Biologics Analytical Job at Randstad (苏州市)

Biologics Analytical Principal Scientist

As a Principal Scientist in Physicochemical Analysis, you will independently lea...

Location

China , 苏州市

Salary:

300000.00 - 600000.00 CNY / Year

Randstad

Expiration Date

June 28, 2026

Requirements

A Master’s degree in Analytical Chemistry, Pharmaceutical Sciences or a related field is required, with a strong technical foundation in physicochemical analysis
Profound expertise in key analytical techniques including HPLC, UPLC, LC-MS, CE and cIEF for biologics and ADC characterization is highly essential
The candidate should have 8+ years of progressive CMC experience in biopharmaceutical companies, with a proven record in method development, regulatory compliance and project leadership

Job Responsibility

Design and perform analytical support to biologics development from early to late stage
Analytical method development, transfer and troubleshooting for product quality control and stability study
Draft protocol/report and execute study to support IND/NDA filings
Participate in projects as ARD subject matter expert and provide professional guidance whenever needed

Fulltime

New

Supply Quality Manager

The Supply Quality Manager is responsible for all aspects of the Campbell Soup C...

Location

United States , Camden

Salary:

113300.00 - 155800.00 USD / Year

Campbell Soup Company

Expiration Date

Until further notice

Requirements

Bachelor's Degree required. Food Science, Food Safety, Quality, Biology, Microbiology, Supply chain, or related technical discipline
7+ years Food Safety and Quality experience. Food manufacturing experience required
Strong knowledge of supplier management and experience in ingredients and packaging categories
Ability to travel up to 50% of the time depending on supplier audits, meetings, and project needs
General computer literacy required, with proficiency in Microsoft Office software products

Job Responsibility

Leadership: Interpret, effectively communicate, and execute Supply Quality strategies, road map, objectives, and programs with cross functional and supply base partners to drive continuous improvement
Category management: Apply Food Safety and Quality management expertise on materials and processes related to a wide range of Ingredient and Packaging categories
Standards Management: Effectively write, interpret, communicate, train, and enforce Campbells policies, standards, procedures, and specifications
Risk Management: Ability to understand, interpret, and action against Food safety and Quality risk/opportunities for improvement in the Supply base management
Management of Audits: Demonstrate lead auditor skill set that includes audit planning, training auditors, performing audits, and effectively close findings by successful supplier corrective actions implementation
Management of metrics/data analytics: Demonstrate strong analytical skills with attention to detail to process information, trend, problem solve, and determine appropriate action planning
Management of performance: Effectively manage suppliers and material compliance delivered to our plants and business by using supplier nonconformance information, audits, and performance metrics
Management of Regulations: Apply deep understanding of food industry regulation with specific focus on those regulations (FDA, USDA, CFIA, and other agencies) that impact supplier food safety management
Management of Projects: Demonstrate project management skills in roles both leading projects and as an active team member
Management of people: Strong influencing and interpersonal skills that foster team building and relationship development

What we offer

Medical
dental
short and long-term disability
AD&D
life insurance
matching 401(k) plan
unlimited sick time
paid time off
holiday pay
free access to fitness center (if in WHQ)

Fulltime

New

Site Visit Report Reviewer

The Site Visit Report Reviewer (SVRR) is responsible for reviewing site qualific...

Location

India

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Excellent interpersonal, verbal and written communication skills.
Flexible and positive attitude towards work assignments and new learning.
Ability to manage multiple tasks, prioritize workload, and maintain attention to detail while committing to high-quality work.
Willingness to work in a complex environment and value teamwork.
Client-focused approach to work.
Initiative to work independently and seek guidance when necessary.
Strong analytical and decision-making skills.
Proficient in computer skills, including Microsoft Office products.
Manage time effectively and demonstrate a sense of urgency in completing tasks.
Ability to work across cultures.

Job Responsibility

Reviewing site qualification, site initiation, monitoring, and termination visit reports, ensuring they meet quality standards, regulatory requirements, Parexel Standard Operating Procedure (SOP), International Conference on Harmonization/ Good Clinical Practice (ICH/ GCP) guidelines, and protocol requirements
Working in close collaboration with Clinical Research Associates (CRAs), Clinical Operations Leaders (COLs), and project teams, the SVRR diligently monitors the progress of Open Issues, Protocol Deviations (PDs), and ongoing Serious Adverse Events (SAEs) as documented in Monitoring Visit Reports (MVRs), following up until closure
Participating in project meetings as needed
Conducting and communicating periodic analyses of monitoring visits and issues to project teams
Assisting the COL with additional tasks as required

New

Executive Director, Facilities & Engineering

Location

United States , West Greenwich

Salary:

243724.00 - 329744.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 6 years of experience in an engineering discipline or related technical field OR Master's degree and 10 years of experience in an engineering discipline or related technical field OR Bachelor's degree and 12 years of experience in an engineering discipline or related technical field AND Minimum of 6 years of managerial experience directly leading people within a multi-tiered organization and/or leading teams, projects, programs, or resource allocation activities.

Job Responsibility

Lead the organization responsible for supporting GMP manufacturing operations (24x7x365) while optimizing asset lifecycle management across the site for biologics drug substance manufacturing, warehousing, central utilities, quality control laboratories, process development laboratories, and administrative facilities
Serve as a member of the ARI Site Leadership Team (SLT)
Serve as a member of the Global Engineering Leadership Team (ELT)
Align team vision, mission, strategic objectives, and goals with ARI site priorities and Global Engineering strategies
Foster and sustain a resilient safety culture across the organization
Ensure ongoing compliance and regulatory inspection readiness
Provide technical leadership in assessing emerging industry trends and partnering with vendors to identify innovative opportunities that improve reliability, efficiency, agility, and competitive differentiation
Build and maintain strong relationships with key site and network stakeholders
Ensure active engagement and participation of the ARI site within Amgen global networks
Participate in cross-functional daily management meetings within manufacturing operations, as required

What we offer

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 and bi-annual company-wide shutdowns
Flexible work models where possible

Fulltime

New

Fellow Post Doc

The Department of Entomology seeks a Fellow Post Doc to support research on the ...

Location

United States , Manhattan

Salary:

60000.00 - 68000.00 USD / Year

Kansas State University

Expiration Date

June 17, 2026

Requirements

Requires a doctoral degree (e.g., Ph.D., Ed.D., DVM) in a field related to the assigned responsibilities

Job Responsibility

Conduct mentored research activities focused on microbial communities associated with stored product insects under the guidance of principal investigators and senior research personnel
Analyze large longitudinal datasets using R software, bioinformatics techniques, and high-performance computing systems to support research objectives and scholarly outcomes
Develop and apply analytical methodologies to interpret complex biological and microbial data
Collect, compile, organize, and maintain accurate research data and records in accordance with laboratory and sponsor requirements
Contribute to the advancement of research objectives through independent problem solving, data interpretation, and scientific analysis
Prepare peer-reviewed manuscripts, technical reports, and scholarly materials summarizing research findings related to microbial communities associated with stored product insects
Collaborate with faculty mentors, staff, and interdisciplinary research teams to refine study methodologies, data interpretation, and research outcomes
Assist with the preparation of conference materials, grant-related documents, presentations, and publication submissions
Maintain comprehensive laboratory notebook records, research documentation, and organized experimental data files
Participate in mentored professional development activities designed to strengthen research, publication, and scientific communication skills

Fulltime

New

Natural Reserve System Outreach Coordinator

The Natural Reserve System (NRS) Outreach Coordinator reports to the NRS Executi...

Location

United States , La Jolla

Salary:

55400.00 - 64000.00 USD / Year

UC San Diego

Expiration Date

June 29, 2026

Requirements

Bachelor's degree in related area such as Biology, Environmental Science, Geography, Natural Resource Management and / or equivalent experience / training
Working knowledge of departmental and organization policies and procedures
knowledge of educational program content and objectives
Working knowledge of delivering public educational programs
Working knowledge of current public education programs and trends
Working skills to produce and deliver programs
Working knowledge of conducting needs assessment
Good analytical skills to understand how business needs can be addressed through the design and delivery of training programs
Good reading, verbal, written and interpersonal communication skills, and good presentation skills. Ability to work successfully with internal and external groups. Effective written and verbal communications skills to interact with diverse groups of individuals at various organizational levels
Ability to work independently and/or with a greater team

Job Responsibility

Design, implement, and evaluate a comprehensive outreach program that leverages the four UC San Diego Natural Reserves to expand public access through guided tours, community-science workshops, and a tide-pool docent initiative
Develop curriculum-aligned field trips and author a field guide with site-specific educational modules that support K-12 and community-college educators
Formalize a 'Reserve Ambassadors' volunteer program to sustain long-term stewardship and recruit regular tide-pool docents who promote responsible ecosystem interaction
Forge strategic partnerships with local schools, community colleges, and community organizations to establish recurring visit schedules and integrate the reserves into existing educational pathways
Coordinate BioBlitz events that generate new species observations for contribution to statewide biodiversity databases
Amplify the reserves’ digital footprint by managing coordinated social-media campaigns and community-newsletter outreach

Fulltime

New

Systems Administrator, Cell Manipulation Core Facility

The System Administrator III will work internal to the Cell Manipulation Core Fa...

Location

United States , Boston

Salary:

106000.00 - 123500.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Knowledge of lab safety and infection control
Knowledge of cell therapy processing, medical, hematologic, oncologic and scientific terminology
Knowledge of Web publishing, ODBC/JDBC interfaces and SQL
Knowledgeable of BOE template builder and ability to collaborate/train on the builder
Ability to assess workload and prioritize and delegate tasks
Ability to accommodate schedule adjustments, as well as off-shift and weekend assignments as workload dictates
Excellent customer service skills and demonstrated ability to develop effective internal working relationships with a diverse employee population
Strong project management skills
Demonstrated competence in managing system projects
Demonstrated competence in writing and executing validation plans

Job Responsibility

The System Administrator III will work internal to the Cell Manipulation Core Facility to manage systems across the Cell Therapy (CT) Networks by implementation and validation of computer systems impacting the department and CT program. The System Administrator III works in conjunction with the project teams from Partners Healthcare System and CMCF technical staff as well as working with DFCI and Partners IS on enterprise systems such as Epic and Sunquest. Systems will include, but are not limited to Partners Order Entry System for Biological Products (BOE/BPAA), Eceptionist, Sunquest, REES Environmental Monitoring systems, Internal Server systems, CMCF FileMaker Databases, FreezerWorks Bio-Repository system selected MES, and other internal systems such as Microsoft Access and Filemaker databases
Demonstrates knowledge of CMCF, clinical and laboratory workflow to incorporate and propose design consideration for CMCF applications
Examines existing business models and flows of data in CT and assists to implement and support the IT manufacturing solutions for the CMCF
Performs thorough data and system analyses and develops a risk-based analysis understanding
communicates the consequences that erroneous data could have on patient care
Creates and maintains the procedures for system use, maintenance, and validation documents for upgrades and continuity of care during down time
Identifies critical data and coordinating / consolidation of existing data systems into the appropriate secure database
Manages all internal computer systems used by the facility and assists in the compilation of relevant data as required for ongoing analysis and quality improvement
Manages the team that submits data to the CIBMTR either via OTTR registry agent or formsnet3
Assists in the implementation / management of software needs for various transfusion management activities for DF clinical lab and teams

Fulltime

New

Research Associates in Photo-Biocatalysis

We are seeking motivated and collaborative individuals to join our team as Resea...

Location

United Kingdom , Manchester

Salary:

37694.00 - 46049.00 GBP / Year

The University of Manchester

Expiration Date

June 25, 2026

Requirements

PhD (or close to completion) in analytical sciences, protein science, biophysics, enzymology, structural biology, protein engineering or protein design
Experience in protein expression, purification and biochemical characterisation
Strong analytical and data-analysis skills, with confidence handling complex datasets
Ability to plan, optimise and progress research independently while working collaboratively
Excellent communication and interpersonal skills

Job Responsibility

Driving the mechanistic and structural analysis of engineered photo-biocatalysts
Producing, purifying and characterising enzyme variants and designed proteins
Designing and evaluating protein variants to understand photocatalytic function
Developing and applying advanced biophysical platforms, including light-activated and high-throughput mass spectrometry
Disseminating research through high-quality publications, reports and conference presentations

What we offer

Generous employer pension contribution
29 days annual leave plus bank holidays, along with Christmas closure
Access to world-class facilities within the Manchester Institute of Biotechnology

Fulltime

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Biologics Analytical

Job Description

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