability to win and grow new business
Experience of customer relationship management and developing a true partnership approach
Excellent communication skills
Self confident and self motivated, with the ability to work on own initiative or as part of a wider team

Job Responsibility

Effective management of the team and resource
Setting the standard of a sales orientated culture
Delivering against sales and customer demands while maximising profitability
Maximising margin and net profit
Keeping everyone safe
Build and maintain relationships with new and existing trade and retail customers
Ability to interpret and analyse financial and statistical information

What we offer

Bonus
Discounts, savings and cash back at numerous retailers
Life assurance
Extended family policy including maternity, paternity, additional annual leave and more
Mental Health First Aiders and Employee Assistance Programme, we look out for each other
Complete induction and a company that lets you grow and encourages development
Financial education and loans
Flexible working options
A business striving to create an environment of inclusion so everyone can be their true self

Fulltime

New

Guest Environment Expert

Our jobs aren’t just about giving guests a clean room and a freshly made bed. In...

Location

United States , Poughkeepsie

Salary:

18.00 USD / Hour

Marriott Bonvoy

Expiration Date

Until further notice

Requirements

Ensuring a safe work place
following company policies and procedures
maintaining confidentiality
upholding quality standards
ensuring professional uniform, personal appearance, and communications
ability to stand, sit, or walk for an extended time
ability to move, lift, carry, push, pull, and place objects weighing less than or equal to 50 pounds without assistance

Job Responsibility

Delivering guest requests
stocking carts
cleaning rooms and public spaces
maintaining the appearance and cleanliness of the whole hotel

Parttime

New

Project Engineer

Our client is seeking a motivated and experienced Project Engineer to join their...

Location

United Kingdom , Dartford

Salary:

30000.00 GBP / Year

Office Angels

Expiration Date

Until further notice

Requirements

Proven construction based industry experience, (ideally within Smoke Ventilation/Fire Alarm Systems but not essential)
Computer literate with strong reporting and organisational skills
Excellent interpersonal and communication skills
Ability to multitask and manage cross-disciplinary projects
Strong time management and decision-making abilities
Professional, presentable, and self-motivated
Team-oriented with a commitment to exceeding client and colleague expectations
Full UK Driving License required, ideally with your own transport

Job Responsibility

Assist in the development and delivery of Risk and Method Statements
Compile detailed project reports covering quality, progress, and issues
Measuring up for install jobs and conducting Coordinate on-site deliveries to ensure smooth logistics
Support the accounts team with project-related financials and debt collection
Monitor project costs and provide financial updates, including profit/loss analysis
Communicate effectively with subcontractors and ensure alignment with project goals
Manage resources according to the client's program and track project progress
Ensure all documentation and certification is accurate, complete, and submitted on time

What we offer

23 days annual leave plus bank holidays, rising to 25 days annual leave at 2 years service
Company mobile phone
uniform and PPE
Life Insurance
Private Health Care
Pension Scheme

Fulltime

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Analytical Operations Associate (Immunoassay)

Job Description

Job Responsibility

Requirements

Nice to have

What we offer

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